Publications - Prof. Armin Börner
| 218. | Leidecker, Benedict N.; Peña Fuentes, Dilver; König, Matthias; Liu, Jiali; Baumann, Wolfgang; Sawall, Mathias; Neymeyr, Klaus; Jiao, Haijun; Franke, Robert; Börner, Armin; Kubis, Christoph Catalysis Science & Technology, , 14, 3966-3983. In situ spectroscopic investigations on BiPhePhos modified rhodium complexes in alkene hydroformylation. |
| 217. | Sawall, Mathias; Kubis, Christoph; Leidecker, Benedict N.; Prestin, Lukas; Andersons, Tomass; Beese, Martina; Hellwig, Jan; Franke, Robert; Börner, Armin; Neymeyr, Klaus Chemometrics and Intelligent Laboratory Systems, , 254, 105234. An automated Peak Group Analysis for vibrational spectra analysis. |
| 216. | Leidecker, Benedict N.; Fuentes, Dilver Peña; Wei, Chunhong; Sawall, Mathias; Neymeyr, Klaus; Franke, Robert; Börner, Armin; Kubis, Christoph New Journal of Chemistry, , 48, 18365-18375. In situ FTIR spectroscopic investigations on rhodium carbonyl complexes in the absence of phosphorus ligands under hydroformylation conditions. |
| 215. | Wei, Chunhong; Leidecker, Benedict N.; Peña Fuentes, Dilver; Schröder, Henning; Sawall, Mathias; Neymeyr, Klaus; Kondratenko, Evgenii V.; Börner, Armin; Franke, Robert; Kubis, Christoph Chemie Ingenieur Technik, , 96, 1657-1667. Impact of the P-Ligand Concentration on the Formation of Hydroformylation Catalysts: An in situ FTIR Spectroscopic Study. |
| 214. | Leidecker, Benedict; Spannenberg, Anke; Franke, Robert; Boerner, Armin; Kubis, Christoph IUCrData, , 8, x230083. Carbonylbis{6,6′-[(3,3′-di- tert -butyl-5,5′-dimethoxy-1,1′-biphenyl-2,2′-diyl)bis(oxy)]bis(dibenzo[ d,f ][1,3,2]-dioxaphosphepine)}hydridorhodium(I) toluene- d8 2.25-solvate. |
| 213. | Armin Boerner, Juliana Zeidler The Chemistry of Biologie. Basis and Origin of Evolution, Springer Berlin, Heidelberg, , 978-3-662-66520-6. |
| 212. | Kubis, Christoph; Koenig, Matthias; Leidecker, Benedict N.; Selent, Detlef; Schroeder, Henning; Sawall, Mathias; Baumann, Wolfgang; Spannenberg, Anke; Braecher, Alexander; Neymeyr, Klaus; Franke, Robert; Boerner, Armin ACS Catalysis, , 5245-5263. Interplay between Catalyst Complexes and Dormant States: In Situ Spectroscopic Investigations on a Catalyst System for Alkene Hydroformylation. |
| 211. | Zhang, Baoxin; Börner, Armin Nachrichten aus der Chemie, , 71, 10-15. Chinesische Schrift- und chemische Formelzeichen – eine Gegenüberstellung. |
| 210. | Boerner, Armin; Zeidler, Juliana Chemie der Biologie, Springer Spektrum Berlin, Heidelberg, , 978-3-662-64700-4. |
| 209. | Kucmierczyk, Peter; Behrens, Stephan; Kubis, Christoph; Baumann, Wolfgang; Wei, Zhihong; Jiao, Haijun; Dong, Kaiwu; Spannenberg, Anke; Neumann, Helfried; Jackstell, Ralf; Boerner, Armin; Franke, Robert; Beller, Matthias Catalysis Science & Technology, , 12, 3175-3189. (In situ) spectroscopic studies on state-of-the-art Pd(II) catalysts in solution for the alkoxycarbonylation of alkenes. |
| 208. | Zhang, Baoxin; Peña Fuentes, Dilver; Boerner, Armin ChemTexts, , 8, 2. Hydroformylation. |
| 207. | Vilches-Herrera, Marcelo; Gallardo-Fuentes, Sebastián; Aravena-Opitz, Mauricio; Yáñez-Sánchez, Mauricio; Jiao, Haijun; Holz, Jens; Boerner, Armin; Luehr, Susan The Journal of organic chemistry, , 85, 9213-9218. Reduction Over Condensation of Carbonyl Compounds Through a Transient Hemiaminal Intermediate Using Hydrazine. |
| 206. | Schroeder, Henning; Ruckebusch, Cyril; Braecher, Alexander; Sawall, Mathias; Meinhardt, Denise; Kubis, Christoph; Mostafapour, Sara; Boerner, Armin; Franke, Robert; Neymeyr, Klaus Analytica Chimica Acta, , 1137, 170-180. Reaction rate ambiguities for perturbed spectroscopic data: Theory and implementation. |
| 205. | Miró, Roger; Cunillera, Anton; Margalef, Jèssica; Lutz, Domke; Boerner, Armin; Pamiès, Oscar; Diéguez, Montserrat; Godard, Cyril , 22, 9036-9040. Rh-Catalyzed Asymmetric Hydroaminomethylation of α-Substituted Acrylamides: Application in the Synthesis of RWAY. |
| 204. | Sawall, Mathias; Kubis, Christoph; Schroeder, Henning; Meinhardt, Denise; Selent, Detlef; Franke, Robert; Braecher, Alexander; Boerner, Armin; Neymeyr, Klaus Journal of Chemometrics, , 34, e3159. Multivariate curve resolution methods and the design of experiments. |
| 203. | Sawall, Mathias; Zade, Somaye Vali; Kubis, Christoph; Schroeder, Henning; Meinhardt, Denise; Braecher, Alexander; Franke, Robert; Boerner, Armin; Abdollahi, Hamid; Neymeyr, Klaus Chemometrics and Intelligent Laboratory Systems, , 199, 103942. On the restrictiveness of equality constraints in multivariate curve resolution. |
| 202. | Holz, Jens; Wenzel, Gudrun; Spannenberg, Anke; Gandelman, Mark; Boerner, Armin Tetrahedron, , 76, 131142. New P-chirogenic tert.-butyl-xantphos ligands and their application in asymmetric hydrogenation and alkylation. |
| 201. | Kloß, Svenja; Selent, Detlef; Spannenberg, Anke; Franke, Robert; Boerner, Armin; Sharif, Muhammad Catalysts, , 9, 1036. Effects of Substitution Pattern in Phosphite Ligands Used in Rhodium-Catalyzed Hydroformylation on Reactivity and Hydrolysis Stability. |
| 200. | Leidecker, Benedict N.; Kubis, Christoph; Spannenberg, Anke; Franke, Robert; Boerner, Armin IUCrData, , 4, x191636. 6,6'-[(3,3'-Di-tert-butyl-5,5'-dimethoxy-1,1'-biphenyl-2,2'-diyl)bis(oxy)]bis(dibenzo[d,f][1,3,2]dioxaphosphepine) benzene monosolvate. |
| 199. | Selent, Detlef,; Spannenberg, Anke,; Kubis, Christoph,; Boerner, Armin, Acta Crystallographica Section C, , 75, 398-401. A dinuclear phosphite rhodium(I) complex obtained by syngas treatment of a Rh/hydroxy phosphonite olefin hydroformylation precatalyst. |
| 198. | Boerner, Armin Chemie Verbindungen fürs Leben, wbg Theiss, Darmstadt, , 978-3-8062-3884-6. |
| 197. | Levy Vahav, Heroot; Pogoreltsev, Alla; Tulchinsky, Yuri; Fridman, Natalia; Boerner, Armin; Gandelman, Mark Organometallics, , 38, 2494-2501. Synthesis and Characteristics of Iridium Complexes Bearing N-Heterocyclic Nitrenium Cationic Ligands. |
| 196. | Shuklov Ivan, A.; Shuklov Alexey, D.; Dubrovina Natalia, V.; Kuehlein, Klaus; Boerner, Armin Pure and Applied Chemistry, , 90, 285. Catalytic processes in the chemistry of lactic acid and PLLA: enzymatic stereoselective alcoholysis of rac-lactide. |
| 195. | Holz, Jens; Jiao, Haijun; Gandelman, Mark; Boerner, Armin European Journal of Organic Chemistry, , 2018, 2984-2994. About the Inversion Barriers of P‐Chirogenic Triaryl‐Substituted Phosphanes. |
| 194. | Sawall, Mathias; Moog, Annekathrin; Kubis, Christoph; Schroeder, Henning; Selent, Detlef; Franke, Robert; Braecher, Alexander; Boerner, Armin; Neymeyr, Klaus Journal of Chemometrics, , 32, Simultaneous construction of dual Borgen plots. II: Algorithmic enhancement for applications to noisy spectral data. |
| 193. | Ramon, Ruben S.; Nolan, Steven P.; Boerner, Armin; Jackstell, Ralf; Hapiot, Frederic; Monflier, Eric; Schwarze, Michael; Schomacker, Reinhard; Bergbreiter, David E.; Pilarski, Lukasz T.; Szabo, Kalman J.; Kourist, Robert; Bornscheuer, Uwe T. in New Ligands edited by Boy Cornils, ; Wolfgang A Herrmann; Matthias Beller ; Rocco Paciello , Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany, , 3, 809-950. Applied Homogeneous Catalysis with Organometallic Compounds: A Comprehensive Handbook in Four Volumes, Third Edition. |
| 192. | Cornils, Boy; Boerner, Armin; Franke, Robert; Zhang, Baoxin; Wiebus, Ernst; Schmid, Klaus in Hydroformylation edited by Boy Cornils, Wolfgang A Herrmann, Matthias Beller, Rocco Paciello, Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany, , 1, 23-90. Applied Homogeneous Catalysis with Organometallic Compounds: A Comprehensive Handbook in Three Volumes, Third Edition. |
| 191. | Morales Torres, Galina; Behrens, Stephan; Michalik, Dirk; Selent, Detlef; Spannenberg, Anke; Luehr, Susan; Dyballa, Katrin Marie; Franke, Robert; Boerner, Armin ChemistryOpen, , 6, 247-253. Synthesis of C2‐Symmetric Diphosphormonoamidites and Their Use as Ligands in Rh‐Catalyzed Hydroformylation: Relationships between Activity and Hydrolysis Stability. |
| 190. | Holz, Jens; Rumpel, Katharina; Spannenberg, Anke; Paciello, Rocco; Jiao, Haijun; Boerner, Armin ACS Catalysis, , 7, 6162-6169. P-Chirogenic Xantphos Ligands and Related Ether Diphosphines: Synthesis and Application in Rhodium-Catalyzed Asymmetric Hydrogenation. |
| 189. | Rodrigues, Claudia; Delolo, Fabio G.; Norinder, Jakob; Boerner, Armin; Bogado, André L.; Batista, Alzir A. Journal of Molecular Catalysis A: Chemical, , 426, Part B, 586-592. Hydroformylation-hydrogenation and hydroformylation-acetalization reactions catalyzed by ruthenium complexes. |
| 188. | Boerner, A.; Franke, R.; Zhang, B. in Rhodium-Based Processes edited by Cornils, B.; Hermann, W. A.; Beller, M.; Paciello, R., Wiley-VCH, Weinheim, Germany, , 26-70. Applied Homogeneous Catalysis with Organometallic Compounds. |
| 187. | Boerner, A.; Jackstell, R. in Phosphorus Ligands in Homogeneous Catalysis edited by Cornils, B.; Hermann, W. A.; Beller, M.; Paciello, R., Wiley-VCH, Weinheim, Germany, , 828-845. Applied Homogeneous Catalysis with Organometallic Compounds. |
| 186. | Holz, Jens; Doerfelt, Stephan; Boerner, Armin Advanced Synthesis & Catalysis, , 359, 4379-4387. Manufacture of Citronellal by the Rhodium-Catalyzed Homogeneous Hydrogenation of Neral. |
| 185. | Schroeder, Henning; Sawall, Mathias; Kubis, Christoph; Juerß, Annekathrin; Selent, Detlef; Braecher, Alexander; Boerner, Armin; Franke, Robert; Neymeyr, Klaus Chemometrics and Intelligent Laboratory Systems, , 163, 55-63. Comparative multivariate curve resolution study in the area of feasible solutions. |
| 184. | Sawall, Mathias; Kubis, Christoph; Barsch, Enrico; Selent, Detlef; Boerner, Armin; Neymeyr, Klaus Journal of the Iranian Chemical Society, , 13, 191-205. Peak group analysis for the extraction of pure component spectra. |
| 183. | Schroeder, Henning; Sawall, Mathias; Kubis, Christoph; Selent, Detlef; Hess, Dieter; Franke, Robert; Boerner, Armin; Neymeyr, Klaus Analytica Chimica Acta, , 927, 21-34. On the ambiguity of the reaction rate constants in multivariate curve resolution for reversible first-order reaction systems. |
| 182. | Armin Boerner, Robert Franke Hydroformylation: Fundamentals, Processes, and Applications in Organic Synthesis, Wiley-VCH, Weinheim, , 978-3-527-33552-7. |
| 181. | Zhang, Baoxin; Jiao, Haijun; Michalik, Dirk; Kloß, Svenja; Deter, Lisa Marie; Selent, Detlef; Spannenberg, Anke; Franke, Robert; Boerner, Armin ACS Catalysis, , 6, 7554-7565. Hydrolysis Stability of Bidentate Phosphites Utilized as Modifying Ligands in the Rh-Catalyzed n-Regioselective Hydroformylation of Olefins. |
