Publikationen - Prof. Dr. Armin Börner
Publikationen
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. | H. Kristen, I. Meerwald, A. Börner, Pharmazie 1986, 41, 551. Acyclische C-Nucleoside mit 1,2,4-Triazolen im Aglycon |
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 |
4. | A. Börner, H.-W. Krause, Tetrahedron Lett. 1989, 30, 929. A convenient synthesis of optically pure (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 |
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 |
7. | A. Börner, H.-W. Krause, Pharmazie 1990, 45, 531. A convenient synthesis of (R)-phenylalaninol |
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 |
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 |
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 |
11. | A. Börner, J. Ward, K. Kortus, H. B. Kagan, Tetrahedron: Asymmetry 1993, 4, 2219. A Boron Analogue of DIOP: Synthesis and Properties |
12. | A. Börner, R. Kadyrov, M. Michalik, D. Heller, J. Organomet. Chem. 1994, 470, 237. Analogues of DIOP. Synthesis, Reactivity, and NMR Behaviour |
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. |
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 |
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 |
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 |
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 |
18. | J. Holz, A. Börner, A. Kless, S. Borns, S. Trinkhaus, R. Selke, D. Heller, Tetrahedron: Asymmetry 1995, 6, 1973. Hydroxyalkylphosphines in Asymmetric Hydrogenations |
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 |
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 |
21. | J. Holz, A. Kless, A. Börner, Synlett 1996, 3, 267. A New Strategy for the Synthesis of Chiral and Prochiral Triphos Ligands |
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 |
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 |
24. | S. Trinkhaus, J. Holz, R. Selke, A. Börner, Tetrahedron Lett. 1997, 38, 807. A Novel Method for the Synthesis of Chiral Sulfonated Phosphines |
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 |
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 |
27. | R. Kempe, A. Spannenberg, C. Lefeber, A. Börner, Z. Kristall. 1998, 213, 217. 1,2-Bis(trimethylsilyl)vinyl-diphenylphosphonylmethoxy]zirconocene |
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 |
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 |
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. |
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 |
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. |
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 |
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. |
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. |
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 |
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 |
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 |
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) |
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 |
41. | D. Selent, D. Röttger, K.-D. Wiese, A. Börner, Angew. Chem. 2000, 112, 1694. Neuartige oxyfunktionalisierte Phosphonitliganden für die Hydroformylierung isomerer n-Olefine |
42. | V. Tararov, R. Kadyrov, T. H. Riermeier, J. Holz, A. Börner, Tetrahedron Lett. 2000, 41, 2351. Rhodium(I) Catalyzed Asymmetric Hydrogenation of Enamines |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
55. | A. Börner, Traditio et Innovatio, 2002, 7, 4. Vom Contergan-Skandal zum Nobelpreis für Chemie 2001 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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) |
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 |
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 |
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 |
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 |
