123.Meissner A, Pribbenow C, Drexler H-J, and Heller D. ACTA CRYSTALLOGRAPHICA SECTION C: STRUCTURAL CHEMISTRY, 2014, 70, 941-944. Two precatalysts for application in asymmetric homogeneous hydrogenation.
122.Meissner A, Koenig A, Drexler H-J, Thede R, Baumann W, and Heller D. CHEMISTRY – A EUROPEAN JOURNAL, 2014, 20, 14721-14728. New Pentacoordinated Rhodium Species as Unexpected Products during the In Situ Generation of Dimeric Diphosphine-Rhodium Neutral Catalysts.
121.Meissner A, Drexler H-J, Keller S, Selle C, Ratovelomanana-Vidal V, and Heller D. EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, 2014, 2014, 4836-4842. Synthesis and Characterization of Cationic Synphos-Rhodium Complexes.
120.Meissner A, Alberico E, Drexler H-J, Baumann W, and Heller D. CATALYSIS SCIENCE & TECHNOLOGY, 2014, 4, 3409-3425. Rhodium diphosphine complexes: a case study for catalyst activation and deactivation.
119.Gellrich U, Meißner A, Steffani A, Kaehny M, Drexler H-J, Heller D, Plattner DA, Breit B. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2014, 136, 1097-1104. Mechanistic Investigations of the Rhodium Catalyzed Propargylic CH Activation.
118.Fischer C, Koenig A, Meissner A, Thede R, Selle C, Pribbenow C, and Heller D. EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, 2014, 2014, 5849-5855. Quantitative UV/Vis Spectroscopic Investigations of the In Situ Synthesis of Neutral μ2-Chloro-Bridged Dinuclear (Diphosphine)rhodium Complexes.
117.Kohrt C, Baumann W, Spannenberg A, Drexler HJ, Gridnev ID, Heller D CHEMISTRY – A EUROPEAN JOURNAL 2013, 19, 7443-7451. Formation of Trinuclear Rhodium-Hydride Complexes [{Rh(PP*)H}3-(µ2-H)33-H)][anion]2 – During Asymmetric Hydrogenation?
116.Kohrt C, Wienhoefer G, Pribbenow C, Beller M, Heller D CHEMCATCHEM 2013, 5, 2818-2821. Selective Hydrogenation of Alkynes Catalyzed by Trinuclear Rhodium Hydride Complexes of the Type [{(Rh[PP*]H)32-H)33-H)}(BF4)2].
115.Preetz A, Kohrt C, Meissner A, Wei SP, Drexler HJ, Buschmann H, Heller D CATALYSIS SCIENCE & TECHNOLOGY 2013, 3, 462-468. Halide Bridged Trinuclear Rhodium Complexes and their Inhibiting Influence on Catalysis.
114.Wei S, Pedroni J, Meissner A, Lumbroso A, Drexler HJ, Heller D, Breit B CHEMISTRY – A EUROPEAN JOURNAL 2013, 19, 12067-12076. Development of an Improved Rhodium Catalyst for Z-Selective Anti-Markovnikov Addition of Carboxylic Acids to Terminal Alkynes.
113.D. Selent, D. Heller in Catalysis: From Principles to Applications edited by M. Beller, A. Renken, R. A. van Santen, Wiley-VCH, Weinheim, Germany 2012, 465 - 491. In-situ Techniques for Homogeneous Catalysis.
112.D. Heller in Catalysis: From Principles to Applications edited by M. Beller, A. Renken, R. A. van Santen, Wiley-VCH, Weinheim, Germany 2012, 48 - 66. Kinetics in Homogeneous Catalysis.
111.M. Beller, S. Gladiali, D. Heller in Catalysis: From Principles to Applications edited by M. Beller, A. Renken, R. A. van Santen, Wiley-VCH, Weinheim, Germany 2012, 152 – 170. Homogeneous Catalysis.
110.C. Fischer, R. Thede, H.-J. Drexler, A. König, W. Baumann, D. Heller, Chem. Eur. J. 2012, 18, 11920-11928. Investigations into the formation and stability of cationic rhodium diphosphine η6-arene complexes.
109.M. Sawall, C. Fischer, D. Heller, K. Neymeyr, Journal of Chemometrics 2012, 26, 526-537. Reduction of the rotational ambiguity of curve resolution techniques under partial knowledge of the factors. Complementarity and coupling theorems.
108. C. Kohrt, S. Hansen, H.-J. Drexler, U. Rosenthal, A. Schulz, D. Heller, Inorg. Chem. 2012, 51, 7377–7383. Molecular vibration spectroscopy studies on novel trinuclear rhodium-7-hydride complexes of the general type {[Rh(PP*)X]3(µ2-X)3(µ3-X)}(BF4)2 (X = H, D).
107.C. Fischer, C. Selle, H.-J. Drexler, D. Heller, Zeitschr. Anorg. Allg. Chem. 2012, 638, 907-908. Cationic η6-coordinated BINAP rhodium complexes with benzene and toluene.

106.

C. Fischer, A. König, H.-J. Drexler, D. Heller, Zeitschr. Anorg. Allg. Chem. 2012, 638, 905-906. Formation of stable rhodium η6-arene complexes with aniline derivatives.