| 180. | Weilbeer, Claudia; Selent, Detlef; Dyballa, Katrin Marie; Franke, Robert; Spannenberg, Anke; Boerner, Armin ChemistrySelect, , 1, 5421-5429. Evaluation of Organoselenium Based Compounds as Co-Catalysts in Rhodium-Catalyzed Hydroformylation. |
| 179. | Shuklov, I. A.; Dubrovina, N. V.; Kuehlein, K.; Boerner, A. Advanced Synthesis & Catalysis, , 358, 3910-3931. Chemo-Catalyzed Pathways to Lactic Acid and Lactates. |
| 178. | Selent, Detlef,; Spannenberg, Anke,; Boerner, Armin, IUCrData, , 1, x161914. {2-[Bis(2,4-di-tert-butylphenoxy)phosphanyloxy-κP]-3,5-di-tert-butylphenyl-κC1}{3,3'-di-tert-butyl-5,5'-dimethoxy-2,2'-bis[(1,1,2,2-tetraphenylethane-1,2-dioxy)phosphanyloxy-κP]biphenyl}rhodium(I) toluene-d8 2.7-solvate. |
| 177. | Kubis, Christoph; Profir, Irina; Fleischer, Ivana; Baumann, Wolfgang; Selent, Detlef; Fischer, Christine; Spannenberg, Anke; Ludwig, Ralf; Hess, Dieter; Franke, Robert; Boerner, Armin Chemistry – A European Journal, , 22, 2746-2757. In Situ FTIR and NMR Spectroscopic Investigations on Ruthenium-Based Catalysts for Alkene Hydroformylation. |
| 176. | Rodrigues, Claudia; Delolo, Fábio G.; Ferreira, Lucas M.; da S. Maia, Pedro I.; Deflon, Victor M.; Rabeah, Jabor; Brueckner, Angelika; Norinder, Jakob; Boerner, Armin; Bogado, André L.; Batista, Alzir A. Journal of Molecular Structure, , 1111, 84-89. Ruthenium(III)/phosphine/pyridine complexes applied in the hydrogenation reactions of polar and apolar double bonds. |
| 175. | A. Petri, A. Boerner Specialty Chemicals Magazine, , March, 26-27. Isoprene-based building blocks as flavour & fragrance intermediates. |
| 174. | Sawall, Mathias; Kubis, Christoph; Boerner, Armin; Selent, Detlef; Neymeyr, Klaus Analytica Chimica Acta, , 891, 101-112. A multiresolution approach for the convergence acceleration of multivariate curve resolution methods. |
| 173. | Torres, Galina Morales; Frauenlob, Robin; Franke, Robert; Boerner, Armin Catalysis Science & Technology, , 5, 34-54. Production of alcohols via hydroformylation. |
| 172. | Sawall, Mathias; Rahimdoust, Nahal; Kubis, Christoph; Schroeder, Henning; Selent, Detlef; Hess, Dieter; Abdollahi, Hamid; Franke, Robert; Boerner, Armin; Neymeyr, Klaus Chemometrics and Intelligent Laboratory Systems, , 149, Part A, 140-150. Soft constraints for reducing the intrinsic rotational ambiguity of the area of feasible solutions. |
| 171. | Vilches-Herrera M, Werkmeister S, Junge K, Boerner A, Beller M. CATALYSIS SCIENCE & TECHNOLOGY, 2014, 4, 629-632. Selective catalytic transfer hydrogenation of nitriles to primary amines using Pd/C. |
| 170. | Fang X, Jackstell R, Boerner A, and Beller M. CHEMISTRY – A EUROPEAN JOURNAL, 2014, 20, 15692-15696. Domino Hydroformylation/Aldol Condensation/Hydrogenation Catalysis: Highly Selective Synthesis of Ketones from Olefins. |
| 169. | Vilches-Herrera M, Domke L, Boerner A. ACS CATALYSIS, 2014, 4, 1706-1724. Isomerization-Hydroformylation Tandem Reactions. |
| 168. | Shuklov IA, Dubrovina NV, Schulze J, Tietz W, Kuehlein K, Boerner A. CHEMISTRY – A EUROPEAN JOURNAL, 2014, 20, 957-960. Propane-1,2-diols from Dilactides, Oligolactides, or Poly-L-lactic Acid (PLLA): From Plastic Waste to Chiral Bulk Chemicals. |
| 167. | Shuklov IA, Dubrovina NV, Schulze J, Tietz W, and Boerner A. TETRAHEDRON LETTERS, 2014, 55, 3495-3497. Synthesis of (R)-propane-1,2-diol from lactides by dynamic kinetic resolution. |
| 166. | Sawall M, Kubis C, Franke R, Hess D, Selent D, Boerner A, and Neymeyr K. ACS CATALYSIS, 2014, 4, 2836-2843. How To Apply the Complementarity and Coupling Theorems in MCR Methods: Practical Implementation and Application to the Rhodium-Catalyzed Hydroformylation. |
| 165. | Norinder J, Rodrigues C, and Boerner A. JOURNAL OF MOLECULAR CATALYSIS A: CHEMICAL, 2014, 391, 139-143. Tandem hydroformylation–acetalization with a ruthenium catalyst immobilized in ionic liquids. |
| 164. | Kubis C, Sawall M, Block A, Neymeyr K, Ludwig R, Boerner A, and Selent D. CHEMISTRY – A EUROPEAN JOURNAL, 2014, 20, 11921-11931. Characteristics of carbon monoxide pressure influence on monophosphite-modified olefin hydroformylation: An in situ FTIR spectroscopic and kinetic study. |
| 163. | Kubis C, Baumann W, Barsch E, Selent D, Sawall M, Ludwig R, Neymeyr K, Hess D, Franke R, Boerner A. ACS CATALYSIS, 2014, 4, 2097-2108. Catalysts for the Hydroformylation of Olefins by Combining In Situ High-Pressure FTIR and NMR Spectroscopy. |
| 162. | Gusevskaya EV, Jiménez-Pinto J, Boerner A. CHEMCATCHEM, 2014, 6, 382-411. Hydroformylation in the Realm of Scents. |
| 161. | E. Benetskiy, S. Lühr, M. Vilches-Herrera, D. Selent, H. Jiao, K. Dyballa, R. Franke, A. Börner, ACS Catal. 2014, 4, 2130-2136. Rhodium Catalyzed Non-Isomerizing Hydroformylation of Methyl Oleate Applying New Phosphoramidite Ligands. |
| 160. | M. Uhlemann, S. Doerfelt, A. Börner Tetrahedron Letters 2013, 54, 2209-2211. Rhodium Catalyzed Hydroformylation with Formaldehyde and an External H2-Source. |
| 159. | M. Sawall, C. Kubis, D. Selent, A. Börner, K. Neymeyr Journal of Chemometrics 2013, 27, 106-116. A Fast Polygon Inflation Algorithm to Compute the Area of Feasible Solutions for Three-Component Systems. I: Consepts and Applications. |
| 158. | N. V. Dubrovina, L. Domke, I. A. Shuklov, A. Spannenberg, A. Franke, A. Villinger, A. Börner Tetrahedron 2013, 69, 8809-8817. New Mono- and Bidentate P-Ligands Using One-Pot Click-Chemistry: Synthesis and Application in Rh-Catalyzed Hydroformylation. |
| 157. | Ch. Kubis, M. Sawall, A. Block, K. Neymeyr, R. Ludwig, A. Börner, D. Selent, submitted. Characteristics of carbon monoxide pressure influence on monophosphite-modified olefin hydroformylation: An in situ FTIR spectroscopic and kinetic study. |
| 156. | S. Lühr, J. Holz, O. Zayas, O. Seidelmann, L. Domke, A. Börner, Tetrahedron: Asymmetry 2013, 24, 395-401. Synthesis of enantiopure β2-homoalanine derivatives via rhodium catalyzed asymmetric hydrogenation. |
| 155. | D. Selent, A. Spannenberg, A. Börner, Acta Cryst. 2013, E69, m14. Carbonyl {3,3'-di-tert-butyl-5,5'-dimethoxy-2,2'-bis[(4,4,5,5-tetramethyl-1,3,2-dioxaphospholan-2-yl)oxy]biphenyl-κ2P,P'}hydrido(triphenylphosphane-κP)rhodium(I) diethyl ether trisolvate. |
| 154. | K. N. Gavrilov, A. A. Shiryaev, I. V. Chuchelkin, S. V. Zheglov, E. A. Rastorguev, V. A. Davankov, A. Börner, Tetrahedron: Asymmetry 2012, 23, 1052-1057. BINOL-Derived Diphosphoramidites bearing Unsymmetrical 1,2-Diamine Link and their Application in Asymmetric Catalysis. |
| 153. | I. A. Shuklov, N. V. Dubrovina, J. Schulze, W. Tietz, K. Kühlein, A. Börner, Tetrahedron Lett. 2012, 53, 6326–6328. Ruthenium- and lipase-catalyzed inversion of L-lactates. |
| 152. | Ch. Kubis, D. Selent, M. Sawall, R. Ludwig, K. Neymeyr, W. Baumann, R. Franke, A. Börner, Chem. Eur. J. 2012, 18, 8780-8794. Exploring Between the Extremes: Conversion-Dependent Kinetics of Phosphite-Modified Hydroformylation Catalysis. |
| 151. | S. Lühr, J. Holz, O. Zayas, V. Wendisch, A. Börner, Tetrahedron: Asymmetry 2012, 23, 1301-1319. Synthesis of chiral β2-amino acids by asymmetric hydrogenation. |
| 150. | M. Sawall, A. Börner, C. Kubis, D. Selent, R. Ludwig, K. Neymeyr, J. Chemometrics 2012, 26, 538-548. Model-free multivariate curve resolution with model-based kinetics: algorithm and applications. |
| 149. | D. Selent, A. Spannenberg, A. Börner, Acta Cryst. 2012, E 68, m488. Dicarbonyl{3,3’-di-tert-butyl-5,5’-dimethoxy-2,2’-bis-[(4,4,5,5-tetraphenyl-1,3,2-dioxaphospholan-2-yl)oxy-κP]biphenyl hydridorhodium(I) diethyl ether monosolvate. |
| 148. | M. Uhlemann, A. Börner, ChemCatChem 2012, 4, 753-754. A Highly Enantioselective Rh-Catalyzed Hydroformylation of α-Alkylacrylates. |
| 147. | D. Selent, A. Spannenberg, A. Börner, Acta Cryst. 2012, E 68, m215. {2-[Bis(2,4-di-tert butylphenoxy)phosphanyloxy-[κ]P]-3,5-di-tert-butylphenyl-[κ]C^[1]}[(1,2,5,6-[ε])-cycloocta-1,5-diene]-rhodium(I)toluene monosolvate. |
| 146. | S. P. Verevkin, V. N. Emel’yanenko, J. Bayardon, W. Baumann, B. Schäffner, A. Börner, Ind. Eng. Chem. Res. 2012, Ind. Eng. Chem. Res. 2012, 51, 126-132. Asymmetric Hydrogenation of Non Functionalized Olefins in Propylene Carbonate – Kinetic or Thermodynamic Control? |
| 145. | S. Erfle, T. Rahn, F. Bendrath, W. Baumann, D. Michalik, H. J. Jiao, A. Spannenberg, A. Boerner, P. Langer, Tetrahedron 2011, 67, 8780-8789. Synthesis and Characterization of Permethylated 1,3,5-Tri- and 1,3,5,7-Tetracarbonyl Compounds. |
| 144. | I. A. Shuklov, N. V. Dubrovina, J. Schulze, W. Tietz, K. Kühlein, A. Börner, ARKIVOC 2012, (iii), 66-75. Promoters for Pd-catalyzed methoxycarbonylation of vinyl acetate. |
| 143. | D. Selent, R. Franke, A. Spannenberg, W. Baumann, B. Kreidler, A. Börner, Organometallics 2011, 30, 4509-4514. A New Diphosphite Promoting Highly Regioselective Rhodium-Catalyzed Hydroformylation. |
| 142. | T. Rahn, F. Bendrath, M. Hein, W. Baumann, H. Jiao, A. Börner, A. Villinger, P. Langer, Org. Biomol. Chem. 2011, 9, 5172-5184. Synthesis and characterization of bis-cyclopropanated 1,3,5-tricarbonyl compounds. A combined synthetic, spectroscopic and theoretical study. |
| 141. | J. Norinder, A. Börner, Chemcatchem 2011, 3, 1407-1409. Highly Efficient and Selective Catalytic N-Alkylation of Amines with Alcohols in Water. |
| 140. | I. S. Mikhel, N. V. Dubrovina, I. A. Shuklov, W. Baumann, D. Selent, H. J. Jiao, A. Christiansen, R. Franke, A. Börner, Journal of Organometallic Chemistry 2011, 696, 3050-3057. Synthesis, Complexation Behavior and Application of a new Diphosphite Ligand in Rhodium-Catalyzed Hydroformylation. |
| 139. | S. Luehr, J. Holz, A. Börner, Chemcatchem 2011, 3, 1708-1730. The Synthesis of Chiral Phosphorus Ligands for Use in Homogeneous Metal Catalysis |
| 138. | I. Karame, G. Nemra-Baydoun, R. Abdallah, A. Kanj, A. Börner, Synthetic Communicatins 2011, 41, 583-588. Highly Regioselective Synthesis of Ethyl 2-(N-Methylformate-1,4,5,6-Tetrahydropyridin-2-yl) Acetate and its Conversion into Corresponding (R)-Ethyl Homopepicolate by Asymmetric Hydrogenation. |
| 137. | A. Christiansen, D. Selent, A. Spannenberg, M. Koeckerling, H. Reinke, W. Baumann, H. J. Jiao, R. Franke, A. Börner Chemistry – A European Journal 2011, 17, 2120-2129. Heteroatom-Substituted Secondary Phosphine Oxides (HASPOs) as Decomposition Products and Preligands in Rhodium-Catalysed Hydroformylation. |
| 136. | I. Shuklov, H. Jiao, J. Schulze, W. Tietz, K. Kühlein, A. Börner, Tetrahedron Lett. 2011, 52, 1027-1030. Studies on the Epimerisation of Diastereomeric Dilactides. |
