Harald Gröger - Publications

Affiliations: 
Department of Chemistry Universität Bielefeld, Bielefeld, North Rhine-Westphalia, Germany 

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Year Citation  Score
2020 Schober L, Sako M, Takizawa S, Gröger H, Sasai H. Catalytic and enantioselective oxa-Piancatelli reaction using a chiral vanadium complex. Chemical Communications (Cambridge, England). PMID 32735309 DOI: 10.1039/D0Cc02621B  0.44
2019 Hyseni M, Zumbrägel N, Offermanns H, Gröger H. Expanding the Scope of Asinger Chemistry towards Enantiomerically Pure Secondary Amines and β-Aminothiols through Chemoenzymatic Derivatization of 3-Thiazolines Chemistry: a European Journal. 1: 180-191. DOI: 10.3390/Chemistry1010012  0.36
2019 Zumbrägel N, Wagner K, Weißing N, Gröger H. Biocatalytic Reduction of 2‐Monosubstituted 3‐Thiazolines Using Imine Reductases Journal of Heterocyclic Chemistry. 56: 788-794. DOI: 10.1002/Jhet.3437  0.36
2018 Zumbrägel N, Gröger H. One-pot synthesis of a 3-thiazolidine through combination of an Asinger-type multi-component-condensation reaction with an enzymatic imine reduction. Journal of Biotechnology. 291: 35-40. PMID 30579889 DOI: 10.1016/J.Jbiotec.2018.12.009  0.36
2018 Zumbrägel N, Machui P, Nonnhoff J, Gröger H. Enantioselective Biocatalytic Reduction of 2 H-1,4-Benzoxazines using Imine Reductases. The Journal of Organic Chemistry. PMID 30562025 DOI: 10.1021/Acs.Joc.8B02867  0.36
2018 Sako M, Aoki T, Zumbrägel N, Schober L, Gröger H, Takizawa S, Sasai H. Chiral Dinuclear Vanadium Complex-mediated Oxidative Coupling of Resorcinols. The Journal of Organic Chemistry. PMID 30501179 DOI: 10.1021/Acs.Joc.8B02494  0.44
2018 Zumbrägel N, Gröger H. Merging Heterocyclic Chemistry and Biocatalysis in One-Pot Processes through Compartmentalization of the Reaction Steps. Bioengineering (Basel, Switzerland). 5. PMID 30071637 DOI: 10.3390/Bioengineering5030060  0.36
2018 Zumbrägel N, Merten C, Huber SM, Gröger H. Enantioselective reduction of sulfur-containing cyclic imines through biocatalysis. Nature Communications. 9: 1949. PMID 29769523 DOI: 10.1038/S41467-018-03841-5  0.36
2017 Biermann M, Bakonyi D, Hummel W, Gröger H. Design of recombinant whole-cell catalysts for double reduction of CC and CO bonds in enals and application in the synthesis of Guerbet alcohols as industrial bulk chemicals for lubricants Green Chemistry. 19: 405-410. DOI: 10.1039/C6Gc01668E  0.4
2017 Reimer A, Wedde S, Staudt S, Schmidt S, Höffer D, Hummel W, Kragl U, Bornscheuer UT, Gröger H. Process Development through Solvent Engineering in the Biocatalytic Synthesis of the Heterocyclic Bulk Chemical ε-Caprolactone Journal of Heterocyclic Chemistry. 54: 391-396. DOI: 10.1002/Jhet.2595  0.4
2016 Bulut D, Duangdee N, Groeger H, Berkessel A, Hummel W. Screening, molecular cloning and biochemical characterization of an alcohol dehydrogenase from Pichia pastoris useful for the kinetic resolution of a racemic β-hydroxy ketone. Chembiochem : a European Journal of Chemical Biology. PMID 27123855 DOI: 10.1002/Cbic.201600101  0.4
2016 Zumbrägel N, Wetzl D, Iding H, Gröger H. Process Development of Imine Reductase-Catalyzed Enantioselective Synthesis of Cyclic Amines Chemie Ingenieur Technik. 88: 1251-1251. DOI: 10.1002/Cite.201650109  0.36
2016 Biermann M, Gruß H, Hummel W, Gröger H. Guerbet Alcohols: From Processes under Harsh Conditions to Synthesis at Room Temperature under Ambient Pressure Chemcatchem. 8: 895-899. DOI: 10.1002/Cctc.201501241  0.4
2015 Takizawa S, Gröger H, Sasai H. Vanadium in asymmetric synthesis: emerging concepts in catalyst design and applications. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 8992-7. PMID 25809123 DOI: 10.1002/Chem.201406444  0.44
2015 Heidlindemann M, Hammel M, Scheffler U, Mahrwald R, Hummel W, Berkessel A, Gröger H. Chemoenzymatic synthesis of vitamin B5-intermediate (R)-pantolactone via combined asymmetric organo- and biocatalysis. The Journal of Organic Chemistry. 80: 3387-96. PMID 25710713 DOI: 10.1021/Jo502667X  0.4