105.M. Baseda Krüger, C. Selle, D. Heller, W. Baumann, J. Chem. Eng. Data, 2012, 57, 1737-1744. Determination of gas concentrations in liquids by Nuclear Magnetic Resonance: hydrogen in organic solvents.
104.M. Barsukova-Stuckart, N. V. Izarova, R. Barrett, Z. Wang, J. van Tol, H. W. Kroto, N. S. Dalal, B. Keita, D. Heller, U. Kortz, Chem. Eur. J. 2012, 18, 6167-6171. 3d Metal Ions in Highly Unusual Eight-Coordination: The Phosphate-Capped Dodecapalladate(II) Nanocube.
103.A. Meissner, C. Selle, H.-J. Drexler, D. Heller, Acta Cryst. 2012, E68, m259. (+)-Chlorido[(1,2,3,4-η;κP2’)-2’-diphenylphosphanyl-2-diphenylphosphoryl-1,1’-binaphthyl]-rhodium(I) methanolmonosolvate.
102.

C. Fischer, S. Schulz, H.-J. Drexler, C. Selle, M. Lotz, M. Sawall, K. Neymeyr, D. Heller, ChemCatChem 2012, 4, 81-88. The Influence of Substituents in Diphosphine Ligands on the Hydrogenation Activity and Selectivity of the Corresponding Rhodium Complexes as Exemplified by ButiPhane.

101.T. Beweries, J. Thomas, M. Klahn, A. Schulz, D. Heller, U. Rosenthal, ChemCatChem 2011, 3, 1865–1868. Catalytic and Kinetic Studies of the Dehydrogenation of Dimethyl-amine Borane with an iPr Substituted Titanocene Catalyst.
100.

E. Alberico, W. Baumann, J. G. de Vries, H.-J. Drexler, S. Gladiali, D. Heller, Huub J. W. Henderickx, L. Lefort, Chem. Eur. J. 2011, 17, 12683-12695. Unravelling the reaction path of Rhodium-MonoPhosTM catalyzed olefin hydrogenation.

99.

A. Preetz, C. Fischer, C. Kohrt, H.-J. Drexler, W. Baumann, D. Heller Organometallics 2011, 30, 5155-5159. Cationic Rhodium-BINAP Complexes: Full Characterization of Solvate- and Arene-Bridged Dimeric Species.

98.T. Schmidt, W. Baumann, H.-J. Drexler, D. Heller, J. Organomet. Chem. 2011, 696, 1760-1767. Unusual deactivation in the asymmetric hydrogenation of itaconic acid.
97.

C. Fischer, C. Kohrt, H.-J. Drexler, W. Baumann and D. Heller, Dalton Trans.

2011, 40, 4162-4166. Trinuclear rhodium hydride complexes.
96.S. Schulz, C. Fischer, H.-J. Drexler, D. Heller, Acta Cryst. 2010, E66, m1370.  (+)-{1,2-Bis[(2R,5R)-2,5-diethylphospholan-1-yl]ethane-κ2P,P’}(η4-cycloocta-1,5-diene)-rhodium(I) tetrafluoridoborate.
95.C. Fischer, T. Beweries, A. Preetz, H.-J. Drexler, W. Baumann, S. Peitz, U. Rosenthal, D. Heller, Catalysis Today, 2010, 155, 282-288. Kinetic and mechanistic investigations in homogenious catalysis using operando UV/vis spectroscopy.
94.W. Müller, A. Wöhl, S. Peitz, N. Peulecke, B. R. Aluri, B. H. Müller, D. Heller, U. Rosenthal, M. H. Al-Hazmi, F. M. Mousa, ChemCatChem 2010, 2, 1130-1142. A kinetic model for the selective ethene-trimerization to 1-hexene, using a novel CrCl3(THF)3, Ph2PN(iPr)P(Ph)N(iPr)H, AlEt3 - catalyst system.
93.B. R. Aluri, N. Peulecke, S. Peitz, A. Spannenberg, B. H. Müller, S. Schulz, H.-J. Drexler, D. Heller, M. H. Al-Hazmi, F. M. Mosa, A. Wöhl, W. Müller, U. Rosenthal, Dalton Trans. 2010, 7911-7920. Coordination Chemistry of new selective ethylene trimerization ligand Ph2PN(iPr)P(Ph)NH(R) (R = iPr, Et) and preliminary tests in catalysis.
92.A. Preetz, C. Kohrt, H.-J. Drexler, A. J. Torrens, H. Buschmann, M. Garcia Lopez, D. Heller, Adv. Synth. Catal. 2010, 352, 2073-2080. Asymmetric Ring Opening of oxabicyclic alkenes with cationic rhodium complexes.
91.A. Preetz, H.-J. Drexler, S. Schulz, D. Heller, Tetrahedron Asymm. 2010, 21, 1226-1231. BINAP: rhodium-diolefin complexes in asymmetric hydrogenation.
90.A. Wöhl, W. Müller, S. Peitz, N. Peulecke, B. R. Aluri, B. H. Müller, D. Heller, U. Rosenthal, M. H. Al-Hazmi, F. M. Mosa, Chem. Eur. J. 2010, 16, 7833-7842. Influence of process parameters on the reaction kinetics of the chromium-catalyzed trimerization of ethylene.
89.

S. Schulz, H.-J. Drexler, D. Heller, Acta Cryst. 2010, E66, m721–m722. (+)-{1,2-Bis[(2R,5R)-2,5-dimethylphospholan-1-yl]ethane-κ2P,P’}(η4-cycloocta-1,5-diene)rhodium-(I)tetrafluoridoborate.

88.

A. Preetz, W. Baumann, C. Fischer, H.-J. Drexler, T. Schmidt, R. Thede, D. Heller, Organometallics 2009, 28, 3673-3677; Asymmetric hydrogenation. Dimerization of solvate complexes: Synthesis and characterization of dimeric [Rh(DIPAMP)]22+, a valuable catalyst precursor.