| 135. | I. Karamé, G. Nemra-Baydoun, R. Abdallah, A. Kanj, A. Börner, Synth. Commun. 2011, 41, 583-588. Highly regioselective synthesis route of ethyl 2-(N-methylformate-1,4,5,6-tetrahydropyridin-2-yl) acetate and its conversion into corresponding (R)ethyl homopepicolate by asymmetric hydrogenation. |
| 134. | B. Schaeffner, F. Schaeffner, S. P. Verevkin, A. Boerner, Chemical Reviews 2010, 110, 4554-4581. Organic Carbonates as Solvents in Synthesis and Catalysis. |
| 133. | A. Christiansen, Ch. Li, M. Garland, D. Selent, R. Ludwig, R. Franke, A. Börner, ChemCatChem, 2010, 2, 1278-1285.. Secondary Phosphane Oxides (SPOs) as Preligands in the Rhodium Catalyzed Hydroformylation. |
| 132. | A. Christiansen, D. Selent, A. Spannenberg, W. Baumann, R. Franke, A. Börner, Organometallics, 2010, 29, 3139-3145. Reaction of Secondary Phosphine Oxides with Rhodium(I). |
| 131. | N. Andrushko, V. Andrushko, Peter Roose, K. Moonen, A. Börner, ChemCatChem 2010, 2, 640-643. Amination of Aliphatic Alcohols and Diols with an Ir-Pincer Catalyst. |
| 130. | A. Christiansen, Ch. Li, M. Garland, D. Selent, R. Ludwig, A. Spannenberg, W. Baumann, A. Börner, Eur. J. Org. Chem. 2010, 2733-2741. On the Tautomerism of Secondary Phosphane Oxides. |
| 129. | K. N. Gavrilov, E. B. Benetsky, V. E. Boyko, E. A. Rastorguev, V. A. Davanko, B. Schaeffner, A. Boerner, Chirality 2010, 22, 844-848. (S)-6-Bromo-BINOL-Based Phosphoramidite Ligand wit C1 Symmetry for Enantioselective Hydrogenation and Allylic Substitution. |
| 128. | I. A. Shuklov, N. V. Dubrovina, H. Jiao, A. Spannenberg, A. Börner, Eur. J. Org. Chem. 2010, 1669-1680. A Highly Diastereoselective Route to Dinaphtho[c,e][1,2]oxaphosphorines and their Application as Ligands in Homogeneous Catalysis. |
| 127. | C. Kubis, R. Ludwig, M. Sawall, K. Neymeyr, A. Börner, K.-D. Wiese, D. Hess, R. Franke, D. Selent, ChemCatChem 2010, 2, 287-295. A comparative in situ HP-FTIR spectroscopic study of bi- and monodentate phosphite modified hydroformylation. |
126. | N. Andrushko, V. Andrushko, V. Tararov, A. Korostylev, G. König, A. Börner, Chirality 2010, 22, 534-541. Highly Stereoselective Hydrogenations – as Key-Steps in the Total Synthesis of Statins. |
| 125. | F. Shi, M. K. Tse, S. Zhou, M.-M. Pohl, J. Radnik, S. Hübner, K. Jähnisch, A. Brückner and M. Beller J. Am. Chem. Soc. 2009, 131, 1775-1779. Green and Efficient Synthesis of Sulfonamides Catalyzed by Nano-Ru/Fe3O4. |
| 124. | B. Schaeffner, S. P. Verevkin, A. Boerner, Chemie In Unserer Zeit 2009, 43, 12-21. Gruene Loesungsmittel fuer Synthese und Katalyse. |
| 123. | K. N. Gavrilov, S. V. Zheglov, E. B. Benetsky, A. S. Safronov, E. A. Rastorguev, N. N. Groshkin, V. A. Davankov, B. Schäffner, A. Börner, Tetrahedron: Asymmetry 2009, 20, 2490-2496. P*,P*- Bidentate diastereoisomeric bisdiamidophosphites based on N-benzyltartarimide and their applications in asymmetric catalytic processes. |
| 122. | K. N. Gavrilov, E. B. Benetskiy, T. B. Grishina, E. A. Rastorguev, M. G. Maksimova, S. V. Zheglov, V. A. Davankov, B. Schäffner, A. Börner, S. Rosset, G. Bailat, A. Alexakis, Eur. J. Org. Chem. 2009, 3923-3929. Bulky P*-Chirogenic Diazaphospholidines as Monodentate Ligands for Asymmetric Catalysis. |
| 121. | J. Mazuela, J. J. Verendel, M. Coll, B. Schäffner, A. Börner, P. G. Anderson, O. Pàmies, M. Diéguez, J. Am. Chem. Soc. 2009, 131, 12344-12353. Iridium phosphite-oxazoline catalysts for the highly enantioselective hydrogenation of terminal alkenes. |
| 120. | T. Rahn, B. Appel, W. Baumann, H. Jiao, A. Börner, C. Fischer, P. Langer, Org. Biomol. Chem. 2009, 7, 1931-1938. Synthesis of chromones and 4-hydroxyquinolines based on uncatalyzed condensations of 1-methoxy-1,3-bis(trimethylsilyloxy)-1,3-butadiene with 2-alkoxy- and 2-nitrobenzoyl chlorides and related reactions. |
| 119. | B. Schäffner, V. Andrushko, J. Bayardon, J. Holz, A. Börner, Chirality 2009, 21, 857-861. Organic Carbonates as Alternative Solvents for Asymmetric Hydrogenation. |
| 118. | I. A. Shuklov, N. V. Dubrovina, E. Barsch, R. Ludwig, D. Michalik, A. Börner, Chem. Commun. 2009, 1535-1537. Solvent dependent asymmetric hydrogenation with self-assembled catalysts: a combined catalytic, NMR- and IR-study. |
| 117. | T. Schulz, Ch. Torborg, S. Enthaler, B. Schäffner, A. Dumrath, A. Spannenberg, H. Neumann, A. Börner, M. Beller, Chem. Eur. J. 2009, 15, 4528-4533. A General Palladium-catalyzed Amination of Aryl Halides with Ammonia. |
| 116. | Ch. Torborg, J. Huang, T. Schulz, B. Schäffner, A. Zapf, A. Spannenberg, A. Börner, M. Beller, Chem. Eur. J. 2009, 15, 1329-1336. Improved palladium-catalyzed Sonogashira coupling reactions of aryl chlorides. |
| 115. | T. Schulz, Ch. Torborg, B. Schäffner, J. Huang, A. Zapf, R Kadyrov, A. Börner, M. Beller, Angew. Chem. 2009, 121, 936-939; Angew. Chem. Int. Ed. 2009, 48, 918-921. Practical new Imidazole-based Phosphine Ligands for Selective Palladium-catalyzed Hydroxylation of Aryl Halides. |
| 114. | M. Sebek, J. Holz, A. Börner, K. Jähnisch, Synlett 2009, 461-465. Highly Diastereoselective Hydrogenation of Furan-2-carboxylic Acid Derivatives on Heterogeneous Catalysts. |
| 113. | K. N. Gavrilov, C. W. Shezlov, P. A. Wolozshanin, E. A. Rasmorzuev, A. A. Shirjaev, M. G. Maksimova, C. E. Ljubimov, J. B. Benzkii, A. Z. Zafronov, P. W. Pemprovskii, B. A. Davankov, B. Schäffner, A. Börner, Isv. Akad. Nauk, Ser. Chim. 2008, 2266-2274. Diastereomeric P*- mono and P*,P*-bidentate diaminophosphite ligands on the basis of 1,4:3,6-dianhydro-D-mannitol in asymmetric metal catalyzed reactions. |
| 112. | D. Selent, W. Baumann, K.-D. Wiese, A. Börner, Chem. Commun. 2008, 6203–6205. Diastereoisomeric Bisphosphite Ligands in the Hydroformylation of Octenes: Rhodium Catalysis and HP-NMR investigations. |
| 111. | J. Holz, B. Schäffner, O. Zayas, A. Spannenberg, A. Börner, Adv. Synt. Catal. 2008, 350, 2533-2543. Synthesis of Chiral 2-Hydroxy-1-methylpropanoates by Rhodium-catalyzed Stereoselective Hydrogenation of a-(Hydroxymethyl)-acrylate Derivatives. |
| 110. | B. Schäffner, V. Andrushko, S. P. Verevkin, J. Holz, A. Börner, ChemSusChem. 2008, 1, 934-940. Rh-Catalyzed Asymmetric Hydrogenation of Unsaturated Lactate Precursors in PC. |
| 109. | K. N. Gavrilov, S. V. Zheglov, P. A. Vologzhanin, E. A. Rastorguev, A. A. Shiryaev, M. G. Maksimova, S. E. Lyubimov, E. B. Benetsky, A. S. Safronov, P. V. Petrovskii, V.A. Davankov, B. Schäffner, A. Börner. Izvestiya Akademii Nauk. Ser. Khim. 2008, No. 11, 2264–2272. Diastereomeric P*-mono and P*,P*-bidentate diamidophosphite ligands with 1,4:3,6-dianhydro-D-mannite backbone in asymmetric metal-complex catalysis. |
| 108. | N. Andrushko, V. Andrushko, T. Thyrann, G. König, A. Börner,Tetrahedron Lett. 2008, 49, 5980-5982. Synthesis of enantiopure (R)-2-(4-methoxy-3-(3-methoxypropoxy)-benzyl)-3-methylbutanoic acid a key intermediate for the preparation of Aliskiren. |
| 107. | S. P. Verevkin, V. N. Emel’yanenko, A. V. Toktonov, Y. Chernyak, B. Schäffner, A. Börner, J. Chem. Thermodyn. 2008, 40, 1428-1432. Cyclic Alkylene Carbonates. Experiment and First Principles Calculations for Prediction of Thermochemical Properties. |
| 106. | V. Andrushko, N. Andrushko, G. König, A. Börner, Tetrahedron Lett. 2008, 49, 4836-4839. Highly enantioselective catalytic hydrogenation of a 5-amino-3,5-dioxopentanoic ester. |
| 105. | S. P. Verevkin, V. N. Emel’yanenko, A. V. Toktonov, Y. Chernyak, B. Schäffner, A. Börner, Fluide Phase Equilibria 2008, 268, 1-6. Cyclic Alkylene Carbonates. Experiment and First Principles Calculations for Prediction of Thermochemical Properties. |
| 104. | R. Kadyrov, J. Holz, B. Schäffner, O. Zayas, J. Almena, A. Börner, Tetrahedron: Asymmetry 2008, 19, 1189-1192. Synthesis of Chiral b-Aminophosphonates via Rh-Catalyzed Asymmetric Hydrogenation of b-Amido-vinylphosphonates. |
| 103. | S. A. Kozlova, V. N. Emel’yanenko, M. Georgieva, S. P. Verevkin, Y. Chernyak, B. Schäffner, A. Börner, J. Chem. Thermodyn. 2008, 40, 1136-1140. Aliphatic Alkyl Carbonates. Vapour Pressures at Ambient Temperatures. |
| 102. | K. N. Gavrilov, S. V. Zheglov, P. A. Vologzhanin, M. G. Maksimova, A. S. Safronov, S. E. Lyubimov, V. A. Davankov, B. Schäffner, A. Börner. P*-chiral bisdiamidophosphite ligand with 1,4:3,6-dianhydro-D-mannite backbone and its application in asymmetric catalysis. Tetrahedron Lett. 2008, 49, 3120-3123. |
| 101. | V. N. Emelyanenko, A. V. Toktonov, S. A. Kozlova, S. P. Verevkin, V. Andrushko, N. Andrushko, A. Börner, J. Phys. Chem. A, 2008, 112, 4036-404. Structure-Energy Relationships in Unsaturated Esters of Carboxylic acids. Thermochemical Measurements and Ab Initio Calculations. |
| 100. | B. Schäffner, J. Holz, S. P. Verevkin, A. Börner, ChemSusChem 2008, 249-253. Organic Carbonates as Alternative Solvent for Palladium-catalyzed Substitution Reactions. |
| 99. | B. Schäffner, J. Holz, S. P. Verevkin, A. Börner, Tetrahedron Lett. 2008, 49, 768-771. Rhodium-catalyzed asymmetric hydrogenation with self-assembling catalysts in propylene carbonate. |
| 98. | I. D. Kostas, K. A. Vallianatou, J. Holz, A. Börner, Tetrahedron Lett. 2008, 49, 331-334. A new very easily accessible chiral phosphite-phosphoramidite ligand based on 2-anilinoethanol and R-BINOL moieties for Rh-catalyzed asymmetric olefin hydrogenation. |
| 97. | N. Andrushko, V. Andrushko, G. König, Anke Spannenberg, A. Börner, Eur. J. Org. Chem. 2008, 847-853. A New Approach to the Total Synthesis of Rosuvastatin. |
| 96. | A. Korostylev, V. Andrushko, N. Andrushko, V. I. Tararov, G. König, A. Börner, Eur. J. Org. Chem. 2008, 840-846. Highly Enantioselective Hydrogenation of Ethyl 5,5-Dimethoxy-3-oxopentanoate and its Application for the Synthesis of a Statin Precursor. |
| 95. | A. Preetz, H.-J. Drexler, C. Fischer, Z. Dai, A. Börner, W. Baumann, A. Spannenberg, R. Thede, D. Heller, Chem. Eur. J. 2008, 1445-1451. Rhodium complex catalyzed asymmetric hydrogenation - Transfer of pre-catalysts into active specie. |
| 94. | M.-N. Birkholz, N. V. Dubrovina, I. A. Shuklov, J. Holz, R. Paciello, Ch. Waloch, B. Breit, A. Börner, Tetrahedron: Asymmetry 2007, 18, 2055-2060. Enantioselective Pd-catalyzed allylic amination with self-assembling and non-assembling monodentate phosphine ligands. |
| 93. | N. V. Dubrovina, I. A. Shuklov, M.-N. Birkholz, D. Michalik, R. Paciello, A. Börner, Adv. Synth. Catal. 2007, 349, 2183-2187. Fluorinated Alcohols as Solvents for Enantioselective Hydrogenation with Chiral Self-Assembling Rh-Catalysts. |
| 92. | J. Bayardon, J. Holz, B. Schäffner, V. Andrushko, S. Verevkin, A. Preetz, A. Börner, Angew. Chem. 2007, 119, 6075-6078; Angew. Chem. Int. Ed. 2007, 46, 5971-5974. Propylencarbonat - Ein neues Lösungsmittel für die asymmetrische Hydrierung. |