2015 Bulut D, Gröger H, Hummel W. Development of a growth-dependent selection system for identification of L-threonine aldolases. Applied Microbiology and Biotechnology. 99: 5875-83. PMID 25616526 DOI: 10.1007/S00253-014-6333-Z  0.4
2015 Schmidt S, Scherkus C, Muschiol J, Menyes U, Winkler T, Hummel W, Gröger H, Liese A, Herz HG, Bornscheuer UT. An enzyme cascade synthesis of ε-caprolactone and its oligomers. Angewandte Chemie (International Ed. in English). 54: 2784-7. PMID 25597635 DOI: 10.1002/Anie.201410633  0.4
2015 Metzner R, Hummel W, Wetterich F, König B, Gröger H. Integrated Biocatalysis in Multistep Drug Synthesis without Intermediate Isolation: A de Novo Approach toward a Rosuvastatin Key Building Block Organic Process Research and Development. 19: 635-638. DOI: 10.1021/Acs.Oprd.5B00057  0.4
2015 Reß T, Hummel W, Hanlon SP, Iding H, Gröger H. The Organic–Synthetic Potential of Recombinant Ene Reductases: Substrate-Scope Evaluation and Process Optimization Chemcatchem. 7: 1302-1311. DOI: 10.1002/Cctc.201402903  0.4
2015 Böhm P, Gröger H. Iron(III)‐porphyrin Complex FeTSPP: A Versatile Water‐soluble Catalyst for Oxidations in Organic Syntheses, Biorenewables Degradation and Environmental Applications Chemcatchem. 7: 22-28. DOI: 10.1002/Cctc.201402331  0.36
2015 Schmidt S, Scherkus C, Muschiol J, Menyes U, Winkler T, Hummel W, Gröger H, Liese A, Herz HG, Bornscheuer UT. Eine Enzymkaskade zur Synthese von ε‐Caprolacton und dessen Oligomeren Angewandte Chemie. 127: 2825-2828. DOI: 10.1002/Ange.201410633  0.4
2015 Sato H, Hummel W, Gröger H. Kooperative Katalyse nicht‐kompatibler Katalysatoren durch Kompartimentierung: Wacker‐Oxidation und enzymatische Reduktion in einem Eintopf‐Verfahren im wässrigen Medium Angewandte Chemie. 127: 4570-4574. DOI: 10.1002/Ange.201409590  0.4
2014 Hummel W, Gröger H. Strategies for regeneration of nicotinamide coenzymes emphasizing self-sufficient closed-loop recycling systems. Journal of Biotechnology. 191: 22-31. PMID 25102236 DOI: 10.1016/J.Jbiotec.2014.07.449  0.4
2014 Gröger H, Hummel W. Combining the 'two worlds' of chemocatalysis and biocatalysis towards multi-step one-pot processes in aqueous media. Current Opinion in Chemical Biology. 19: 171-9. PMID 24709123 DOI: 10.1016/J.Cbpa.2014.03.002  0.4
2014 List B, Pupo G, Heidlindemann M, Rulli G, Berkessel A, Hummel W, Gröger H. Combining Asymmetric Organo- and Biocatalysis via Compartmentalization Synfacts. 10: 428-428. DOI: 10.1055/S-0033-1341035  0.4
2014 Heidlindemann M, Rulli G, Berkessel A, Hummel W, Gröger H. Combination of asymmetric organo- and biocatalytic reactions in organic media using immobilized catalysts in different compartments Acs Catalysis. 4: 1099-1103. DOI: 10.1021/Cs4010387  0.4
2014 Greschner W, Lanzerath C, Reß T, Tenbrink K, Borchert S, Mix A, Hummel W, Gröger H. Artificial cofactor regeneration with an iron(III)porphyrin as NADH-oxidase mimic in the enzymatic oxidation of l-glutamate to α-ketoglutarate Journal of Molecular Catalysis B-Enzymatic. 103: 10-15. DOI: 10.1016/J.Molcatb.2013.12.015  0.4
2014 Winkler T, Gröger H, Hummel W. Inside Cover: Enantioselective Rearrangement Coupled with Water Addition: Direct Synthesis of Enantiomerically Pure Saturated Carboxylic Acids from α,β-Unsaturated Aldehydes (ChemCatChem 4/2014) Chemcatchem. 6: 898-898. DOI: 10.1002/Cctc.201490021  0.4
2014 Winkler T, Gröger H, Hummel W. Enantioselective Rearrangement Coupled with Water Addition: Direct Synthesis of Enantiomerically Pure Saturated Carboxylic Acids from α,β‐Unsaturated Aldehydes Chemcatchem. 6: 961-964. DOI: 10.1002/Cctc.201300764  0.4
2013 Rulli G, Heidlindemann M, Berkessel A, Hummel W, Gröger H. Towards catalyst compartimentation in combined chemo- and biocatalytic processes: immobilization of alcohol dehydrogenases for the diastereoselective reduction of a β-hydroxy ketone obtained from an organocatalytic aldol reaction. Journal of Biotechnology. 168: 271-6. PMID 24036136 DOI: 10.1016/J.Jbiotec.2013.08.031  0.4