87.

T. Schmidt, H.-J. Drexler, J. Sun, Z. Dai, W. Baumann, A. Preetz, D. Heller, Adv. Synth. Catal. 2009, 351, 750-754; Unusual deactivation in the asymmetric hydrogenation of itaconic acid.

86.

T. Beweries, C. Fischer, S. Peitz, V. V. Burlakov, P. Arndt, W. Baumann, A. Spannenberg, D. Heller, U. Rosenthal, J. Am Chem. Soc. 2009, 131, 4463–4469; Combination of Spectroscopic Methods: In Situ NMR and UV/Vis Measurements To Understand the Formation of Group 4 Metallacyclopentanes from the Corresponding Metallacyclopropenes.

85.A. Wöhl, W. Müller, N. Peulecke, B. H. Müller, S. Peitz, D. Heller, U. Rosenthal, J. Mol. Cat. A: Chemical 2009, 297, 1-8. Reaction kinetics of the ethene tetramerization catalyst system CrCl3(THF)3, Ph2PN(iPr)PPh2 and MAO: The unexpected and unusual formation of odd-numbered 1-olefins.
84.P. Arndt, V. V. Burlakov, C. Fischer, D. Heller, M. Klahn, A. Spannenberg, and U. Rosenthal, Inorg. Chem. Commun. 2008, 11, 1452-1454. Reaction of the titanocene alkyne complex Cp2Ti(η2-Me3SiC2SiMe3) with methanol: Preparation and characterization of a novel trinuclear titanium complex [{Cp2Ti(OMe)}2{Ti(OMe)4}].
83.A. Preetz, W. Baumann, H.-J. Drexler, C. Fischer, J. Sun, A. Spannenberg, O. Zimmer, W. Hell, D. Heller, Chem. Asian. J. 2008, 3, 1979-1982; Trinuclear Rhodium Complexes and Their Relevance for Asymmetric Hydrogenation.
82.T. Schmidt, Z. Dai, H.-J. Drexler, M. Hapke, A. Preetz, D. Heller, Chem. Asian J. 2008, 3, 1170-1180; The Majo/Minor Concept: Dependence of the Selectivity of Homogeneously Catalyzed Reactions on Reactivity Ratio and Concentration Ratio of the Intermediates.
81.T. Schmidt, Z. Dai, H.-J. Drexler, W. Baumann, C. Jäger, D. Pfeifer, D. Heller, Chem. Eur. J. 2008, 14, 4469-4471, Novel contributions to the mechanism of the enantioselective hydrogenation of dimethyl itaconate with rhodium complexes.
80.

A. Preetz, H.-J. Drexler, C. Fischer, Z. Dai, A. Börner, W. Baumann, A. Spannenberg, . Thede, D. Heller, Chem. Eur. J. 2008, 14, 1445 - 1451;  Rhodium complex catalyzed asymmetric hydrogenation - Transfer of pre-catalysts into active species.

79.

R. Jackstell, Z. Dai, T. Schmidt, D. Heller and H.-J. Drexler Z. Kristallogr NCS. 2007, 222, 458-462; Crystal structures of 1-(2-(dicyclohexylphosphinophenyl)pyrol-2-dicyclohexylphosphino-rhodium(I) norborna-2,5-diene tetrafluoroborate tetrahydrofuran hemisolvate, [Rh(C34H51NP2)(C7H8)][BF4] · 0.5C4H8O, and 1-(2-(dicyclohexylphosphinophenyl)-pyrol-2-dicyclohexylphosphino-rhodium(I) (Z,Z)-cycloocta-1,5-diene tetrafluoroborate, [Rh(C34H51NP2)(C8H12)][BF4].

78.

J. Holz, A. Börner, D. Heller, H.-J. Drexler Z. Kristallogr NCS. 2007

, 222, 463-464; Crystal structure of (2,3-bis((2R,5R)-2,5-dimethylphosphonalyl)maleic anhydride)-(η4-norbornadiene)-rhodium(I) tetrafluoroborate, [Rh(C7H8)(C16H24O3P2)][BF4].
77.Z. Dai, D. Heller, A. Preetz, H.-J. Drexler Z. Kristallogr NCS. 2007, 222, 111-113; “Crystal structure of (η4-cycloocta-1,5-dien)-N-(2-(diphenylphosphinooxy)-3-(naphthalen-1-yloxy)propyl)-N-(pentan-3-yl)-1,1-diphenylphosphinamine-rhodium(I) tetrafluoroborate, [Rh(C8H12)(C42H43NO2P2)][BF4]”.
76.Z. Dai, D. Heller, A. Spannenberg, H.-J. Drexler Z. Kristallogr NCS. 2007, 222, 109-110; “Crystal structure of (η4-cycloocta-1,5-dien)-((+)-1,1'-bis((2R,4R)-2,4-diethyl-phosphotano)-ferrocene)-rhodium(I) tetrafluoroborate, [Rh(C8H12)Fe(C12H18FeP)2][BF4]”.

75.

D. Heller, A. H. M. de Vries, J. G. de Vries „Catalyst Inhibition and Deactivation in Homogeneous Hydrogenation”, chapter 44 in Handbook of Homogeneous Hydrogenation ed. by . H. G. deVries and C. Elsevier, 1483-1516, Wiley-VCH, 2007.

74.