| 91. | J. Holz, A. Börner, D. Heller, H.-J. Drexler, Crystal structure of (2,3)-bis(2R,5R)-2,5-dimethylphosphanyl)maleic anhydride)-(μ4-norbornadiene)-rhodium(I) tetrafluoroborate [Rh(C7H8)(C16H24O3P2][BF4] Z. Kristall. NCS 2007, 222, 463-464. |
| 90. | I. Karamé, E. Bellur, S. Rotzoll, P. Langer, C. Fischer, J. Holz, A. Börner, Synth. Commun. 2007, 37, 1067-1076. Highly Enantioselective Hydrogenation of β-Alkyl and β-(w-Chloroalkyl) Substituted β-Keto Esters. |
| 89. | M.-N. Gensow, N. V. Dubrovina, H. Jiao, D. Michalik, J. Holz, R. Paciello, B. Breit, A. Börner, Chem. Eur. J. 2007, 13, 5896-5907. Enantioselective Hydrogenation with New Self-Assembling Rh-Phosphane Catalysts – Influence of Ligand structure and solvent. |
| 88. | S. Enthaler, G. Erre, K. Junge, J. Holz, A. Börner, E. Alberico, I. Nieddu, S. Gladiali, M. Beller, Org. Proc. Res. Dev. 2007, 11, 568-577. Development of Practical Rhodium Phosphine Catalysts for the Hydrogenation of b–Dehydroamino Acid Derivates. |
| 87. | J. Holz, A. Monsees, R. Kadyrov, A. Börner, Synlett 2007, 599-603. Chiral P-Chlorophospholane – a Versatile Building Block for the Synthesis of Ligands,. |
| 86. | V. Bilenko, H. Jiao, A. Spannenberg, C. Fischer, H. Reinke, J. Kösters, I. Komarov, A. Börner, Eur. J. Org. Chem. 2007, 758-767. A New Target for Highly Stereoselective Katsuki-Sharpless-Epoxidation - One-Pot Synthesis of C2-Symmetric 2,2'-Bisoxiranes. |
| 85. | V. I. Tararov, N. Andrushko, V. Andrushko, G. König, A. Spannenberg, A. Börner, Eur. J. Org. Chem. 2006, 5543-5550. From Ethyl (3R,5S)-5,6-(isopropylidenedioxy)-3-hydroxyhexano-ate to the Chiral Side Chain of Statins - Lactone versus Lactol Pathway. |
| 84. | V. I. Tararov, G. König, A. Börner, Adv. Synth. Catal. 2006, 348, 2633-2644. Synthesis and Highly Stereoselective Hydrogenation of the Statine Precursor Ethyl (5S)-5,6-Isopropylidenedioxy-3-oxohexanoate. |
| 83. | D. Kostas, K. A. Vallianatou, J. Holz, A. Börner, Tetrahedron Lett. 2006, 47, 7947-7950. Me-AnilaPhos - A New Chiral Phosphine-Phosphoramidite Ligand for Highly Efficient Rh-catalyzed Asymmetric Olefin Hydrogenation. |
| 82. | V. Bilenko, A. Spannenberg, W. Baumann, I. Komarov, A. Börner, Tetrahedron: Asymmetry 2006, 17, 2082-2087. A New Chiral Monodentate Phospholane Ligands by Highly Stereoselective Hydrophosphination. |
| 81. | N. V. Dubrovina, H. Jiao, V. I. Tararov, A. Spannenberg, R. Kadyrov, A. Monsees, A. Christansen, A. Börner, Eur. J. Org. Chem. 2006, 3412-3420. A New Access to Chiral Phospholanes. |
| 80. | J. Holz, O. Zayas, H. Jiao, W. Baumann, A. Spannenberg, A. Monsees, T. H. Riermeier, J. Almena, R. Kadyrov, A. Börner, Chem. Eur. J. 2006, 12, 5001-5013. A Highly Tunable Family of Chiral Bisphospholanes for Rh-Catalyzed Enantioselective Hydrogenation. |
| 79. | V. I. Tararov, A. Korostylev, G. König, A. Börner, Synth. Commun. 2006, 36, 187-191. Facile Preparation and Purification of Mono t-Butyl Malonate. |
| 78. | D. Selent, K.-D. Wiese, A. Börner, O-Acylphosphites: New and promising ligands for isomerising hydroformylation, In Cat. Org. React., Hrsg. J. R. Sowa Jr., Taylor & Francis, Boca Raton, 2005, 459-469. |
| 77. | N. V. Dubrovina, V. I. Tararov, A. Monsees, A. Spannenberg, I. D. Kostas, A. Börner, Tetrahedron: Asymmetry 2005, 16, 3640-3649. New chiral 1,3-diphosphine ligands for Rh-catalyzed enantioselective hydrogenation: a search for electronic effects. |
| 76. | I. D. Kostas, K. A. Vallianatou, J. Holz, A. Börner, Appl. Organomet. Chem. 2005, 19, 1090-1095. Rhodium complexes with a new chiral nitrogen-containing BINOL-based diphosphite or phosphonite ligand. Synthesis and application to hydroformylation of styrene and/or hydrogenation of prochiral olefins. |
| 75. | N. V. Dubrovina, A. Börner, Angew. Chem. 2004, 116, 6007-6010. Angew. Chem. Int. Ed. 2004, 43, 5883-5886. Enantioselektive Katalysen mit chiralen Phosphanoxid-Präliganden. |
| 74. | V. I. Tararov, R. Kadyrov, C. Fischer, A. Börner, Synlett 2004,1961-1962. Selective N-Benzylation of Amino Acids under Homogeneously Catalyzed Hydrogenation Conditions. |
| 73. | N. V. Dubrovina, V. I. Tararov Z. Kadyrova, A. Monsees, A. Börner, Synthesis 2004, 2047-2051. Versatile Synthesis of Chiral Aminophosphine Phosphinites (AMPPs) as Ligands for Enantioselective Hydrogenation. |
| 72. | J. Almena, A. Monsees, R. Kadyrov, T. Riermeier, B. Gotov, J. Holz, A. Börner, Adv. Synth. Catal. 2004, 346, 1263-1266. Asymmetric Hydrogenation of Itaconic Acid Derivatives with the New CatASium® M Catalysts. |
| 71. | J. Holz, A. Börner, A. Spannenberg, C. Pribbenow, D. Heller, H.-J. Drexler, Z. Kristall. NCS 2004, 219, 199-200. |
| 70. | T. H. Riermeier, A. Monsees, J. Holz, A. Börner, Chimia Oggi, 2004, 22-24. catASium®M - A new family of chiral bisphospholanes and their application in enantioselective hydrogenations. |
| 69. | A. Korostylev, V. Tararov, Ch. Fischer, A. Monsees, A. Börner, J. Org. Chem. 2004, 3220-3221. A Convenient and Efficient Reduction of 1,1'-Binaphthyls to H8-1,1'-Binaphthyl Derivatives with Pd and Ru Catalysts on Solid Support. |
| 68. | V. I. Tararov, R. Kadyrov, T. H. Riermeier, C. Fischer, A. Börner, Adv. Synth. Catal. 2004, 346, 561-565. Direct Reductive Amination versus Hydrogenation of Intermediates – A Comparison. |
| 67. | A. Korostylev, A. Monsees, C. Fischer, A. Börner, Tetrahedron: Asymmetry 2004, 15, 1001-1005. BINOL Derived Monodentate Acylphosphite Ligands for Homogeneously Catalyzed Enantioselective Hydrogenations. |
| 66. | D. Selent, W. Baumann, R. Kempe, A. Spannenberg, D. Röttger, K.-D. Wiese, A. Börner, Organometallics 2003, 22, 4265-4271. Reactions of a Hydroxy Phosphonite Ligand in the Coordination Sphere of Rhodium(I). |
| 65. | N. V. Dubrovina, V. I. Tararov, A. Monsees, J. Almena, R. Kadyrov, A. Börner, Tetrahedron: Asymmetry 2003, 14, 2739-2745. On the Economic Preparation of a Versatile Chiral Diphosphine Ligand for Enantioselective Hydrogenations. |
| 64. | I. V. Komarov, A. Spannenberg, J. Holz, A. Börner, Chem. Commun. 2003, 2240-2241. Highly stereoselective, thermodynamically controlled and reversible formation of a new P-chiral phosphine. |
| 63. | A. Korostylev, D. Selent, A. Monsees, C. Borgmann, A. Börner, Tetrahedron: Asymmetry 2003, 14, 1905-1909. Chiral Pyrophosphites - A New Class of Organophosphorus Ligands, Synthesis and Application in Rh(I) Catalyzed Asymmetric Hydrogenation. |
| 62. | R. Kadyrov, T. H. Riermeier, U. Dingerdissen, V. Tararov, A. Börner, J. Org. Chem. 2003, 68, 4067. The First Highly Enantioselective Homogeneously Catalyzed Asymmetric Reductive Amination: Synthesis of N-Benzylamino Acids. |
| 61. | V. I. Tararov, R. Kadyrov, A. Monsees, T. H. Riermeier, A. Börner, Adv. Synth. Catal. 2003, 345, 239. Asymmetric Cleavage of Racemic 1,3-Oxazolidines - A New Dynamic Process in Homogeneous Rh(I) Catalyzed Hydrogenation. |
| 60. | J. Holz, A. Monsees, H. Jiao, J. You, I. V. Komarov, C. Fischer, K. Drauz, A. Börner, J. Org. Chem. 2003, 68, 1701. Synthesis of a New Chiral Bisphospholane Ligand for the Rh(I) Catalyzed Enantioselective Hydrogenation of Isomeric β-Acylamido Acrylates. |
| 59. | D. Heller, J. Holz, I. Komarov, H.-J. Drexler, J. You, K. Drauz, A. Börner, Tetrahedron: Asymmetry 2002, 13, 2735. On the Enantioselective Hydrogenation of Isomeric β-Acylamido β-Alkylacrylates with Chiral Rh(I) Complexes - Comparison of Phosphine Ligands and Substrates. |
| 58. | I. V. Komarov, A. Monsees, A. Spannenberg, W. Baumann, U. Schmidt, C. Fischer, A. Börner, Eur. J. Org. Chem. 2002, 138. Chiral oxy-functionalized diphosphane ligands derived from camphor for rhodium(I) catalyzed enantioselective hydrogenation. |
| 57. | I. V. Komarov, A. Monsees, R. Kadyrov, Ch. Fischer, U. Schmidt, A. Börner, Tetrahedron: Asymmetry 2002, 13, 1615. A New Hydroxydiphosphine as a Ligand for Rh(I)-Catalysed Enantioselective Hydrogenation. |
| 56. | D. Heller, H.-J. Drexler, J. You, K. Drauz, H.-P. Krimmer, A. Börner, Chem. Eur. J. 2002, 8, 5196. On the Enantioselective Hydrogenation of Isomeric Methyl 3-Acetamidobutenoates with Rh(I) Complexes. |
| 55. | A. Börner, Traditio et Innovatio, 2002, 7, 4. Vom Contergan-Skandal zum Nobelpreis für Chemie 2001. |
| 54. | C. Kunze, D. Selent, I. Neda, R. Schmutzler, W. Baumann, A. Börner, Z. Allgem. Anorg. Chem. 2002, 628, 779. Calix[4]arene based bis-phosphonites, bis-phosphites and bis-O-acyl phosphites as ligands in the rhodium(I) catalyzed hydroformylation of 1-octene. |
| 53. | V. Tararov, R. Kadyrov, T. H. Riermeier, A. Börner, Adv. Synth. Catal. 2002, 344, 200. A Scrutiny on the Reductive Amination of Carbonyl Compounds Catalyzed by Homogeneous Rh(I) Diphosphane Complexes. |
| 52. | V. Tararov, R. Kadyrov, Z. Kadyrova, N. Dubrouvina, A. Börner, Tetrahedron: Asymmetry 2002, 13, 25-28. An Improved Synthesis of Enantiopure 2-Azabicyclo[2.2.1]heptane-3-carboxylic Acid. |
| 51. | V. Tararov, R. Kadyrov, T. H. Riermeier, A. Börner, Synthesis 2002, 375-380. Synthesis of N-(dialkylaminoalkyl) alcohols by homogeneously catalysed hydrogenolysis of cyclic N,O-acetals. |
| 50. | C. Kunze, D. Selent, R. Schmutzler, I. Neda, A. Spannenberg, A. Börner, Heteroatom Chem. 2001, 12, 577. Synthesis of new calix[4]arene based phosphorus ligands and their application in Rh(I) catalyzed hydroformylation of 1-octene. |
| 49. | J. Holz, R. Stürmer, U. Schmidt, H.-J. Drexler, D. Heller, H.-P. Krimmer, A. Börner, Eur. J. Org. Chem. 2001, 4615. Synthesis of Chiral 2,5-Oxymethyl Functionalized Bisphospholanes and their Application in the Rh- and Ru-Catalyzed Enantioselective Hydrogenation. |
| 48. | D. Heller, J. Holz, H.-J. Drexler, J. Lang, H.-P. Krimmer, K. Drauz, A. Börner, J. Org. Chem. 2001, 66, 6816. Pressure dependent highly enantioselective hydrogenation of unsaturated β-amino acid precursors. |
| 47. | D. Selent, D. Hess, K.-D. Wiese, D. Röttger, C. Kunze, A. Börner, Angew. Chem. 2001, 113, 1739; Angew. Chem. Int. Ed. 2001, 40, 1696. Rhodiumkatalysierte isomerisierende Hydroformylierung interner Olefine mit einer Klasse neuartiger Phosphorliganden. |
| 46. | I. Komarov, A. Börner, Angew. Chem. 2001, 113, 1237-1239. Angew. Chem. Int. Ed. 2001, 40, 1197-1200. Hochenantioselektiv oder nicht? - Chirale Monophosphorliganden in der asymmetrischen Hydrierung. |
| 45. | A. Börner, D. Heller, Tetrahedron Lett. 2001, 42, 233. The Economic Use of Precious Chiral Diphosphine Ligands - DuPHOS and its Rhodium(I) COD- and NBD-Complexes. |
| 44. | V. Tararov, R. Kadyrov, T. H. Riermeier, A. Börner, Chem. Commun. 2000, 1867. On the reductive amination of aldehydes and ketones catalyzed by homogeneous Rh(I) complexes. |