71. | J. Holz, A. Börner, A. Spannenberg, C. Pribbenow, D. Heller, H.-J. Drexler, Z. Kristall. NCS 2004, 219, 199-200. |
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. |
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 |
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 |
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 |
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 |
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 |
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. |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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, |
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. |
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 |
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 |
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. |
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 |
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 |
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 |
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 species, |
96. | A. Korostylev, V. Andrushko, N. Andrushko, V. I. Tararov, G. König, A. Börner, Highly Enantioselective Hydrogenation of Ethyl 5,5-Dimethoxy-3-oxopentanoate and its Application for the Synthesis of a Statin Precursor, Eur. J. Org. Chem. 2008, 840-846. |
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 |
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 |
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 |
100. | B. Schäffner, J. Holz, S. P. Verevkin, A. Börner, ChemSusChem 2008, 249-253. Organic Carbonates as Alternative Solvent for Palladium-catalyzed Substitution Reactions |
101. | V. N. Emelyanenko, A. V. Toktonov, S. A. Kozlova, S. P. Verevkin, V. Andrushko, N. Andrushko, A. Börner, Structure-Energy Relationships in Unsaturated Esters of Carboxylic acids. Thermochemical Measurements and Ab Initio Calculations, J. Phys. Chem. A, 2008, 112, 4036-404. |
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. |
103. | S. A. Kozlova, V. N. Emel’yanenko, M. Georgieva, S. P. Verevkin, Y. Chernyak, B. Schäffner, A. Börner, Aliphatic Alkyl Carbonates. Vapour Pressures at Ambient Temperatures, J. Chem. Thermodyn. 2008, 40, 1136-1140. |
104. | R. Kadyrov, J. Holz, B. Schäffner, O. Zayas, J. Almena, A. Börner, Synthesis of Chiral b-Aminophosphonates via Rh-Catalyzed Asymmetric Hydrogenation of b-Amido-vinylphosphonates, Tetrahedron: Asymmetry 2008, 19, 1189-1192. |
105. | S. P. Verevkin, V. N. Emel’yanenko, A. V. Toktonov, Y. Chernyak, B. Schäffner, A. Börner, Cyclic Alkylene Carbonates. Experiment and First Principles Calculations for Prediction of Thermochemical Properties, Fluide Phase Equilibria 2008, 268, 1-6. |
106. | V. Andrushko, N. Andrushko, G. König, A. Börner, Highly enantioselective catalytic hydrogenation of a 5-amino-3,5-dioxopentanoic ester, Tetrahedron Lett. 2008, 49, 4836-4839. |
107. | S. P. Verevkin, V. N. Emel’yanenko, A. V. Toktonov, Y. Chernyak, B. Schäffner, A. Börner, Cyclic Alkylene Carbonates. Experiment and First Principles Calculations for Prediction of Thermochemical Properties, J. Chem. Thermodyn. 2008, 40, 1428-1432. |
108. | N. Andrushko, V. Andrushko, T. Thyrann, G. König, A. Börner, Synthesis of enantiopure (R)-2-(4-methoxy-3-(3-methoxypropoxy)-benzyl)-3-methylbutanoic acid a key intermediate for the preparation of Aliskiren, Tetrahedron Lett. 2008, 49, 5980-5982. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
119. | B. Schäffner, V. Andrushko, J. Bayardon, J. Holz, A. Börner, Chirality 2009 in press. Organic Carbonates as Alternative Solvents for Asymmetric Hydrogenation. |
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. |
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. |
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. |
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. |