H.-J. Drexler, A. Preetz, T. Schmidt, D. Heller „Kinetics of homogeneous hydrogen-nations: measurement and interpretation”, chapter 10 in Handbook of Homogeneous Hydrogenation ed. by . H. G. deVries and C. Elsevier, 257-293, Wiley-VCH, 2007.

73.

H.-J. Drexler, J.-T. Sun, D. Heller, U. Berens, M. Kesselgruber, Z. Kristallogr. NCS 2005, 220, 435-436. „Crystal structure of (η4-norborna-2,5-dien){2,3-bis[(S,S)-2,5-dimethyl-phospholanyl]-benzothiophene}rhodium(I) tetrafluoroborate, [Rh(C7H8)(C20H28P2S)][BF4]“.

72.

T. Schmidt, W. Baumann, H.-J. Drexler, A. Arrieta, D. Heller, H. Buschmann, Organometallics 2005, 24, 3842-3848. „About the crystal structure of [Rh((S,S)-DIPAMP)((Z)-2-benzoylamino-3-(3,4-dimethoxyphenyl)-methyl acrylate)]BF4 – Major or minor catalyst-substrate complex?“

71.

H.-J. Drexler, W. Baumann, T. Schmidt, S. Zhang, A. Sun, A. Spannenberg, C. Fischer, H. Buschmann, D. Heller, Angew. Chem. 2005, 117, 1208-1212. „Werden ß-Acylaminoacrylate in gleicher Weise wie α-Acylaminoacrylate hydriert?“. Angew. Chem. Int. Ed. 2005, 44, 1184-1188. „Are ß-Acylaminoacrylates Hydrogenated in the Same Way as α-acylaminoacrylates?“.

70.

W. Braun, B. Calmuschi, H.-J. Drexler,. U. Englert, Detlef Heller, A. Salzer, Acta Cryst. 2004, C60, m532-m536; (R,R)-[1-(1-Diphenylphosphanylethyl)-2-(diphenylphosphanyl)-η6-benzene]-tric-arbonyl-chromium, {(R,R)-[1-(1-Diphenylphosphanylethyl)-2-(diphenyl-phos-phanyl)-η6-benzene]-tricarbonyl-chromium-P,P`-(η4 -norbornadiene)-rhodium tetrafluoro-borate and {(R,R)-[1-(1-Di-phenylphosphanylethyl)-2-(diphenylphosphanyl)- η6-benzene]-tricarbonyl-chromium-P,P`}-(η4 -Z,Z-cycloocta-1,5-diene)-rhodium hexafluorophosphate“.

69.

H.-J. Drexler, S. Zhang, A. Sun, A. Spannenberg, A. Arietta, A. Preetz, D. Heller, Tetrahedron Asymmetry 2004, 15, 2139-2150; (report number 68) Cationic Rh-bisphosphane-diolefin complexes as precatalysts for enantioselective catalysis - what informations do single crystal structures contain regarding product chirality?“.

68.

R. Kempe, A. Spannenberg, D. Heller, H.-J. Drexler, Z. Kristallogr. 2004, 219, 201-202. „Crystal structure of (η4-cycloocta-1,5-dien)(1,2-bis(diethylphosphino)ethane)rhodium(I) tetrafluoroborate, [(C8H12)(C10H24P2)Rh](BF4)“.

67.

J. Holz, A. Börner, A. Spannenberg, C. Pribbenow, D. Heller and H.-J. Drexler, Z. Kristallogr. 2004, 219, 199-200. „Crystal structure of (η4-norborna-2,5-dien)-(1,2-bis((R,R)-2,5-bis-(methoxymethyl)phospholanyl)benzene)rhodium(I) tetrafluoroborate, [(C7H8)(C22H36O4P2)Rh](BF4)“.

66.

H.-J. Drexler, J. You, S. Zhang, C. Fischer, W. Baumann,.A. Spannenberg, D. Heller, Org. Process Res. Dev. 2003, 7, 355-361. „Chiral ß-Amino Acid Derivatives via Asymmetric Hydrogenation”.

65.

W. Braun, A. Salzer, H.-J. Drexler, A. Spannenberg, D. Heller, Dalton Trans. 2003, 1606-1613. „Investigations into the Hydrogenation of Diolefins and Prochiral Olefins Employing the "Daniphos"-Type Ligands”.

64.

J. You, H.-J. Drexler, S. Zhang, C. Fischer, D. Heller, Angew. Chem. 2003, 115, 942-945. „Herstellung und asymmetrische Hydrierung ß-arylsubstituierter ß-Acylaminoacrylate“. Angew. Chem. Int. Ed. 2003, 42, 913-916. „Preparation and asymmetric hydrogenation of ß-aryl-substituted ß-acylamino-acrylates“.

63.

D. Heller, J. Holz, I. Komarov, H.-J. Drexler, J. You, K. Drauz, A. Börner, Tetrahedron : Asymmetry 2002, 13, 2735-2741. “On the enantioselective hydrogenation of isomeric ß-acylamido ß-alkylacrylates with chiral Rh(I) complexes – comparison of phosphine ligands and substrates”.

62.

D. Heller, H.-J. Drexler, J. You, W. Baumann, K. Drauz, H.-P. Krimmer, A. Börner, Chemistry – A European Jornal 2002, 8, 5196-5202. „On the Enantioselective Hydrogenation of Isomeric Methyl 3-Acetamidobutenoates with RhI Complexes”.

61.