| 43. | J. Holz, R. Kadyrov, S. Borns, D. Heller, A. Börner, J. Organomet. Chem. 2000, 603, 61. Cooperative Attractive Interactions in Asymmetric Hydrogenations with Dihydroxydiphosphine Rh(I) Catalysts - A Competition Study. |
| 42. | V. Tararov, R. Kadyrov, T. H. Riermeier, J. Holz, A. Börner, Tetrahedron Lett. 2000, 41, 2351. Rhodium(I) Catalyzed Asymmetric Hydrogenation of Enamines. |
| 41. | D. Selent, D. Röttger, K.-D. Wiese, A. Börner, Angew. Chem. 2000, 112, 1694. Neuartige oxyfunktionalisierte Phosphonitliganden für die Hydroformylierung isomerer n-Olefine. |
| 40. | M. Quirmbach, J. Holz, V. I. Tararov, A. Börner, Tetrahedron 2000, 56, 775. Synthesis of Heterofunctionalized Multidentate Diphosphines and their Application in Ru(II)-Catalyzed Asymmetric Transfer Hydrogenation. |
| 39. | V. Tararov, V. S. Larichev, M. A. Moscalenko, L. V. Yashkina, Viktor N. Khrustalev, M. Yu. Antipin, A. Börner, Y. N. Belokon’, Enantiomer 2000, 5, 169. Stereoisomerism in Bridged Octahedral Dimeric Complexes with Tetradentate Ligands. Diastereospecific Formation of syn-DD-(cis-β-L)TiO2 (L = Chiral Salen Type Ligands). |
| 38. | V. Tararov, R. Kadyrov, T. H. Riermeier, J. Holz, A. Börner, Tetrahedron: Asymmetry 1999, 10, 4009. Phosphines versus Phosphinites as Ligands in the Rhodium Catalyzed Asymmetric Hydrogenation of Imines - A Systematic Study. |
| 37. | J. Holz, D. Heller, R. Stürmer, A. Börner, Tetrahedron Lett. 1999, 40, 7059. Synthesis of the First Water-Soluble Chiral Tetrahydroxy Diphosphine Rh(I)-Catalyst for Enantioselective Hydrogenation. |
| 36. | M. Quirmbach, A. Kless, J. Holz, V. Tararov, A. Börner, Tetrahedron: Asymmetry 1999, 10, 1803. Construction of Chiral Ti(IV)-Rh(I)-Salenophos Complexes and their Application in the Asymmetric Hydroformylation of Functionalized Olefins. |
| 35. | M. Bühl, W. Baumann, R. Kadyrov, A. Börner, Helv. Chim. Acta 1999, 82, 811. Variable Coordination Modes Realised with a Hydroxyalkyldiphosphane as a Hemilabile Ligand: A Combined 103Rh NMR and Density-Functional Study. |
| 34. | S. Borns, R. Kadyrov, D. Heller, W. Baumann, J. Holz, A. Börner, Tetrahedron: Asymmetry 1999, 10, 1425. Counter-Ligand and Solvent Dependent Oxygen-Metal Interactions of Hemilabile Coordinating Hydroxy Groups in Chiral Diphosphine Rhodium(I) Hydrogenation Catalysts. |
| 33. | S. Trinkhaus, R. Kadyrov, J. Holz, R. Selke, L. Götze, A. Börner, J. Mol. Catal. A.: Chemical 1999, 144, 15. Internal versus external ionic functionalities - A comparative study in the asymmetric hydrogenation in water as solvent. |
| 32. | R. Kadyrov, A. Börner, R. Selke, Eur. J. Inorg. Chem. 1999, 705. Conformations and Dynamic Behaviour of Rh-Complexes with 1,4-Bis(diphenylphosphanyl)butane, DIOP and its HO-Analogue. |
| 31. | J. Holz, M. Quirmbach, U. Schmidt, D. Heller, R. Stürmer, A. Börner, J. Org. Chem. 1998, 63, 8031. Synthesis of a New Class of Functionalized Chiral Bisphospholane Ligands and the Application in Enantioselective Hydrogenations. |
| 30. | J. J. Almena Perea, A. Börner, P. Knochel, Tetrahedron Lett. 1998, 39, 8073. A Versatile Modular Approach to New Chiral C2-Symmetrical Ferrocenyl Ligands: Highly Enantioselective Rh-Catalyzed Hydrogenation of α-Acetamidoacrylic Acid Derivatives. |
| 29. | S. Borns, R. Kadyrov, D. Heller, W. Baumann, A. Spannenberg, R. Kempe, J. Holz, A. Börner, Eur. J. Inorg. Chem. 1998, 1291. Catalytic and Structural Features of Hydroxy and Methoxy Groups as Hemilabile Coordinating Ligands in Chiral Diphosphane Rhodium(I) Hydrogenation Catalysts. |
| 28. | R. Selke, J. Holz, A. Riepe, A. Börner, Chem. Eur. J. 1998, 5, 769. Impressive enhancement of the enantioselectivity for a hydroxy group carrying Rh(I) bisphosphine catalyst by micelle forming amphiphiles in water. |
| 27. | R. Kempe, A. Spannenberg, C. Lefeber, A. Börner, Z. Kristall. 1998, 213, 217. 1,2-Bis(trimethylsilyl)vinyl-diphenylphosphonylmethoxy]zirconocene. |
| 26. | Kless, J. Holz, H. Reinke, A. Börner, J. Organomet. Chem.1998, 553, 99. Studies on the formation of uniform η3-coordinated triphos-Mo(0)-complexes. |
| 25. | A. Kless, A. Börner, D. Heller, R. Selke, Organometallics 1997, 16, 2096. Ab Initio Studies of Novel Intermediates in Hydrogenation of N-Alkenylamides by Rhodium(I) Complexes. |
| 24. | S. Trinkhaus, J. Holz, R. Selke, A. Börner, Tetrahedron Lett. 1997, 38, 807. A Novel Method for the Synthesis of Chiral Sulfonated Phosphines. |
| 23. | D. Heller, J. Holz, S. Borns, A. Spannenberg, R. Kempe, U. Schmidt, A. Börner, Tetrahedron: Asymmetry 1997, 8, 213. Influence of a Remote Hydroxy Group in the Ligand on the Reactivity of a Chiral Hydrogenation Catalyst. |
| 22. | A. Kless, C. Lefeber, A. Spannenberg, R. Kempe, W. Baumann, J. Holz, A. Börner, Tetrahedron 1996, 52, 14599. The First Chiral Early-Late Heterobimetallic Complex - A Titanium(IV)-Palladium(II) Complex Based on Salenophos. |
| 21. | J. Holz, A. Kless, A. Börner, Synlett 1996, 3, 267. A New Strategy for the Synthesis of Chiral and Prochiral Triphos Ligands. |
| 20. | Kless, J. Holz, D. Heller, R. Kadyrov, R. Selke, Ch. Fischer, A. Börner, Tetrahedron: Asymmetry 1996, 7, 33. Chiral Phosphinephosphites Having Centers of Axial and Central Chirality in Asymmetric Hydroformylations. |
| 19. | A. Börner, J. Holz, A. Kless, D. Heller, GIT Fachz. Lab. 1995, 339, 1146. Synthese von HydroxyDIOP-Liganden und ihre Anwendung in der rhodiumkatalysierten asymmetrischen Hydrierung. |
| 18. | J. Holz, A. Börner, A. Kless, S. Borns, S. Trinkhaus, R. Selke, D. Heller, Tetrahedron: Asymmetry 1995, 6, 1973. Hydroxyalkylphosphines in Asymmetric Hydrogenations. |
| 17. | A. Börner, A. Kless, R. Kempe, D. Heller, J. Holz, W. Baumann, Chem. Ber. 1995, 128, 767. ß-Alkoxy- and ß-Hydroxyalkylphosphanes as Ligands in the Stereoselective Hydrogenation - a Comparison. |
| 16. | A. Kless, R. Kadyrov, A. Börner, J. Holz, H. B. Kagan, Tetrahedron Lett. 1995, 36, 4601. A New Chiral Multidentate Ligand for Asymmetric Catalysis. |
| 15. | A. Börner, A. Kless, J. Holz, W. Baumann, A. Tillack, R. Kadyrov, J. Organomet. Chem. 1995, 490, 213. Zur Komplexierung von enantiomerenreinen cis- und trans-3-Diphenylphosphino-4-hydroxy-tetrahydrofuranen mit [Rh(COD2]BF4. |
| 14. | A. Börner, J. Ward, W. Ruth, J. Holz, A. Kless, D. Heller, H. B. Kagan, Tetrahedron 1994, 50, 10419. Synthesis and catalytic properties of an acyclic analogue of hydroxy norphos. |
| 13. | A. Börner, J. Holz, A. Kless, D. Heller, U. Berens, Tetrahedron Lett. 1994, 35, 6071. Synthesis of an optically active hydroxy diphosphine, a new ligand for asymmetric catalysis. |
| 12. | A. Börner, R. Kadyrov, M. Michalik, D. Heller, J. Organomet. Chem. 1994, 470, 237. Analogues of DIOP. Synthesis, Reactivity, and NMR Behaviour. |
| 11. | A. Börner, J. Ward, K. Kortus, H. B. Kagan, Tetrahedron: Asymmetry 1993, 4, 2219. A Boron Analogue of DIOP: Synthesis and Properties. |
| 10. | A. Börner, J. Holz, J. Ward, H. B. Kagan, J. Org. Chem. 1993, 58, 6814. Concise Synthesis of Enantiomerically Pure cis- and trans-3-Diphenylphosphino-4-hydroxytetrahydrofuran. |
| 9. | A. Börner, J. Holz, H. B. Kagan, Tetrahedron Lett. 1993, 34, 5273. New Chiral Building Blocks and their Application to the Construction of Chiral Aminoalcohols: Enantiomerically Pure cis- and trans-3-Mesyloxy-4-hydroxy Tetrahydrofurans. |
| 8. | J. Ward, A. Börner, H. B. Kagan, Tetrahedron: Asymmetry 1992, 3, 849. Synthesis of 6-endo-hydroxynorphos, a potential ligand for construction of chiral bimetallic catalysts. |
| 7. | A. Börner, H.-W. Krause, Pharmazie 1990, 45, 531. A convenient synthesis of (R)-phenylalaninol. |
| 6. | A. Börner, H.-W. Krause, J. prakt. Chem. 1990, 332, 307. (1S,2S)-2-Amino-1-aryl-propane-1,3-diols as convenient educts for the synthesis of homochiral (S,S)-norpseudoephedrine. |
| 5. | A. Börner, G. Voss, Synthesis 1990, 7, 573. An efficient synthesis of (1S,2S)-1-acetoxyl-1-aryl-3-halo-phthalimidopropanes. |
| 4. | A. Börner, H.-W. Krause, Tetrahedron Lett. 1989, 30, 929. A convenient synthesis of optically pure (S,S)-norpseudoephedrine. |
| 3. | A. Börner, H.-W. Krause, K. Kortus, React. Kinet. Catal. Lett. 1988, 36, 103. Enantioface-differentiating transferhydrogenation of ethyl acetate on modified Raney-nickel. |
| 2. | H. Kristen, I. Meerwald, A. Börner, Pharmazie 1986, 41, 551. Acyclische C-Nucleoside mit 1,2,4-Triazolen im Aglycon. |
1. | A. Börner, H. Kristen, K. Peseke, M. Michalik, J. prakt. Chem. 1986, 328, 21. Darstellung und Charakterisierung von 5(S)- bzw. 5(R)-Tetrahydroxybutyl-3-methyl-1,3-oxazolidinen. |
| 2. | A. Börner, R. Franke, Hydroformylation. Fundamentals, Processes, and Aplications in Organic Synthesis. Volume 1 and 2, Wiley-VCH, Weinheim, (März) 2016. |
1. | Phosphorus Ligands in Asymmetric Catalysis - Synthesis and Application, A. Börner, Hrsg.; Wiley-VCH, Weinheim, 2008, 3 Volumes. |
| 49. | A. Börner, R. Jackstell, Phosphorus Ligands, In Applied Homogeneous Catalysis with Organometallic Compounds, M. Beller, R. Paciello (Hrsg.), Wiley-VCH, Weinheim, 2016, in press. |
| 48. | A. Börner, R. Franke, Hydroformylation, In Applied Homogeneous Catalysis with Organometallic Compounds, M. Beller, R. Paciello (Hrsg.), Wiley-VCH, Weinheim, 2016, in press. |
| 47. | G. Morales Torres, Robin Frauenlob, R. Franke, A. Börner, Catal. Sci. Technol. 2015, 5, 34-54. Production of alcohols via hydroformylation. |
| 46. | M. Vilches-Herrera, L. Domke, A. Börner, ASC Catal. 2014, 4, 1707-1724. Isomerization-Hydroformylation Tandem Reactions. |
| 45. | E. V. Gusevskaya, J. Jiménez-Pinto, A. Börner, ChemCatChem 2014, 6, 382-411. Hydroformylation in the Realm of Scents. |
| 44. | R. Franke, A. Börner, Hydroformylation – State of the Art. In 75 Jahre Oxo-Synthese, Oxea GmbH, 2013. |
| 43. | A. Börner, R. Jackstell, Phosphorus Ligands, In Applied Homogeneous Catalysis with Organometallic Compounds, M. Beller, R. Paciello (Hrsg.), Wiley-VCH, Weinheim, 2013, in press. |
| 42. | A. Börner, R. Franke, A. Christiansen, Hydroformylation, In Applied Homogeneous Catalysis with Organometallic Compounds, M. Beller, R. Paciello (Hrsg.), Wiley-VCH, Weinheim, 2013, in press. |
| 41. | R. Franke, D. Selent, A. Börner, Chem. Rev. 2012, 112, 5675–5732. Applied Hydroformylation. |
| 40. | S. Lühr, J. Holz, A. Börner, ChemCatChem 2011, 3, 1708-1730. Some new developments in the synthesis of chiral phosphorus ligands. |
| 39. | B. Schäffner, F. Schäffner, S. Verevkin, A. Börner, Chem. Rev. 2010, 110, 4551-4581. Organic Carbonates as Solvents in Synthesis and Catalysis. |
| 38. | A. Börner, Selective Hydrogenation, In Catalysis, M. Beller, A. Reinken, R. van Santen (Hrsg.), Wiley-VCH, Weinheim, 2010. |