124. | 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. | 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. | 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. | I. Karamé, G. Nemra-Baydoun, R. Abdallah, A. Kanj, A. Börner, Synth. Commun. 2010, in press. 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. |
128. | 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. | N. Andrushko, V. Andrushko, Peter Roose, K. Moonen, A. Börner, ChemCatChem 2010 in press, Amination of Aliphatic Alcohols and Diols with an Ir-Pincer Catalyst. |
130. | A. Christiansen, D. Selent, A. Spannenberg, W. Baumann, R. Franke, A. Börner, Organometallics 2010 in press. Reaction of Secondary Phosphine Oxides with Rhodium(I). |
131. | A. Christiansen, Ch. Li, M. Garland, D. Selent, R. Ludwig, R. Franke, A. Börner, ChemCatChem 2010 in press, Secondary Phosphane Oxides (SPOs) as Preligands in the Rhodium Catalyzed Hydroformylation. |
132. | I. Shuklov, H. Jiao, J. Schulze, W. Tietz, K. Kühlein, A. Börner, 2010 submitted (ChemSusChem) Studies on the Epimerisation of Diastereomeric Dilactides. |
Bücher
1. | Phosphorus Ligands in Asymmetric Catalysis - Synthesis and Application, A. Börner, Hrsg.; Wiley-VCH, Weinheim, 2008, 3 Volumes. |
Übersichtsartikel und Buchbeiträge
1. | A. Börner, J. Holz, A. Kless, D. Heller, Jahrbuch der Max-Planck-Gesellschaft 1994, Vandenhoeck & Ruprecht, Göttingen, 1994, S. 697. Bimetallkatalysatoren. |
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. |
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 |
4. | Abteilung Chemie (C. Benz, C. Diez), Physicum, EXAKT, Hrsg. H. Abdolvahab-Emminger, Georg Thieme Verlag, Stuttgart, 1997, S. 645. |
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 |
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. |
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 |
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 |
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. |
10. | A. Börner, Chimia Oggi 2000, 48. Review: Chiral Hydroxy Phosphines as Ligands for Asymmetric Hydrogenation and Versatile Building Blocks for Hybride Ligands |
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 |
12. | A. Börner, Chirality 2001, 13, 625. Biomimetic asymmetric hydrogenation |
13. | J. Holz, A. Börner, (S,S)-Ethyl-DuPHOS, e-EROS, Encyclopedia of Reagents for Organic Synthesis, Wiley, Chichester, 2001. |
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 |
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. |
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. |
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. |
18. | V. I. Tararov, R. Kadyrov, T. H. Riermeier, U. Dingerdissen, A. Börner, Org. Prep. Proc. Int. 2004, 36, 99-120, Homogeneous rhodium(I) catalyzed reductive aminations. |
19. | V. I. Tararov, R. Kadyrov, T. H. Riermeier, A. Börner, PharmaChem 2004, 33-36. Homogeneous Transition Metal Catalyzed Enantioselective Reductive Amination. |
20. | V. I. Tararov, A. Börner, Synlett 2005, 203-211. Account: Approaching Highly Enantioselective Reductive Amination, |
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. |
22. | A. Christiansen, A. Börner, Enantioselective Olefine Isomerizations, in Handbook of CH Transformations, Hrsg. G. Dyker, Wiley-VCH, 1. Auflage, 2005, 430-438. |
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. |
24. | Redoxreaktionen, in Chemie für Mediziner, Hrsg. C. Diez, C. Benz, A. Börner, A. Simm, S. Vamvakas, Standhartinger; Wissenschaftliche Verlagsgesellschaft Stuttgart, 2005, 92-111. |
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 |
26. | N. V. Dubrovina, A. Börner, Catalysts for the Fine Chemical Industry, Vol. 5, J. Whittall, S. M. Roberts, Hrsg., Wiley-VCH, Weinheim, 2007, 89-97. Facile synthesis of chiral 1,3-Bis(diphenylphosphino)-1,3-diphenylpropane by self-breeding catalysis |
27. | I. A. Shuklov, N. V. Dubrovina, A. Börner, Synthesis 2007, 2925-2943. Review: Fluorinated alcohols as solvents, co-solvents and additives in homogeneous catalysis |