D. Heller, H.-J. Drexler, A. Spannenberg, B. Heller, J. You, W. Baumann, Angew. Chem. 2002, 114, 814-817. „Zum inhibierenden Einfluss aromatischer Lösungsmittel auf die Katalysatoraktivität bei asymmetrischen Hydrierungen“. Angew. Chem. Int. Ed. 2002, 41, 777-780. “The inhibiting influence of aromatic solvents on the activity of asymmetric hydrogenations”.

60.

J. Holz, R. Stürmer, U. Schmidt, H.-J. Drexler, D. Heller, H.-P. Krimmer, A. Börner, Eur. J. Org. Chem. 2001, 4615-4624. „Synthesis of Chiral 2,5-Bis(oxymethyl)-Functionalized Bis(phospholane) and Their Applications in Rh- and Ru-Catalyzed Enantioselective Hydrogenations“.

59.

D. Heller, J. Holz, H.-J. Drexler, J. Lang, K. Drauz, H.-P. Krimmer, A. Börner, J. Org. Chem. 2001, 66, 6816-6817. ”Pressure dependent highly enantioselective hydro-genation of unsaturated β-amino acid precursors”.

58.

H.-J. Drexler, W. Baumann, A. Spannenberg, C. Fischer, D. Heller, J. Organomet. Chem. 2001, 621, 89-102. „COD- versus NBD-precatalysts. Dramatic difference in the asymmetric hydrogenation of prochiral olefins with five membered diphosphine Rh-hydrogenation catalysts”.

57.

A. Börner, D. Heller, Tetrahedron Letters 2001, 42, 223-225. “The Economic Use of Precious Chiral Diphosphine Ligands - DuPHOS and its Rhodium(I) COD- and NBD-Complexes“.

56.

H.-J. Drexler, A. Spannenberg, D. Heller, Z. Kristallogr. 2001, 216, 169-171.Crystal structures of (S)-2,3-O,N-bis(diphenylphosphino)-1-(naphthoxy)-2-hydroxy-3-cyclohexylaminopropane rhodium(I)-(Z,Z)-cycloocta-1,5-diene tetrafluoroborate, C51H54BF4NO2P2Rh“.

55.

R. Kempe, A. Spannenberg, D. Heller, H.-J. Drexler, Z. Kristallogr. 2001, 216, 165-168.“Crystal structures of 1,2-bis(dicyclohexylphosphino)-ethane rhodium(I)-norborna-2,5-diene tetrafluoroborate (C33H56BF4P2Rh) and 1,2-bis(dicyclohexylphosphino)-ethane rhodium(I)-(Z,Z)-cycloocta-1,5-diene tetrafluoroborate (C34H60BF4P2Rhx1/2CH3OH)”.

54.

R. Kempe, A. Spannenberg, D. Heller, Z. Kristallogr. 2001, 216, 161-164. “Crystal structures of 1,4-bis(dicyclohexylphosphino)-butane rhodium(I)-norborna-2,5-diene tetrafluoroborate (C35H60BF4P2Rh) and 1,4-bis(dicyclohexylphosphino)-butane rhodium(I)-(Z,Z)-cycloocta-1,5-diene tetrafluoroborate (C36H64BF4P2Rh)”.

53.

R. Kempe, A. Spannenberg, D. Heller, R. Kadirov, V. Fehring, Z. Kristallogr. 2001, 216, 157-160. „Crystal structures of 1,2-bis(diphenylphosphinoxy)-ethane rhodium(I)-norborna-2,5-diene tetrafluoroborate (C33H32BF402P2Rh) and 1,2-bis(diphenylphosphinoxy)-ethane rhodium(I)-(Z,Z)-cycloocta-1,5-diene tetrafluoroborate (C34H36BF402P2RhxC4H8O)”.

52.

R. Kempe, A. Spannenberg, D. Heller, Z. Kristallogr. 2001, 216, 153-156. “Crystal structures of 1,3-bis(diphenylphosphino)-propane rhodium(I)-norborna-2,5-diene tetrafluoroborate (C34H34BF4P2Rh) and 1,3-bis(diphenylphosphino)-propane rhodium(I)-(Z,Z)-cycloocta-1,5-diene tetrafluoroborate (C35H38BF4P2Rh)“.

51.

B. Heller, D. Heller, H. Klein, C. Richter, C. Fischer, G. Oehme, J. Inf. Recording 2000, 25,15-23. „Progress in the photocatalysed Syntheses of Pyridines“.

50.

H. Buschmann, R. Thede, D. Heller, Angew.Chem. 2000, 112, 4197-4200. „Neues zum Ursprung der Homochiralität biologisch relevanter Moleküle“. Angew.Chem. Int. Ed. 2000, 39, 4033-4036. „New developements in the origins of the homochirality of biologically relevant molecules“.

49.

J. Holz, R. Kadyrov, S. Borns, D. Heller, A. Börner, J. Organomet. Chem. 2000, 603, 61-68. „Cooperative Attractive Interactions in Asymmetric Hydrogenations with Dihydroxydiphosphine Rh(I) Catalysts - A Competition Study“.

48.

D. Heller, H.-J. Drexler, C. Fischer, H. Buschmann, W. Baumann, B. Heller, Angew.Chem. 2000, 112, 505-509.„Wie lange kennen wir schon nichtlineare Effekte in der Katalyse?“ Angew.Chem. Int. Ed. 2000, 39, 495-499. „How long have non-linear effects been known in the field of catalysis?“

47.

D. Heller, Stichworte in „Catalysis from A to Z“, eds. B. Cornils, W. A. Herrmann, R. Schlögl, C.-H. Wong, Wiley-VCH, 2000.