| 37. | N. V. Dubrovina, I. A. Shuklov, A. Börner, Synthesis of Phosphepines and Application in Asymmetric Catalysis, In Targets in Heterocyclic Systems - Chemistry and Properties, D. Spinelli (Hrsg.), Italian Society of Chemistry, 2009 in press. |
| 36. | B. Schäffner, S. P. Verevkin, A. Börner „Grüne“ Lösungsmittel für Synthese und Katalyse, Organische Carbonate, Chemie in unserer Zeit, 2009, 43, 12-21. |
| 32. | J. Holz, A. Börner, Chiral Polyphosphorous-Ligands, in Phosphorus Ligands in Asymmetric Catalysis, A. Börner, Hrsg.; Wiley-VCH, Weinheim, 2008, 809-827. |
| 29. | V. Andrushko, A. Börner, Chiral Alkoxy Phosphines, in Phosphorus Ligands in Asymmetric Catalysis, A. Börner, Hrsg.; Wiley-VCH, Weinheim, 2008, 715-748. |
| 28. | V. Andrushko, A. Börner, Chiral Hydroxy Phosphines, in Phosphorus Ligands in Asymmetric Catalysis, A. Börner, Hrsg.; Wiley-VCH, Weinheim, 2008, 633-714. |
| 25. | J. Holz, M.-N. Gensow, O. Zayas, A. Börner, Current Organic Chemistry, 2007, 11, 61-106. Synthesis of Chiral Heterocyclic Phosphines for Application in Asymmetric Catalysis. |
| 24. | Redoxreaktionen, in Chemie für Mediziner, Hrsg. C. Diez, C. Benz, A. Börner, A. Simm, S. Vamvakas, Standhartinger; Wissenschaftliche Verlagsgesellschaft Stuttgart, 2005, 92-111. |
| 23. | Säuren und Basen, in Chemie für Mediziner, Hrsg. C. Diez, C. Benz, A. Börner, A. Simm, S. Vamvakas, Standhartinger; Wissenschaftliche Verlagsgesellschaft Stuttgart, 2005, 76-91. |
| 22. | A. Christiansen, A. Börner, Enantioselective Olefine Isomerizations, in Handbook of CH Transformations, Hrsg. G. Dyker, Wiley-VCH, 1. Auflage, 2005, 430-438. |
| 21. | M.-N. Gensow, A. Börner, Other Concepts - Hydroxyphosphines, in Multiphase Homogeneous Catalysis, Hrsg. B. Cornils, W. A. Herrmann, Wiley-VCH, 1. Auflage, 2005, 89-93. |
| 20. | V. I. Tararov, A. Börner, Synlett 2005, 203-211. Account: Approaching Highly Enantioselective Reductive Amination. |
| 17. | A. Börner, J. Holz, Olefin Hydrogenation, in Transition Metals for Fine Chemicals and Organic Synthesis, Hrsg. M. Beller, C. Bolm, VCH-Wiley, Vol. II, 2. Auflage, Weinheim 2004, Vol. 2, S. 3. |
| 16. | A. Börner, Catalysts for an Aqueous Catalysis, in Aqueous-Phase Organometallic Catalysis, Hrsg. B. Cornils, W. A. Herrmann, Wiley-VCH, 2. Auflage, 2003, 187-193. |
| 15. | Stichworte in ABC of Catalysis - A Concise Encyclopedia, Hrsg. B. Cornils, W. A. Herrmann, R. Schlögl, C.-H. Wong, VCH-Wiley, 2. Auflage, Weinheim 2003. |
| 14. | I. V. Komarov, A. Börner, Organic Synthesis Highlights V, Hrsg. H.-G. Schmalz, T. Wirth, Wiley-VCH, 2002, 194. Highly Enantioselective or Not? - Chiral Monodentate Monophosphorus Ligands in the Asymmetric Hydrogenation. |
| 13. | J. Holz, A. Börner, (S,S)-Ethyl-DuPHOS, e-EROS, Encyclopedia of Reagents for Organic Synthesis, Wiley, Chichester, 2001. |
| 12. | A. Börner, Chirality 2001, 13, 625. Biomimetic asymmetric hydrogenation. |
| 11. | A. Börner, Eur. J. Inorg. Chem. 2001, 327. Microreview: The Effect of Internal Hydroxy Groups on the Asymmetric Hydrogenations of Functionalized Olefins with Chiral Diphosphane Rh(I) Catalysts. |
| 10. | A. Börner, Chimia Oggi 2000, 48. Review: Chiral Hydroxy Phosphines as Ligands for Asymmetric Hydrogenation and Versatile Building Blocks for Hybride Ligands. |
| 9. | Stichworte in ABC of Catalysis - A concise Encyclopedia, Hrsg. B. Cornils, W. A. Herrmann, R. Schlögl, C.-H. Wong, VCH-Wiley, 1. Auflage, Weinheim 2000. |
| 8. | J. Holz, M. Quirmbach, L. Götze, A. Börner, Recent Research Developments in Organic Chemistry, Transworld Research Network, Trivandrum, 1998, 2, 685. Review: New Methodologies for the Construction of Chiral Hydroxy Phosphines. |
| 7. | M. Ohff, J. Holz, M. Quirmbach, A. Börner Synthesis 1998, 1391. Review: Borane-Complexes of Trivalent Organophosphorus Compounds - Versatile Precursors for the Synthesis of Chiral Phosphine Ligands for Asymmetric Catalysis. |
| 6. | A. Börner, J. Holz, Olefin Hydrogenation, in Transition Metals for Fine Chemicals and Organic Synthesis, Hrsg. M. Beller, C. Bolm, VCH, 1998, Vol. 2, S. 3. |
| 5. | J. Holz, M. Quirmbach, A. Börner, Synthesis 1997, 983. Review: Strategies for the Synthesis of Chiral Hydroxy Phosphines - A Class of Versatile Ligands and Ligand Precursors for Asymmetric Catalysis. |
| 4. | Abteilung Chemie (C. Benz, C. Diez), Physicum, EXAKT, Hrsg. H. Abdolvahab-Emminger, Georg Thieme Verlag, Stuttgart, 1997, S. 645. |
| 3. | A. Börner, S. Borns, D. Heller, J. Holz, R. Kadyrov, A. Kless, R. Selke Jahrbuch der Max-Planck-Gesellschaft 1996, Vandenhoeck & Ruprecht, Göttingen, 1996, S. 779. Kooperative Effekte in der asymmetrischen Katalyse. |
| 2. | A. Börner, Ch. Fischer, D. Heller, J. Holz, M. Schwarze, R. Selke, G. Oehme, Jahrbuch der Max-Planck-Gesellschaft 1995, Vandenhoeck & Ruprecht, Göttingen, 1995, S. 719. Einfluß achiraler Modifikatoren auf die Enantioselektivität chiraler Katalysatoren. |
1. | A. Börner, J. Holz, A. Kless, D. Heller, Jahrbuch der Max-Planck-Gesellschaft 1994, Vandenhoeck & Ruprecht, Göttingen, 1994, S. 697. Bimetallkatalysatoren. |
| 141. | B. Zhang, C. Kubis, A. Börner, R. Franke; Verfahren zur Hydroformylierung von Olefinen mit einem Cobalt-Präkatalysator und einem Bisphosphin-Liganden; EP 21177383 (02.06.2021) |
| 140. | B. Zhang, C. Kubis, A. Börner, R. Franke; Verfahren zur Hydroformylierung von Olefinen mit einem Cobalt-Präkatalysator; EP 21177380 (02.06.2021) |
| 139. | X.-F. Wu, T. Meyer, H. Geng, A. Börner, R. Franke; Verfahren zur Hydroxymethylierung und Hydroformylierung von Alkenen mittels Kupfer-Ligand-Komplex; EP 21168761 (16.04.2021) |
| 138. | X.-F. Wu, T. Meyer, H. Geng, A. Börner, R. Franke; Verfahren zur Hydroxymethylierung und Hydroformylierung von Alkenen mittels CU-Katalysators; EP 21168759 (16.04.2021) |
| 137. | X.-F. Wu, H. Geng, T. Meyer, A. Börner, R. Franke; Verfahren zur Hydroxymethylierung und Hydroformylierung von Alkenen mittels Kupfer-Katalysators; EP 21168758 (16.04.2021) |
| 136. | A. C. Sale, R. Franke, A. Brächer, D. Fridag, A. Markovic, P. Kucmierczyk, J. Knossalla, D. Selent, A. Börner, K. Romeike; Biphosphitliganden auf Basis von Benzpinakol mit einem offenen Flügelbaustein; EP 21163482 (18.03.2021) |
| 135. | A. C. Sale, R. Franke, A. Brächer, D. Fridag, A. Markovic, P. Kucmierczyk, J. Knossalla, D. Selent, A. Börner, K. Romeike; Biphosphitliganden auf Basis von Benzpinakol; EP 21163474 (18.03.2021) |
| 134. | A. C. Sale, R. Franke, A. Brächer, D. Fridag, A. Markovic, P. Kucmierczyk, J. Knossalla, D. Selent, A. Börner, K. Romeike; Biphosphitliganden auf Basis von Benzpinakol und 1,3-Propandiol; EP 21163483 (18.03.2021) |
| 133. | A. C. Sale, R. Franke, A. Brächer, D. Fridag, A. Markovic, P. Kucmierczyk, J. Knossalla, D. Selent, A. Börner, K. Romeike; Liganden auf Basis von Phosphonit-Phosphiten; EP 21163479 (18.03.2021) |
| 132. | X.-F. Wu, Y. Zhang, A. Börner, R. Franke; Verfahren zur Herstellung von 2-Aminobenzoxazinonen aus 1-Azido-2-iodobenzolen und Aminen; EP 21156724 (12.02.2021) |
| 131. | X.-F. Wu, H. Geng, A. Börner, R. Franke; Verfahren zur Alkoxycarbonylierung von Alkylhalogeniden mittels Kupfer-Katalysators; EP 21156723 ( 12.02.2021) |
| 130. | O. Knopff, P. Dupau, J.-J. Riedhauser, N. Poirier, D. Pena Fuentes, A. Börner, L. Marinoni; Process and Intermediates for preparing 3-(cyclohex-1-en-1yl)propanal derivatives; EP 20193779.4 (01.09.2020) |
| 129. | R. Franke, A. Börner, S. Kloß, D. Selent; 6,6'-([1,1'-Biphenyl]-2,3'-diylbis(oxy))didibenzo[d,f][1,3,2]dioxaphosphepine; EP 20191435 (18.08.2020) |
| 128. | R. Franke, D. Selent, A. Börner, A. C. Sale; Neue Diphosphite auf Basis von cis-Butendiol-1,4; EP 20191440 (18.08.2020) |
| 127. | R. Franke, A. Börner, D. Selent; Phosphazyklische Phosphite aus dem Enol des 1-Hydroxy-2-Acetonaphthons; EP 19205651 (28.10.2019) |
| 126. | R. Franke, A. Börner, D. Selent; Phosphazyklische Phosphite aus dem Enol des Pyridoins und Furoins; EP 19205655 (28.10.2019) |
| 125. | R. Franke, A. Börner, D. Selent; Phosphazyklische Phosphite aus dem Enol des Benzoins; EP 19205650 (28.10.2019) |
| 124. | R. Franke, D. Selent, S. Kloß, A. Börner; Biphenolphosphite; EP 19205648 (28.10.2019) |
| 123. | X.-F. Wu, Y. Yuan, A. Börner, R. Franke; Verfahren zur Herstellung von Acylgermanium-Verbiundungen; EP 19205659 (28.10.2019) |
| 122. | R. Franke, A. Börner, D. Selent, S. Kloß; Benzpinacolphosphite; EP 19205658 (28.10.2019) |
| 121. | B. Zhang, A. Börner, D. Selent, R. Franke; Bisphosphitliganden mit butanoat-zentralbaustein; EP 19205657 (28.10.2019) |
| 120. | X.-F. Wu, J. Xu, A. Börner, R. Franke; Verfahren zur Alkoxycarbonylierung von Diazoniumsalzen unter Verwendung von Bisphosphiten; EP 18177699.8 (14.06.2018) |
| 119. | X.-F. Wu, J. Xu, A. Börner, R. Franke; Verfahren zur Alkoxycarbonylierung von Diazoniumsalzen unter Verwendung von Cyclohexyl-Bisphosphinen; EP 18177689.9 (14.06.2018) |
| 118. | X.-F. Wu, J. Xu, A. Börner, R. Franke; Verfahren zur Alkoxycarbonylierung von Diazoniumsalzen unter Verwendung von Tetraphenyl-Bisphosphinen; EP 18177690.7 (14.06.2018) |
| 117. | X.-F. Wu, J. Xu, A. Börner, R. Franke; Verfahren zur Alkoxycarbonylierung von Diazoniumsalzen unter Verwendung von Triphenyl-Monophosphiten; EP 18177692.3 (14.06.2018) |
| 116. | X.-F. Wu, J. Xu, A. Börner, R. Franke; Verfahren zur Alkoxycarbonylierung von Diazoniumsalzen unter Verwendung von Triphenyl-Monophosphinen; EP 18177688 (14.06.2018) |
| 115. | A. Börner, R. Franke, D. Selent; Four-toothed phosphino phosphites; EP 17193151 (26.09.2017) |
| 114. | B. Zhang, A. Börner, D. Selent, R. Franke; Bisphosphite ligands with central butanoate Building block; EP 17193162 (26.09.2017) |
| 113. | B. Zhang, A. Börner, R. Franke; Bisphosphite Ligands with dioxxaphosphepin Building blocks; EP 17193150 (26.09.2017) |
| 112. | R. Franke, A. Börner, D. Selent; Phosphinites with a tertiary Butyl Group Bound directly to the Phosphor; EP 17183998 (31.07.2017) |
| 111. | A. Börner, R. Franke, D. Selent; Phosphinites with two tertiary Butyl Groups Bound directly to the Phosphor; EP 17183984 (31.07.2017) |
| 110. | X.-F. Wu, Z. Yin, X. Qi, A. Börner, R. Franke; Synthesis of 2-(4-(Trifluoromethyl)-4H-Benzo[D][1,3]oxazin-4-one from 1-(4-trifluoromethylbenzoyl)-1H-Benzotriazole by adding palladiumchloride (PDCL2) and Biphephos (6,6'-[(3,3'-Di-Tert-Butyl-5,5'-Dimethoxy-1,1'-Biphenyl-2,2'-Diyl)BIS(Oxy)]BIS(Dibenzo[D,F][1,3,2]Dioxaphosphepine)) as well as similar processes; EP 17184005 (31.07.2017) |
| 109. | R. Franke, A. Börner, D. Selent; Ligands having an O-P-O Bridge between two anthracentriol Building blocks; EP 17183989 (31.07.2017) |