28. | V. Andrushko, A. Börner, Chiral Hydroxy Phosphines, in Phosphorus Ligands in Asymmetric Catalysis, A. Börner, Hrsg.; Wiley-VCH, Weinheim, 2008, 633-714. |
29. | V. Andrushko, A. Börner, Chiral Alkoxy Phosphines, in Phosphorus Ligands in Asymmetric Catalysis, A. Börner, Hrsg.; Wiley-VCH, Weinheim, 2008, 715-748. |
30. | B. Schäffner, A. Börner, Chiral Phosphine-Phosphine Oxides, Phosphine-Carboxylic acids and Phosphines Bearing Olefinic Groups, in Phosphorus Ligands in Asymmetric Catalysis, A. Börner, Hrsg.; Wiley-VCH, Weinheim, 2008, 785-608. |
31. | I. Otero, A. Börner, Tropos Phosphorus Ligands and Corresponding Chiral Metal Catalysts, in Phosphorus Ligands in Asymmetric Catalysis, A. Börner, Hrsg.; Wiley-VCH, Weinheim, 2008, 207-344. |
32. | J. Holz, A. Börner, Chiral Polyphosphorous-Ligands, in Phosphorus Ligands in Asymmetric Catalysis, A. Börner, Hrsg.; Wiley-VCH, Weinheim, 2008, 809-827. |
33. | N. Andrushko, A. Börner, Phosphine Boranes and Related Trivalent P-Compounds as Intermediates in the Syntheses of Chiral Ligands and Organocatalysts, in Phosphorus Ligands in Asymmetric Catalysis, A. Börner, Hrsg.; Wiley-VCH, Weinheim, 2008, 1275-1347. |
34. | V. Andrushko, N. Andrushko, A. Börner, Bidentate P-Ligands with Additional Functional Groups – Concepts of Hemilability and Secondary Interactions, in Phosphorus Ligands in Asymmetric Catalysis, A. Börner, Hrsg.; Wiley-VCH, Weinheim, 2008, 886-914. |
35. | A. Börner, M. Beller, B. Wünsch „Hydroaminomethylation of Alkenes“ in Science of Synthesis, Houben-Weyl Methods of Molecular Transformation”, D. Enders, S. Schaumann (Hrsg.), Thieme-Verlag, Stuttgart, 2009, Vol. 40a, 111-117. |
36. | B. Schäffner, S. P. Verevkin, A. Börner „Grüne“ Lösungsmittel für Synthese und Katalyse, Organische Carbonate, Chemie in unserer Zeit, 2009, 43, 12-21. |
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. |
38. | A. Börner, Selective Hydrogenation, In Catalysis, M. Beller, A. Reinken, R. van Santen (Hrsg.), Wiley-VCH, Weinheim, 2010. |
39. | B. Schäffner, F. Schäffner, S. Verevkin, A. Börner, Organic Carbonates as Solvents and Synthesis and Catalysis, Chem. Rev. 2010 in press. |
Patente
1. | H. Kristen, I. Meerwald, A. Börner, DD 245 876 (1984). VzH von Hexonsäureamidderivaten |
2. | A. Börner, H.-W. Krause, DD 248 579 (1986). Vz katalytisch-asymmetrischen Transferhydrierung mittels heterogener Katalysatoren |
3. | A. Börner, H.-W. Krause, F. Kropfgans, K.-H. Mann, (ISIS-Chemie Zwickau) DD 275 675 (1988). VzH von D- bzw. L-threo-2-Amino-1(p-substituierter bzw. unsubsubstituierter phenyl)-propan-1-ole |
4. | A. Börner, H. Foken, F. Flöther, H.-W. Krause, (ISIS-Chemie Zwickau) DD 275 667 (1988). VzH von D,L-threo-2-Amino-1-aryl-3-halogen-propan-1-olen |
5. | A. Börner, H. W. Krause, F. Kropfgans, K. H. Mann, (ISIS-Chemie Zwickau) DD 275 670 (1988). VzH von D,L-threo-2-Amino-1(p-aminophenyl)propan-1,3-diolen |
6. | A. Börner, H. Foken, F. Flöther, H.-W. Krause, (ISIS-Chemie Zwickau) DD 275 668 (1988). VzH von optisch reinen D- bzw. L-threo-2-Amino-1-aryl-propan-1-olen |
7. | A. Börner, G. König (ISIS-Chemie Zwickau) DD 275 669 (1988). VzH optisch aktiver D- bzw. L-threo-2-Amino-1-aryl-propan-1-ole |
8. | A. Börner, G. Voss, (ISIS-Chemie Zwickau) DD 288149 (1989). Vz reduktiven Dehalogenierung von a-Arylhalogenalkanen |
9. | A. Börner, J. Holz, G. Voß, R. Stürmer, (MPG/BASF) DE 19725796 A1, 18.06.1997 (EP, WO). Herstellung optisch aktiver Phospholane, deren Metallkomplexe und Anwendung in der asymmetrischen Synthese |
10. | J. Holz, G. Voß, R. Stürmer, A. Börner, (BASF) DE 19824121 A1, 29.05.1998. Herstellung optisch aktiver Phospholane und ihre Anwendung in der asymmetrischen Katalyse |
11. | J. Holz, G. Voß, R. Stürmer, A. Börner, (BASF) DE 19845517 A1, 02.10.1998 (EP, WO). Vz Hydrierung von β-Ketoestern |