46.

J. Holz, D. Heller, R. Stürmer, A. Börner, Tetrahedron Letters 1999, 40, 7059-7062. „Synthesis of the first water-soluble chiral tetrahydroxy diphosphine Rh(I) catalyst for enantioselective hydrogenation“.

45.

S. Borns, R. Kadyrov, D. Heller, W. Baumann, J. Holz, A. Börner, Tetrahedron: Asymmetry 1999, 10, 1425-1431. „Counter-ligand and solvent dependent oxygen-metal interactions of hemilabile coordinating hydroxy groups in chiral diphosphine rhodium(I) hydrogenation catalyst“.

44.

D. Heller, H. Buschmann, H. Neumann, J. Chem. Soc., Perkin Trans. 2 1999, 175-181. „Conditions for maxima and minima as inversion points in the temperature dependence of selection processes“.

43.

H. Neumann, D. Heller, GIT Fachz. Lab. 1998, 11, 1168-1174. „UV/Vis-Spektroskopie mit einer Tauchoptrode - Vorteile und Möglichkeiten“.

42.

B. Heller, D. Heller, P. Wagler, G. Oehme, J. Mol. Catal. A: Chemical 1998, 136, 219-233. „Control of Selectivity in the Cobalt(I) Complex-Catalysed Cocyclisation of Alkynes with Nitriles“.

41.

B. Heller, D. Heller, P. Wagler, C. Fischer, C. Richter, G. Oehme, J. Inf. Recording 1998, 24, 3-8. „Control of selectivity in the photocatalysed synthesis of pyridines“.

40.

J. Holz, M. Quirmbach, U. Schmidt, D. Heller, R. Stürmer, A. Börner, J. Org. Chem. 1998, 63, 8031-8034. „Synthesis of a new class of functionalized chiral bisphospholane ligands and the application in enantioselective hydrogenations“.

39.

S. Borns, R. Kadyrov, D. Heller, W. Baumann, A. Spannenberg, R. Kempe, J. Holz, A. Börner, Eur. J. Inorg. Chem. 1998, 1291-1295. „Catalytic and Structural Features of Hydroxy and Methoxy Groups as Hemilabile Coordinating Ligands in Chiral Diphosphane Rh(I) Hydrogenation Catalysts“.

38.

R. Kempe, A. Spannenberg, D. Heller, Z. Kristallogr. 1998, 213, 636-638. „Crystal structure of (S)-2,3-O,N-bis(diphenylphosphino)-1-(naphthoxy)-2-hydroxy-3-cyclohexylaminopropane rhodium(I)-norborna-2,5-diene tetrafluoroborate, C50H50BF4­NO2P2Rh“.

37.

R. Kempe, A. Spannenberg, D. Heller, Z. Kristallogr. 1998, 213, 633-635. „Crystal structure of (2R,3R,5R,6R)-5,6-bis((diphenylphosphanyl)methyl)-2,3-diethoxy-2,3-dimethyl[1,4]dioxane rhodium(I)-(Z,Z)-cycloocta-1,5-diene tetrafluoroborate, C88H108B2F8O8P4Rh2“.

36.

R. Kempe, A. Spannenberg, D. Heller, Z. Kristallogr. 1998, 213, 631-632. „Crystal structure of phenyl 2,3-bis(O-diphenylphosphino)-ß-D-glyco-pyranoside rhodium(I)-norborna-2,5-diene tetrafluoroborate, C43H42BF4O6P2Rh“.

35.

D. Heller, H. Buschmann, Topics of Catalysis 1998, 5, 159-176. „Selectivity from a kinetic point of view: nonlinear behavior of logarithmic product ratios as a function of the reciprokal temperature“.

34.

B. Heller, D. Heller, G. Oehme, European Photochemistry Accociation: Newsletter 1998, 62, 37-50. „The Light Promoted Co (I) Catalysed Synthesis of Substituted Pyridines“.

33.

R. Kadyrov, D. Heller, R. Selke, Tetrahedron: Asymmetry 1998, 9, 329-340. „New carbohydrate bisphosphites as chiral ligands“.

32.

D. Heller, H. Buschmann, H. Neumann, J. Mol. Catal. A: Chemical 1997, 125, 9-13. „Splitting of the nonlinear temperature dependence of selection processes into the temperature dependencies of single reaction pathways“.

31.

R. Kadyrov, J. Heinicke, M. K. Kindermann, D. Heller, C. Fischer, R. Selke, Chem. Ber. / Racueil 1997, 130, 1663-1670. „P/O ligand systems: Facile synthesis, structure, and catalytic tests of 2’-phosphanyl-1,1’-biphenyl-2-ols and 2’-phosphanyl-1,1’-binaphthyl-2-ols“.

30.

W. Baumann, S. Mansel, D. Heller, S. Borns, Mag. Res. Chem. 1997, 35, 701-706. „Gas bubbles in the NMR tube: an easy way to investigate reactions with gases in liquid phase“.

29.

S. Mansel, D. Thomas, C. Lefeber, D. Heller, R. Kempe, W. Baumann, U. Rosenthal, Organometallics 1997, 16, 2886-2890. „Stable rac-[1,2-Ethylene-1,1’-bis(hapto5-tetrahydroindenyl)] zirconacyclopent-anes - Syntheses, X-ray Crystal Structures, Stability and Catalysis of Ethylene Polyme­rization“.

28.