| 108. | K. Dyballa, R. Franke, D. Fridag, D. Hess, D. Selent, A. Börner; Method for the Hydroformylation of cyclooctadiene using 4-([1,1':3',1''-Terphenyl]-2'-yloxy)-S-Dinaphtho[2,1-D:1',2'-F][1,3,2]Dioxaphosphepine; EP 17165994 (11.04.2017) |
| 107. | K. Dyballa, R. Franke, D. Fridag, D. Hess, D. Selent, A. Börner; Method for the Hydroformylation of cyclooctadiene using 2-(Anthracen-9-yloxy)-4,4,5,5-Tetramethyl-1,3,2-Dioxaphospholane; EP 17165992 (11.04.2017) |
| 106. | St. Behrens, G. Torres Morales, A. Börner, R. Franke, D. Selent: Verfahren zur Hydroformylierung von Pentensäureestern; DE 102017206200 (11.04.2017) |
| 105. | A. Börner, R. Franke, D. Selent; Ligands and Method for Hydroformylation using a 5-Methyl-4,4-Diphenyl-1,3,2-Dioxaphospholane; EP 17165989 (11.04.2017) |
| 104. | K. Dyballa, R. Franke, D. Fridag, D. Hess, D. Selent, A. Börner; Method for the Hydroformylation of cyclooctadiene using a Tetraphosphite; EP 17165998 (11.04.2017) |
| 103. | K. Dyballa, R. Franke, D. Selent, A. Börner; Monophosphite with Methylene-Bridged Diphenol and Diphenylphenyl Remnant; EP 16189144 (16.09.2016) |
| 102. | A. Börner, K. Dyballa, R. Franke, D. Selent; Phosphites with a Dihydroxyterphenyl; EP 16187583 (07.09.2016) |
| 101. | A. Börner, K. Dyballa, R. Franke, D. Selent; Phosphites with a Silyloxyphenol; EP 16187581 (07.09.2016) |
| 100. | A. Börner, K. Dyballa, R. Franke, D. Selent; Phosphites with a Dihydroxyterphenyl with a Tetraphenyl Dioxaphospholane; EP 16187584 (07.09.2016) |
| 99. | K. Dyballa, R. Franke, C. Weilbeer, D. Selent, A. Börner; Verfahren zur Reduktion von Diphenylselenoxid;DE 102016211499 (27.06.2016) |
| 98. | K. Dyballa, R. Franke, C. Weilbeer, D. Selent, A. Börner; Verfahren zur Herstellung heterozyklischer Selena-Phosphite; DE 102016211500 (27.06.2016) |
| 97. | K. Dyballa, R. Franke, C. Weilbeer, D. Selent, A. Börner; Verfahren zur Herstellung heterozyklischer Selena-Phosphite durch Umsetzung von Selenodiaryl; DE 102016211501 (27.06.2016) |
| 96. | J. Holz, A. Börner, K. Rumpel; P-chirale Phosphinenliganden und deren Verwendung zur asymmetrischen Synthese; EP 16174225.9 (13.06.2016) |
| 95. | A. Börner, J. Holz, K. Rumpel; P-chiral phosphine lingands and use thereof for asymmetric Synthesis; EP 16168649.8 (06.05.2016) |
| 94. | K. Dyballa, R. Franke, D. Selent, A. Börner, C. Weilbeer; Komplexe von Diphenylseleniden, deren Verwendung und Katalysatorverfahren; DE 102016205885 (08.04.2016) |
| 93. | K. M. Dyballa, R. Franke, D. Selent, A. Börner, C. Weilbeer, Komplexe von Diphenylselenoxiden, deren Verwendung und Katalyseverfahren, DE 102016205888 (08.04.2016). |
| 92. | K. M. Dyballa, R. Franke, D. Fridag, D. Hess, F. Geilen, D. Selent, A. Börner, Pinakolester von Antracen-9-yloxy substituierten Dioxaphospholanen, DE 102016205883 (08.04.2016). |
| 91. | A. Börner, D. Selent, R. Franke, K. Dyballa; Monophosphite mit methylenverbrücktem Diphenol; EP 16000095 (15.01.2016) |
| 90. | D. Hess, A. Börner, D. Selent, D. Fridag, R. Franke, K. M. Dyballa, F. Geilen, G. Morales Torres, Bidentate Diphosphoramidite mit einer Homopiperazingruppe als Liganden für die Hydroformylierung, EP 15201654 (21.12.2015). |
| 89. | D. Hess, A. Börner, D. Selent, D. Fridag, R. Franke, K. M. Dyballa, F. Geilen, G. Morales Torres, Bidentate Diphosphoramidite mit einer Piperazingruppe als Liganden für die Hydroformylierung, EP 15201638 (21.12.2015). |
| 88. | A. Börner, D. Selent, R. Franke, K. M. Dyballa, C. Weilbeer, Heterozyklische Selena-Phosphite sowie Verfahren zu deren Herstellung, EP 15198153 (07.12.2015). |
| 87. | A. Börner, D. Selent, R. Franke, K. M. Dyballa, C. Weilbeer, Organodiarylselenoxide sowie Verfahren zu deren Herstellung, EP 15198150 (07.12.2015). |
| 86. | A. Börner, D. Selent, R. Franke, K. M. Dyballa, C. Weilbeer, Heterocyclische Selena-Bisphosphite sowie Verfahren zu deren Herstellung, EP 15198148 (07.12.2015). |
| 85. | A. Börner, D. Selent, R. Franke, K. M. Dyballa, C. Weilbeer, Heterocyclische an einer Hydroxyl-Gruppe geschützte Selena-Monophosphite sowie Verfahren zu deren Herstellung, EP 15198145 (07.12.2015). |
| 84. | A. Börner, D. Selent, R. Franke, K. M. Dyballa, C. Weilbeer, Heterocyclische Selena-Phosphite sowie Verfahren zu deren Herstellung, EP 15198143 (07.12.2015). |
| 83. | A. Börner, D. Selent, R. Franke, K. M. Dyballa, C. Weilbeer, Komplexe von Selenodiphenole sowie Verfahren zu deren Herstellung, EP 15196197 (25.11.2015) |
| 82. | A. Börner, D. Selent, R. Franke, K. M. Dyballa, C. Weilbeer, Geschützte Selenodiphenole sowie Verfahren zu deren Herstellung, EP 15196191 (25.11.2015), WO 2017088987. |
| 81. | K. M. Dyballa, R. Franke, D. Fridag, H. Häger, D. Hess, F. Geilen, D. Selent, A. Börner, Monophosphite, die ein Cyclododecanol aufweisen, EP 15186164 (23.09.2015). |
| 80. | K. M. Dyballa, R. Franke, D. Fridag, H. Häger, D. Hess, F. Geilen, D. Selent, A. Börner (Evonik Industries), Monophosphite, die ein teilhydriertes BINOL-Derivat aufweisen, EP 15186166 (23.09.2015) |
| 79. | K. M. Dyballa, R. Franke, D. Selent, A. Börner, Monophosphite mit methylenverbrücktem Diphenol, EP 15186167 (23.09.2015). |
| 78. | K. M. Dyballa, R. Franke, D. Fridag, H. Häger, D. Hess, F. Geilen, D. Selent, A. Börner (Evonik Industries), Monophosphite, die ein BINOL-Derivat aufweisen, EP 15186168 (23.09.2015) |
| 77. | J. Schulze, A. Börner, W. Tietz, I. Shuklov; Verwendung von bimetallischen Katalysatoren in einem Verfahren zur Hydrierung von Amiden von Carbonsäuren aus nachwachsenden Rohstoffen; DE 102015201496.7 (28.01.2015) |
| 76. | K. M. Dyballa, R. Franke, D. Selent, A. Börner (Evonik Industries), Bisphosphite die eine Naphthyl-Phenyl-Einheit als Flügelbaustein und eine 2,3‘-Bisphenol-Einheit als Zentral-Baustein aufweisen, EP 14196191 (04.12.2014). |
| 75. | F. Geilen, K. M. Dyballa, R. Franke, D. Fridag, D. Selent, A. Börner, D. Hess (Evonik Industries), Monophosphite die ein Naphthol aufweisen, EP 14196194 (04.12.2014). |
| 74. | F. Geilen, K. M. Dyballa, R. Franke, D. Fridag, D. Selent, A. Börner, D. Hess(Evonik Industries), Phosphoramidite welche eine Phenyl- Phenyl-Einheit oder eine Phenyl-Naphthyl-Einheit aufweisen, EP 14196196 (04.12.2014). |
| 73. | K. M. Dyballa, R. Franke, D. Fridag, D. Selent, A. Börner, (Evonik Industries), Bisphosphite die einen unsymmetrischen Biphenol-Flügel-Baustein aufweisen, EP 14196187 (04.12.2014). |
| 72. | K. M. Dyballa, R. Franke, D. Fridag, D. Selent, A. Börner, (Evonik Industries), Bisphosphite die eine Naphthyl-Phenyl-Einheit als Flügel-Baustein aufweisen, EP 14196189 (04.12.2014). |
| 71. | K. M. Dyballa, R. Franke, D. Selent, A. Börner, (Evonik Industries), Monophosphite die einen unsymmetrischen Biaryl-Baustein aufweisen, EP 14196197 (04.12.2014). |
| 70. | F. Geilen, K. M. Dyballa, R. Franke, D. Fridag, D. Selent, A. Börner, D. Hess (Evonik Industries), Monophosphite die ein Benzpinakol aufweisen, EP 14196195 (04.12.2014). |
| 69. | F. Geilen, K. M. Dyballa, R. Franke, D. Fridag, D. Selent, A. Börner, D. Hess (Evonik Industries), Monophosphite die ein Anthrol aufweisen, EP 14196192 (04.12.2014). |
| 68. | K. M. Dyballa, R. Franke, D. Selent, A. Börner (Evonik Industries), Monophosphite die ein Menthol aufweisen, EP 14196188 (04.12.2014). |
| 67. | K. M. Dyballa, R. Franke, D. Selent, A. Börner (Evonik Industries), Eintopfsynthese zur Herstellung von Diphosphiten und Triphosphiten, EP 14196183 (04.12.2014). |
| 66. | M. Uhlemann, G. Geilen, K. M. Dyballa, R. Franke, D. Fridag, D. Selent, A. Börner, D. Hess (Evonik Industries), Monophosphite die ein Diphenol aufweisen, EP 14196185 (04.12.2014). |
| 65. | K. M. Dyballa, R. Franke, D. Selent, A. Börner (Evonik Industries), Bisphosphite die eine 2,3‘-Biphenol-Einheit Zentral-Baustein aufweisen, EP 14196179 (04.12.2014). |
| 64. | K. M. Dyballa, R. Franke, D. Fridag, D. Selent, A. Börner (Evonik Industries), Bisphosphite die einen unsymmetrischen Biaryl-Zentral-Baustein aufweisen, EP 14196178 (04.12.2014). |
| 63. | M. Beller, A. Börner, R. Jackstell, X. Fang (Leibniz-Institut für Katalyse), Verfahren zur katalytischen Herstellung von symmetrischen und unsymmetrischen Ketonen, DE 102014201126.4 (22.01.2014). |
| 62. | A. Börner, S. Lühr, M. Vilches, R. Franke, K. Dyballa (Evonik Industries), Isomerisierungsarme Hydroformylierung von ölsäureesterhaltigen Gemischen, EP 13198274 (19.12.2013). |
| 61. | A. Börner, D. Selent, E. Benetskiy, R. Franke, K. Dyballa, D. Fridag (Evonik Industries), Phosphoramiditderivate in der Hydroformylierung von ungesättigten Verbindungen, DE 102013214382 (23.07.2013). |
| 60. | A. Börner, D. Selent, E. Benetskiy, R. Franke, K. Dyballa, D. Fridag (Evonik Industries), Phosphoramiditderivate in der Hydroformylierung von olefinhaltigen Gemischen, DE 102013214378 (23.07.2013). |
| 59. | S. Lühr, A. Börner, D. Selent, E. Benetskiy, R. Franke, K. Dyballa, D. Fridag (Evonik Industries) Phosphoramiditderivate in der Hydroformylierung von ungesättigten Verbindungen, DE 102013214373 (23.07.2013). |
| 58. | A. Börner, D. Selent, R. Franke, K. M. Dyballa, D. Hess, D. Fridag, B. Hamers (Evonik Industries), Neue vierzähnige Phosphorliganden mit Hostanox O3 Leitstruktur, DE 102013208097 (03.05.2013). |
| 57. | J. Holz, A. Börner, (Leibniz-Institut für Katalyse), Verfahren zur Herstellung von Citronellal, DE 10 2013 103 563.9 (10.04.2013); (BASF SE) WO 2014167014. |
| 56. | M. Fritsch, A. Boerner, I. Shuklov, Z. Knez (ThyssenKrupp, Industrial Solutions AG), Process for the preparation and isolation of carboxylic esters, DE 102013225215 (06.12.2013), WO 2015082077. |
| 55. | I. Shuklov, M. Fritsch, A. Börner, J. Schulze (ThyssenKrupp Uhde GmbH), Verfahren zur Herstellung von Dicarbonsäuren, DE 102013000328.8 (11.01.2013), WO 2014108163. |
| 54. | I. Shuklov, W. Tietz, A. Börner (ThyssenKrupp Uhde GmbH), Verfahren zur selektiven chemischen Extraktion von Milchsäure aus Polymerblends, DE 102012023609.3 (04.12.2012), WO 2014086840. |
| 53. | I. Shuklov, A. Börner, K. Kühlein, W. Tietz, J. Schulze (ThyssenKrupp Uhde GmbH), DE 102012001201.2 (24.01.2012); Herstellung von Propan-1,2-diol. |
| 52. | D. Selent, A. Börner, R. Franke, D. Hess, B. Kreidler, A. Chistiansen, D. Fridag, (Evonik Oxeno GmbH), DE 102011085883.0 (08.11.2011); Neue Organophosphorverbindungen auf Basis von Anthracentriol; WO 2013068232. |
| 51. | H. Mena, J. Holz, A. Börner, T. Kutsuna, T. Tsyimoto, N. Fushimi, Method for Producing Aromatic Polyalcohol, (Mitsubishi Gas Chemical Company, Inc), JP 2011-138509 (22.06.2011). |