12. | T. Riermeier, K.-J. Haack, U. Dingerdissen, A. Börner, V. Tararov, R. Kadyrov, (Aventis R&T) DE 19966611 (17.7.1999). (Degussa AG) EP 1202952 B1 (25.01.2001); US 6,884,887 B1 (26.04.2005). VzH von Aminen durch homogen katalysierte reduktive Aminierung von Carbonylverbindungen |
13. | D. Selent, A. Börner, D. Hess, D. Röttger (Oxeno Olefinchemie GmbH), DE 19954721 (12.11.1999), EP 1099677 (29.09.2000) etc. Verfahren zur Herstellung von Aldehyden aus Olefinen durch Hydroformylierung |
14. | D. Selent, A. Börner, D. Hess, D. Röttger (Oxeno Olefinchemie GmbH), DE 19954510.3 (12.11.1999), EP 1099678 A1 (29.09.2000). Verfahren zur katalytischen Herstellung von Aldehyden aus Olefinen unter Einsatz von Ligandenmischungen |
15. | V. Tararov, R. Kadyrov, T. Riermeier, A. Börner, U. Dingerdissen (Aventis R&T), DE 19956414.0 (24.11.1999). Herstellung von chiralen Aminen durch homogen katalysierte asymmetrische Hydrierung von Enaminen |
16. | A. Börner, R. Kadyrov, D. Hess, D. Röttger (Oxeno Olefinchemie), DE 10031493.7 (28.06.2000). Hydroformylierungskatalysatoren |
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), EP 0208798 (07.08.2002), WO/US 7009068 (07.03.2006). WO/SG 200400155-8 (28.04.2006). Neue Phosphitverbindungen und deren Metallkomplexe |
18. | D. Selent, A. Börner, R. Kadyrov, C. Borgmann, D. Hess, K.-D. Wiese, D. Röttger (Oxeno Olefinchemie), DE 10058383.0 (24.11.2000), EP 1209164 (15.10.2004), US 6,818,770 (16.11.2004), Neue Phosphininverbindungen und deren Metallkomplexe |
19. | V. Tararov, R. Kadyrov, T. Riermeier, A. Börner, U. Dingerdissen (Aventis R&T) 201dg02.de (2000ART039) (2001). Herstellung von achiralen und chiralen Aminen durch homogen katalysierte Hydrierung von N,O-Acetalen, Halbaminalen und Halbaminalethern |
20. | H.-P. Krimmer, K. Drauz, J. Lang, A. Börner, D. Heller, J. Holz (Degussa AG) DE 101 00 971.2 (11.01.2001), EP 011 290 76.43 (13.10.2004); Verfahren zur Herstellung von enantiomeren-angereicherten ß-Aminosäuren |
21. | U. Dingerdissen, T. Riermeier, R. Kadyrov, A. Börner, V. Tararov (Degussa AG) DE 10138140 (09.08.2001), EP 0208748 (06.08.2002), US 10/484.900. Verfahren zur Herstellung von Aminen durch reduktive Aminierung von Carbonylverbindungen unter Transfer-Hydrierungsbedingungen |
22. | 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), US. Verfahren zur katalytischen Herstellung von Aldehyden aus Olefinen unter Einsatz von Ligandenmischungen |
23. | C. Borgmann, D. Selent, A. Börner, D. Hess, K.-D. Wiese (Oxeno Degussa Hüls Gruppe) DE 10140072.1 (16.08.2001), EP 1201675 (24.10.2004), KR 732352 (20.06.2007). Neue Bisphosphitverbindungen und deren Metallkomplexe |
24. | D. Selent, A. Börner, C. Borgmann, D. Hess, K.-D. Wiese (Oxeno Degussa Hüls Gruppe) DE 10140086.1 (16.08.2001), WO 1586577 (04.10.2006). Neue Phosphitverbindungen und neue Phosphitmetallkomplexe. |
25. | J. Holz, A. Börner, A. Monsees, K. Drauz, K.-P. Krimmer (Aventis R&T) DE 10214988.7 (04.04.2002). Bisphosphine als bidentate Liganden; A. Börner, J. Holz, A. Monsees, T. H. Riermeier, R. Kadyrov, C. A. Schneider, U. Dingerdissen, K.-H. Drauz, (Degussa AG) EP 0302162 (03.03.2003), ZL 03807555.5 (30.05.2007); US 2007/0179301 A1 (02.08.2007). |
26. | 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 in der asymmetrischen Hydrierung |
27. | I. Komarov, A. Börner, A. Monsees, R. Kadyrov (Degussa AG), DE 10223593.7 (27.05.2002) WO 03/099832 (04.12.2003) Hydroxyphosphine und ihre Verwendung in der Katalyse |
28. | D. Selent, W. Baumann, A. Börner (IfOK, Rostock) (17.07.2003). 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 |
29. | A. Börner, A. Korostylev, V. Tararov, A. Monsees (Degussa AG), DE 10353831.3 (21.10.2003). Verfahren zur Reduktion von Binaphthylderivaten |
30. | V. Tararov, A. Börner, G. König (Ratiopharm GmbH), DE 10352659.5 (11.11.2003), WO 2005/047276 (09.11.2004). Verfahren zur Herstellung von Statinen |