A. Kless, A. Börner, D. Heller, R. Selke, Organometallics 1997, 16, 2096-2100. „Ab initio studies of rhodium(I)-N-alkenylamide complexes with cis- and trans-coordinating phosphines: relevance for the mechanism of catalytic asymmetric hydrogenation of prochiral dehydroamino acids“.

27.

D. Heller, R. Thede, D. Haberland, J. Mol. Catal. A: Chemical 1997, 115, 273-281. „Kinetic models for catalytic selection processes as applied to asymmetric hydrogenation“.

26.

D. Heller, J. Holz, S. Borns, A. Spannenberg, R. Kempe, U. Schmidt, A. Börner, Tetrahedron: Asymmetry 1997, 8, 213-222. „Influence of a remote hydroxy group in the ligand on the reactivity of a chiral hydrogenation catalyst“.

25.

D. Heller, R. Kadyrov, M. Michalik, T. Freier, U. Schmidt, H.-W. Krause, Tetrahedron: Asymmetry 1996, 7, 3025-3035. „Asymmetric Hydrogenation of Dimethyl Itaconate Catalysed by Rhodium Chelates of Aminophosphine Phosphinites: A Kinetic and NMR Spectroscopical Study“.

24.

B. Heller, D. Heller, G. Oehme, J. Mol. Catal. A: Chemical 1996, 110, 211-219. „Systematic Investigations of the photocatalytic alkyne-nitrile heterotrimerisation to pyridine“.

23.

D. Heller, H. Buschmann, H.-D. Scharf, Angew.Chem. 1996, 108, 1964-1967. „Nichtlineares Temperaturverhalten von Produktverhältnissen bei Selektionsprozessen“. Angew. Chem. Int. Ed. Egl. 1996, 35, 1852-1854. „Nonlinear Temperature Behaviour of Product Ratios in Selektion Processes“.

22.

A. Kless, J. Holz, D. Heller, R. Kadyrov, R. Selke, C. Fischer, A. Börner, Tetrahedron : Asymmetry 1996, 7, 33-36.        „Chiral phosphinephosphites having axial and central chirality in asymmetric hydroformylations“.

21.

D. Heller, S. Borns, W. Baumann, R. Selke, Chem. Ber. 1996, 129 , 85-89. „Kinetic investigations of the hydrogenation of diolefin ligands in catalyst precursors for the asymmetric reduction of prochiral olefins, II“.

20.

A. Börner, J. Holz, A. Kless, D. Heller, GIT Fachz. Lab. 1995, 1146-1147. „Synthese von Hydroxy-DIOP-Liganden und ihre Anwendung in der rhodiumkatalysierten asymmetrischen Hydrierung“.

19.

R. Kadyrov, T. Freier, D. Heller, M. Michalik, R. Selke, J. Chem. Soc., Chem. Commun. 1995, 1745-1746. „Catalyst-substrate complexes of chiral seven-membered ring chelates of rhodium(I)-bis(phosphinites)“.

18.

J. Holz, A. Börner, A. Kless, S. Borns, S. Trinkhaus, R. Selke, D. Heller, Tetrahedron: Asymmetry 1995, 6, 1973-1988. „Hydroxyalkylphosphines in asymmetric hydrogenations“.

17.

A. Börner, A. Kless, R. Kempe, D. Heller, J. Holz, W. Baumann, Chem. Ber. 1995, 128, 767-773. „ß-alkoxy- and ß-hydroxyalkylphosphanes as ligands in the stereoselektive hydrogenation - a comparison“.

16.

D. Heller, K. Kortus, R. Selke, Liebigs Ann. 1995, 575-581. „Kinetische Untersuchungen zur Ligandenhydrierung in Katalysatorvorstufen für die asymmetrische Reduktion prochiraler Olefine“.

15.

A. Börner, J. Ward, W. Ruth, J. Holz, A. Kless, D. Heller, H. Kagan, Tetrahedron 1994, 50, 10419-10430. „Synthesis and catalytic properties of an acyclic analogue of hydroxy norphos“.

14.

B. Heller, P. Wagler, G. Oehme, D. Heller, J. Inf. Rec. Mats. 1994, 21, 685-686. „Systematische Untersuchungen zur photokatalysierten Pyridinsynthese“.

13.

A. Börner, J. Holz, A. Kless, D. Heller, U. Berens, Tetrahedron Letters 1994, 35, 6071-6074. „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, 237-242. „Analogues of DIOP. Synthesis, reactivity, and NMR behaviour“.

11.

G. Oehme, W. Schulz, B. Heller, D. Heller, J. Reihsig, in Catalysis in Environmental and Petrochemical Technologies POSTECH; Pohang South-Korea, 1994 S. 211-228.„The photoassisted synthesis of 2-substituted pyridines by cocyclisation of acetylene and nitriles in presence of catalytic ammounts of cobalt (I)-complexes“.

10.

F. Storz, D. Heller, K. Madeja, J. Mol. Catal. 1993, 84, 33-38. „Ziegler systems as hydrogenation catalysts. Part 2. Dependence of the hydrogenation activity of CoBr2/ Li[AlHn(O-R)4-n] systems from the concentration of the reducing agent“.

9.

B. Schuldt, D. Heller, F. Storz, K. Madeja, J. Mol. Catal. 1993, 81, 195-206. „Ziegler systems as hydrogenation catalysts. Part 1. CoBr2/ Li[AlH(O-t-butyl)3]3 system as a catalyst for the hydrogenation of anthracene“.

8.