| 50. | M. Uhlemann, A. Börner, S. Doerfelt, Verfahren zur Herstellung von Aldehyden aus Olefinen (Miltitz Aromatics GmbH), DE 102011107930 (19.07.2011). |
| 49. | I. Shuklov, A. Börner, K. Kühlein, J. Schulze, W. Tietz, Herstellung von optisch reinem Propan-1,2-diol (ThyssenKrupp Uhde GmbH), DE 102011107959 (20.07.2011), WO 2013010618. |
| 48. | M. Becker, R. Franke, W. Büschken, A. Börner, J. Holz, Vorrichtung und Verfahren für die kontinuierliche Umsetzung einer Flüssigkeit mit einem Gas, DE 102008041652 (Oxeno Evonik GmbH) (28.08.2008), WO 20100023018. |
| 47. | B. Schäffner, J. Holz, A. Börner, Efficient and highly enantioselective Rh-catalyzed hydrogenations of unsaturated lactate precursors with chiral bisphospholanes as ligands, (Uhde GmbH, Thyssen-Krupp AG) (30.06.2008), EP 2141145, WO 2010000354 |
| 46. | B. Kreidler, K.-D. Wiese, D. Hess, D. Selent, A. Börner, Verfahren zur Abtrennung von 1-Buten aus C4-haltigen Kohlenwasserstoffströmen durch Hydroformylierung, DE 102008002188.1 (Oxeno Evonik GmbH) (03.06.2008), WO 2009146984. |
| 45. | N. Andrushko, V. Andrushko, G. König, A. Börner, (ratiopharm GmbH) (20.08.2007), EP 20070016279, Process for preparing pyrimidine derivatives, WO 2009024323. |
| 44. | V. Andrushko, N. Andrushko, G. König, A. Börner, (ratiopharm GmbH), EP 20070016872, (28.08.2007), Process for preparing pentanoic diacid derivatives, WO 2009/027081. |
| 43. | D. Selent, D. Fridag, D. Hess, K.-D. Wiese A. Börner, (Degussa AG), DE 102007023514.5 (18.05.2007). Stabile Katalysatorvorstufe von Rh-Komplexkatalysatoren (Evonik Industries), WO 200841853 |
| 42. | V. Tararov, A. Korostylev, A. Börner, G. König, P. Bobal, J. Frantisek, J. Stohandl, K. Denike, N. Jeker, <invention-title load-source="patent-office" mxw-id="PT60956503" lang="EN">Process for preparing c5 intermediates and their use in the preparation of n-substituted pyrrole derivatives, CA 2652412 (15.05.2006), WO 2007131528</invention-title> |
| 41. | D. Selent, B. Kreidler, D. Hess, K.-D. Wiese A. Börner, (Degussa AG), DE 102006058682.4 (13.12.2006). Biphosphitliganden für die übergangsmetallkatalysierte Hydroformylierung; WO 2008071508 |
| 40. | A. Börner, N. Dubrovina, M.-N. Birkholz, B. Breit, J. Rudolph, R. Paciello, C. Jaekel, F. Hettche (BASF AG), EP 06122699.9; Übergangsmetallkatalysierte Additionsreaktionen in halogenierten Lösungsmitteln (20.10.2006); WO 2008046918. |
| 39. | V. Tararov, A. Korostylev, A. Börner, G. König, P. Bobál’, J. Frantisek, J. Stohandl, N. Jeker, K. Denike, (ratiopharm GmbH), EP 06005510.0 (17.03.2006). Process for preparing C7 intermediates and their use in the preparation of N-substituted pyrrole derivatives; WO 2007107276 |
| 38. | J. Holz, A. Börner, T. H. Riermeier, A. Monsees, R. Kadyrov, J. Almena (Degussa AG), DE 102005053079.6 (04.11.2005), Halogenphospholane und deren Herstellung; WO 2007051679 |
| 37. | V. Tararov, G. König, A. Börner, A. Korostylev (ratiopharm GmbH), Verfahren zur Herstellung von Statinen, DE 102005022284.6 (13.05.2005). |
| 36. | V. Tararov, A. Korostylev, A. Börner, G. König, P. Bobál’, J. Frantisek, G. König, N. Jeker, K. Denike, J. Stohandl, (ratiopharm GmbH), EP 2005006577.0 (24.03.2005), Process for preparing C5 intermediates and their use in the preparation of N-substituted pyrrol derivatives |
| 35. | J. Holz, O. Zayas, A. Börner, A. Monsees, T. H. Riermeier, R. Kadyrov, J. Almena (Degussa AG), DE 102005014054.8 (23.03.2005), Elektronenarme Bisphospholanliganden und -Katalysatoren; WO 2006100165 |
| 34. | J. Holz, A. Börner, A. Monsees, J. Almena, T. H. Riermeier, V. Zayas, R. Kadyrov, (Degussa AG), DE 102005014055.6 (23.03.2005), WO 2006/100169. Unsymmetrisch substituierte Phospholankatalysatoren |
| 33. | D. Selent, A. Börner, K. Wiese, D. Ortmann, C. Borgmann, D. Hess, O. Moeller, <invention-title load-source="patent-office" mxw-id="PT15552407" lang="DE">Verfahren zur Hydroformylierung von Olefinen in Anwesenheit von neuen phosphororganischen Verbindungen, DE 102004013514 (19.03.2004), WO 2005090276</invention-title> |
| 32. | A. Börner, J. Holz, T. Riermeier, A. Monsees, J. Almena (Degussa AG), DE 102004051 456.9 (22.10.2004), WO 2006/045388, Neue Bisphospholan-Katalysatoren |
| 31. | P. Bobál’, J. Frantisek, G. König, N. Jeker, K. Denike, V. Tararov, J. Stohandl, A. Börner (ratiopharm GmbH), EP 2004030150 (20.12.2004). Process for preparing pyrrole derivatives and intermediates; WO 2006066823 |
| 30. | A. Börner, J. Holz, T. Riermeier, A. Monsees, B. Gotov, J. Almena, R. Kadyrov, W. Zeiß, I. Nagl, K. Drauz, W. Meichelböck (Degussa AG), DE 10353831.3 (18.11.2003), WO 2005049629. Verfahren zur Herstellung von Bisphospholanliganden |
| 29. | V. Tararov, A. Börner, G. König (Ratiopharm GmbH), DE 10352659.5 (11.11.2003), WO 2005/047276. Verfahren zur Herstellung von Statinen |
| 28. | A. Börner, A. Korostylev, V. Tararov, A. Monsees (Degussa AG), DE 10349399.3 (21.10.2003). Verfahren zur Reduktion von Binaphthylderivaten |
| 27. | D. Selent, W. Baumann, A. Börner (IfOK, Rostock) (17.07.2003), DE 10333143. Gaseinleitungs- und -zirkulationsvorrichtung zur Verfolgung von Reaktionen in flüssiger Phase unter Beteiligung gasförmiger Reaktanden unter Normal- und Hochdruck mittels Kernresonanzspektroskopie (Druck-NMR-Spektroskopie) unter stationären Bedingungen |
| 26. | I. Komarov, A. Börner, A. Monsees, R. Kadyrov (Degussa AG), DE 10223593.7 (27.05.2002) WO 03/099832; Hydroxyphosphine und deren Verwendung in der Katalyse |
| 25. | I. Komarov, A. Börner (IfOK, Rostock) DE 10223442.6 (23.05.2002). Neue optisch reine zyklische P-chirale Phosphine, Verfahren zu ihrer Herstellung und deren Verwendung als Liganden für die asymmetrische Hydrierung |
| 24. | J. Holz, A. Börner, A. Monsees, K. Drauz, T. Riermeier, R. Kadyrov, U. Dingerdissen, C. Schneider (Aventis R&T) DE 10214988.7 (04.04.2002). Bisphosphine als bidentate Liganden; WO 03084971. |
| 23. | D. Selent, A. Börner, C. Borgmann, D. Hess, K.-D. Wiese (Oxeno Degussa Hüls Gruppe) DE 10140086.1 (16.08.2001), Neue Phosphitverbindungen und neue Phosphitmetallkomplexe, WO 03016321 |
| 22. | C. Borgmann, D. Selent, A. Börner, D. Hess, K.-D. Wiese (Oxeno Degussa Hüls Gruppe) DE 10140072.1 (16.08.2001), Neue Bisphosphitverbindungen und deren Metallkomplexe; WO03016322 |
| 21. | C. Borgmann, D. Hess, K.-D. Wiese, D. Selent, A. Börner, R. Schmutzler, I. Neda, C. Kunze (Oxeno Olefinchemie GmbH) DE 10140083.7 (16.08.2001), Neue Phosphitverbindungen und deren Metallkomplexe; WO 03016320 |
| 20. | U. Dingerdissen, T. Riermeier, R. Kadyrov, A. Börner, V. Tararov (Degussa AG) DE 10138140 (09.08.2001), Verfahren zur Herstellung von Aminen durch reduktive Aminierung von Carbonylverbindungen unter Transfer-Hydrierungsbedingungen |
| 19. | H.-P. Krimmer, K. Drauz, J. Lang, A. Börner, D. Heller, J. Holz (Degussa AG) DE 101 00 971.2 (11.01.2001); Verfahren zur Herstellung von enantiomeren-angereicherten ß-Aminosäuren |
| 18. | D. Selent, A. Börner, R. Kadyrov, C. Borgmann, D. Hess, K.-D. Wiese, D. Röttger (Oxeno Olefinchemie), DE 10058383.0 (24.11.2000), Neue Phosphininverbindungen und deren Metallkomplexe |
| 17. | D. Röttger, D. Hess, K.-D. Wiese, C. Borgmann, A. Börner, D. Selent, R. Schmutzler, C. Kunze (Oxeno Degussa Hüls Gruppe) DE 10053272.1 (27.10.2000). (Neue) Biphosphitverbindungen und deren Metallkomplexe |
| 16. | A. Börner, R. Kadyrov, D. Hess, D. Röttger, D. Selent (Oxeno Olefinchemie), DE 10031493.7 (28.06.2000). Neue Biphosphitverbindungen und deren Metallkomplexe |
| 15. | V. Tararov, R. Kadyrov, T. Riermeier, A. Börner, U. Dingerdissen (Aventis R&T), DE 19956414.0 (24.11.1999). Verfahren zur Herstellung von chiralen Aminen durch homogen katalysierte asymmetrische Hydrierung von Enaminen |
| 14. | D. Selent, A. Börner, D. Hess, D. Röttger (Oxeno Olefinchemie GmbH), DE 19954510.3 (12.11.1999). Verfahren zur katalytischen Herstellung von Aldehyden aus Olefinen unter Einsatz von Ligandenmischungen |
| 13. | D. Selent, A. Börner, D. Hess, D. Röttger (Oxeno Olefinchemie GmbH), DE 19954721 (12.11.1999), Verfahren zur Herstellung von Aldehyden aus Olefinen durch Hydroformylierung |
| 12. | T. Riermeier, K.-J. Haack, U. Dingerdissen, A. Börner, V. Tararov, R. Kadyrov, (Aventis R&T) DE 19933611 (17.07.1999). (Degussa AG). Verfahren zur Herstellung von Aminen durch homogen katalysierte reduktive Aminierung von Carbonylverbindungen; WO 6105741 |
| 11. | J. Holz, G. Voß, R. Stürmer, A. Börner, M. Klatt (BASF) DE 19845517, (02.10.1998). Verfahren zur Hydrierung von β-Ketoestern |
| 10. | J. Holz, G. Voß, R. Stürmer, A. Börner, (BASF) DE 19824121, (29.05.1998). Herstellung optisch aktiver Phospholane und ihre Anwendung in der asymmetrischen Katalyse |
| 9. | A. Börner, J. Holz, G. Voß, R. Stürmer, (MPG/BASF) DE 19725796, (18.06.1997). Herstellung optisch aktiver Phospholane, deren Metallkomplexe und Anwendung in der asymmetrischen Synthese |
| 8. | A. Börner, G. Voss, (ISIS-Chemie Zwickau) DD 288149 (02.10.1989). Verfahren zur reduktiven Dehalogenierung von a-Arylhalogenalkanen |
| 7. | A. Börner, G. König (ISIS-Chemie Zwickau) DD 275 669 (20.09.1988). Verfahren zur Herstellung optisch aktiver D- bzw. L-threo-2-Amino-1-aryl-propan-1-ole |
| 6. | A. Börner, H. Foken, F. Flöther, H.-W. Krause, (ISIS-Chemie Zwickau) DD 275 668 (20.09.1988). Verfahren zur Herstellung von optisch reinen D- bzw. L-threo-2-Amino-1-aryl-propan-1-olen |
| 5. | A. Börner, H. W. Krause, F. Kropfgans, K. H. Mann, (ISIS-Chemie Zwickau) DD 275 670 (20.09.1988). Verfahren zur Herstellung von D,L-threo-2-Amino-1(p-aminophenyl)propan-1,3-diolen |
| 4. | A. Börner, H. Foken, F. Flöther, H.-W. Krause, (ISIS-Chemie Zwickau) DD 275 667 (20.09.1988). Verfahren zur Herstellung von D,L-threo-2-Amino-1-aryl-3-halogen-propan-1-olen |
| 3. | A. Börner, H.-W. Krause, F. Kropfgans, K.-H. Mann, (ISIS-Chemie Zwickau) DD 275 675 (20.09.1988). Verfahren zur Herstellung von D- bzw. L-threo-2-Amino-1(p-substituierter bzw. unsubsubstituierter phenyl)-propan-1-olen |
| 2. | A. Börner, H.-W. Krause, DD 248 579 (24.04.1986). Verfahren zur katalytisch-asymmetrischen Transferhydrierung mittels heterogener Katalysatoren |
1. | H. Kristen, I. Meerwald, A. Börner, DD 245 876 (24.01.1984). Verfahren zur Herstellung von Hexonsäureamidderivaten |
| 3. | Asymmetric Catalysis on Industrial Scale, H.-U. Blaser, E. Schmidt (Hrsg.), Wiley-VCH, Weinheim, 2004; reviewed in Nachr. Chem. Techn. 2004. |
| 2. | Catalysis in Asymmetric Synthesis, M. J. Williams (Hrsg.); reviewed in Angew. Chem. 2000. |
1. | Ferrocenes, Homogeneous Catalysis - Organic Synthesis - Material Sciences, A. Togni, T. Hayashi (Hrsg.), VCH-Weinheim, 1995; reviewed in Z. Physik. Chem. 1996, 193, 213. |