31. | 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 2006045388 (06.10.2004). Verfahren zur Herstellung von Bisphospholanliganden |
32. | P. Bobál’, J. Frantisek, G. König, N. Jeker, K. Denike, V. Tararov, A. Korostylev, A. Börner (ratiopharm GmbH), EP 2004030150 (20.12.2004). Process for preparing pyrrole derivatives and intermediates |
33. | A. Börner, J. Holz, T. Riermeier, A. Monsees, J. Almena (Degussa AG), DE 102004051 456.9 (22.10.2004), WO 2006/045388 A1 (22.09.2005), WO 2007/051679 A1 (10.05.2007). Verfahren zur Herstellung von neuen Bisphospholankatalysatoren |
34. | J. Holz, A. Börner, A. Monsees, T. H. Riermeier, (Degussa AG), DE 102005014055.6-43 (23.03.2005), EP 2006060409 (02.03.2006), WO 2006/100169 A2 (28.09.2006). Unsymmetrisch substituierte Phospholankatalysatoren |
35. | J. Holz, O. Zayas, A. Börner, A. Monsees, T. H. Riermeier, (Degussa AG), DE 102005014054.8-43 (23.03.2005), EP 2006060092 (20.02.2006). Elektronenarme Bisphospholanliganden und -katalysatoren |
36. | V. Tararov, A. Korostylev, A. Börner, G. König, P. Bobál’, J. Frantisek, G. König, N. Jeker, K. Denike, (ratiopharm GmbH), , EP 2005006577.0 (24.03.2005), WO/2006/066823 (29.06.2006). Process for preparing C5 intermediates and their use in the preparation of N-substituted pyrrol derivatives |
37. | V. Tararov, G. König, A. Börner (ratiopharm GmbH), Verfahren zur Herstellung von Statinen (II), DE 102005022284.6 (13.05.2005). |
38. | J. Holz, A. Börner, T. H. Riermeier, A. Monsees, (Degussa AG), DE 102005053079.6 (04.11.2005), PCT/EP2006/067050 (04.10.2006). Halogenphospholane und deren Herstellung |
39. | V. Tararov, A. Korostylev, A. Börner, G. König, P. Bobál’, J. Frantisek, G. König, 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 |
40. | D. Selent, A. Börner, B. Kreidler, D. Hess, K.-D. Wiese (Degussa AG), , DE 102006034442.1 (21.06.2006), WO, CN. Phosphitliganden für die übergangsmetallkatalysierte Hydroformylierung |
41. | A. Börner, N. Dubrovina, M.-N. Gensow, B. Breit, J. Rudolph, R. Paciello, C. Jaekel, F. Hettche (BASF AG), Übergangsmetallkatalysierte Additionsreaktionen in halogenierten Lösungsmitteln (20.10.2006). |
42. | D. Selent, B. Kreidler, D. Hess, K.-D. Wiese A. Börner, (Degussa AG), DE 102006058682.4 (13.12.2006). Phosphitliganden für die übergangsmetallkatalysierte Hydroformylierung |
43. | D. Selent, B. Kreidler, D. Hess, K.-D. Wiese A. Börner, (Degussa AG), , DE 102007023514.5 (18.05.2007). Stabile Katalysatorvorstufe von Rh-Komplexkatalysatoren (Evonik Industries) CN, WO |
44. | V. Andrushko, N. Andrushko, G. König, A. Börner, Process for preparing pentanoic diacid derivatives (ratiopharm GmbH) (20.08.2007). |
45. | N. Andrushko, V. Andrushko, G. König, A. Börner, Process for preparing pyrimidine derivatives (ratiopharm GmbH) (20.08.2007). |
46. | D. Selent, I. Otero Martinez, A. Börner, B. Kreidler, K.-D. Wiese, Halogenierte Phosphitverbindungen und deren Metallverbindungen, DE 2008E00033 (Oxeno Evonik AG) (31.01.2008) |
47. | 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). |
48. | B. Schäffner, V. Andrushko, J. Holz, A. Börner, J. Schulze, P. Bausch, Efficient and highly enantioselective Rh-catalyzed hydrogenation of unsaturated lactate precursors with chiral bisphospholanes as ligands, DE (Uhde GmbH, Thyssen-Krupp AG) (30.06.2008) |
49. | M. Becker, R. Franke, W. Büschken, A. Börner, J. Holz, Vorrichtung und Verfahren für die kontinuierliche Umsetzung einer Flüssigkeit mit einem Gas, DE 2008E00280 (Oxeno Evonik GmbH) (26.08.2008). |
Rezensionen
1. | Ferrocenes, Homogeneous Catalysis - Organic Synthesis - Material Sciences, A. Togni, T. Hayashi (Hrsg.), VCH-Weinheim, 1995; reviewed in Z. Physik. Chem. 1996, 193, 213. |
2. | Catalysis in Asymmetric Synthesis, M. J. Williams (Hrsg.); reviewed in Angew. Chem. 2000. |
3. | Asymmetric Catalysis on Industrial Scale, H.-U. Blaser, E. Schmidt (Hrsg.), Wiley-VCH, Weinheim, 2004; reviewed in Nachr. Chem. Techn. 2004. |