R. Selke, C. Facklam, H. Foken, D. Heller, Tetrahedron: Asymmetry 1993, 4, 369-382. „Application of the term "Relative Enantioselectivity" as useful measure for comparison of chiral catalysts, demonstrated on asymmetric hydrogenation of amino acid precursors“.

7.

G. Oehme, B. Heller, W. Schulz, D. Heller, in Solares Testzentrum Almeria“ ed. M. Becker, M Böhmer, K.-H. Funken, Verlag C. F. Müller Karlruhe, 1993, 277-286. (ISBN: 3-7880-7481-7). „Die photoassistierte, durch Cobalt (I)-Komplexe katalysierte Synthese von Pyridinen“.

6.

D. Heller, D. Bilda, H. Fuhrmann, Macromol. Chem. 1992, 193, 2007-2013. „Studies on the polymerization of ethylene using a high-yield MgCl2-supported titanium catalyst, 2“.

5.

D. Heller, Chem. Ing. Tech. 1992, 64, 725-726. „Effektive Methode zur Verfolgung von Polymerisationen gasförmiger Monomerer“.

4.

B. Heller, W. Schulz, G. Oehme, D. Heller, in „Solar Thermal Energy Utilization“ ed. M. Becker, K.-H. Funken, G. Schneider, Springer Verlag Berlin Heidelberg New York, 1992, 91-112. (ISBN: 0-387-55666-4). „The photoassisted (solar-driven) synthesis of 2-substituted pyridines by cocyclisation of acetylene and nitriles inpresence of catalytic ammounts of cobalt (I)-complexes“.

3.

D. Heller, D. Bilda, Chem. Ing. Tech. 1990, 62, 928-930. „Ethen-Löslichkeit in ausgewählten Kohlenwasserstoffen“.

2.

S. Heller, D. Heller, J. Chem. Educ. 1988, 65, 12-15. „A philatelistic history of the discovery and isolation of elements“.

1.

K. Madeja, W.-H. Böhmer, D. Heller, Wiss. Zeitschr. E.-M.-A.- Universität Greifswald, Mathematisch-Naturwissenschaftliche Reihe 1986, 35, 29-34. „Eine rationelle Methode zur Verfolgung gasverbrauchender Reaktionen (II)“.

13.H.-J. Drexler, D. Heller, M. Kegel, O. Zimmer, W. Hell, O. Schäfer, A. Schnyder, U. Sigrist, F. Spindler; Method for production of 6 dimethyl Amino Methyl-phenyl-cyclohexane 1.3 diols; EP 20080003846 (29.02.2008); WO 2009/106335
12.

D. Heller, H.-J. Drexler, A. Preetz, A. Torrens, H. Buschmann, M. Garcia, (Esteve), “Rhodium-phosphorus complexes and their use in ring opening reactions”; EP 07380349.6 (12.12.2007)

11.

D. Heller, H.-J. Drexler, A. Preetz, A. Torrens, M. Garcia, (Esteve), Microwave-assisted ring opening reaction”; EP 07380350.4 (12.12.2007). WO 2009074497

10.W. Hell, M. Kegel, H. Buschmann, F. Spindler, D. Heller, H.-J. Drexler, (Gruenenthal GmbH, Germany); Verfahren zur Herstellung substituierter Dimethyl-(3-aryl-butyl)-amin-Verbindungen mittels homogener Katalyse; DE102005052588 (02.11.2005); WO2007051576

9.

A. Preetz, D. Heller, H.-J. Drexler, DE102005037649.5 (05.08.2005) „Homogene katalytische Hydrierung“.

8.

A. Torrens, H. Buschmann, D. Heller, H.-J. Drexler, (Esteve) EP 1674465 (27.12.2004) „Verfahren zur Gewinnung der Enatiomeren der Thienylazolylalkoxyethanaminen“.

7.

A. Torrens, H. Buschmann, D. Heller, H.-J. Drexler, (Esteve) EP04380274.3 (27.12.2004) „Verfahren zur Herstellung von Cizolirtine und dessen Enantiomeren“.

6.

W. Hell, M. Kegel, B. Akteries, H. Buschmann, J. Holenz, H. Löbbermann, D. Heller, H.-J. Drexler, S. Gladow, DE 10326097.8 (06.06.2003) „Verfahren zur Herstellung von Dimethyl-(3-aryl-butyl)-aminverbindungen“ (Grünenthal/Fluka) WO2004108658

5.

D. Heller, H.-J. Drexler, J. You, S. Zhang, DE 10235916.4 (26.07.2002). „E-isomere ß-aromatisch oder heteroaromatisch substituierte ß-Acylaminoacrylate und Verfahren zu deren Herstellung“  WO 2004011414

4.

D. Heller, W. Baumann, DE 102 02 173 (17.1.2002) „Gaseinleitungseinsatz sowie Gaseinleitungsapparatur zur Verfolgung von Reaktionen in flüssiger Phase unter Beteiligung gasförmiger Reaktionspartner mittels Kernresonanz-Spektroskopie (NMR) unter stationären Bedingungen“

3.

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“

2.

D. Röttger, M. Beller, R. Jackstell, D. Heller, H.-J. Drexler, H. Klein, K.-D. Wiese (Oxeno Olefinchemie GmbH); DE 10100708 (10.01.2001) „Neue N-Phenylpyrrolbisphosphanverbindungen und deren Metallkomplexe“ , WO 02055528

1.

B. Heller, W. Schulz, G. Oehme, D. Heller, DE 41 42 247 (17.12.1991); „Verfahren zur selektiven katalytischen Mischcyclisierung von Acetylen mit Nitrilen“