2013 Staudt S, Bornscheuer UT, Menyes U, Hummel W, Gröger H. Direct biocatalytic one-pot-transformation of cyclohexanol with molecular oxygen into ɛ-caprolactone. Enzyme and Microbial Technology. 53: 288-92. PMID 23931696 DOI: 10.1016/J.Enzmictec.2013.03.011  0.4
2013 Burda E, Reß T, Winkler T, Giese C, Kostrov X, Huber T, Hummel W, Gröger H. Highly enantioselective reduction of α-methylated nitroalkenes. Angewandte Chemie (International Ed. in English). 52: 9323-6. PMID 23893708 DOI: 10.1002/Anie.201301814  0.4
2013 Staudt S, Burda E, Giese C, Müller CA, Marienhagen J, Schwaneberg U, Hummel W, Drauz K, Gröger H. Direct oxidation of cycloalkanes to cycloalkanones with oxygen in water. Angewandte Chemie (International Ed. in English). 52: 2359-63. PMID 23339093 DOI: 10.1002/Anie.201204464  0.4
2013 Burda E, Reß T, Winkler T, Giese C, Kostrov X, Huber T, Hummel W, Gröger H. A Highly Enantioselective Route Towards α-Methylated Amines Synfacts. 9: 1347-1347. DOI: 10.1055/S-0033-1340276  0.4
2013 Burda E, Reß T, Winkler T, Giese C, Kostrov X, Huber T, Hummel W, Gröger H. Hochenantioselektive Reduktion von α‐methylierten Nitroalkenen Angewandte Chemie. 125: 9493-9496. DOI: 10.1002/Ange.201301814  0.4
2013 Staudt S, Burda E, Giese C, Müller CA, Marienhagen J, Schwaneberg U, Hummel W, Drauz K, Gröger H. Direktoxidation von Cycloalkanen zu Cycloalkanonen mit Sauerstoff in Wasser Angewandte Chemie. 125: 2415-2419. DOI: 10.1002/Ange.201204464  0.4
2013 Müller CA, Akkapurathu B, Winkler T, Staudt S, Hummel W, Gröger H, Schwaneberg U. In Vitro Double Oxidation of n-Heptane with Direct Cofactor Regeneration Advanced Synthesis & Catalysis. 355: 1787-1798. DOI: 10.1002/Adsc.201300143  0.4
2012 Schnapperelle I, Hummel W, Gröger H. Formal asymmetric hydration of non-activated alkenes in aqueous medium through a "chemoenzymatic catalytic system". Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 1073-6. PMID 22213251 DOI: 10.1002/Chem.201102579  0.4
2012 Borchert S, Burda E, Schatz J, Hummel W, Gröger H. Combination of a Suzuki cross-coupling reaction using a water-soluble palladium catalyst with an asymmetric enzymatic reduction towards a one-pot process in aqueous medium at room temperature Journal of Molecular Catalysis B-Enzymatic. 84: 89-93. DOI: 10.1016/J.Molcatb.2012.03.006  0.4
2011 Rulli G, Duangdee N, Baer K, Hummel W, Berkessel A, Gröger H. Direction of kinetically versus thermodynamically controlled organocatalysis and its application in chemoenzymatic synthesis. Angewandte Chemie (International Ed. in English). 50: 7944-7. PMID 21744441 DOI: 10.1002/Anie.201008042  0.4
2011 Richter N, Gröger H, Hummel W. Asymmetric reduction of activated alkenes using an enoate reductase from Gluconobacter oxydans Applied Microbiology and Biotechnology. 89: 79-89. PMID 20717668 DOI: 10.1007/S00253-010-2793-Y  0.4
2011 Kraußer M, Winkler T, Richter N, Dommer S, Fingerhut A, Hummel W, Gröger H. Cover Picture: Combination of CC Bond Formation by Wittig Reaction and Enzymatic CC Bond Reduction in a One‐Pot Process in Water (ChemCatChem 2/2011) Chemcatchem. 3: 237-237. DOI: 10.1002/Cctc.201190004  0.4
2011 Kraußer M, Winkler T, Richter N, Dommer S, Fingerhut A, Hummel W, Gröger H. Combination of CC Bond Formation by Wittig Reaction and Enzymatic CC Bond Reduction in a One‐Pot Process in Water Chemcatchem. 3: 293-296. DOI: 10.1002/Cctc.201000391  0.4
2011 Maid H, Böhm P, Huber SM, Bauer W, Hummel W, Jux N, Gröger H. Eisenkatalyse zur In‐situ‐Regenerierung oxidierter Cofaktoren durch Aktivierung und Reduktion von O2: ein synthetisches Metalloporphyrin als biomimetische NAD(P)H‐Oxidase Angewandte Chemie. 123: 2445-2448. DOI: 10.1002/Ange.201004101  0.4
2010 Dückers N, Baer K, Simon S, Gröger H, Hummel W. Threonine aldolases-screening, properties and applications in the synthesis of non-proteinogenic beta-hydroxy-alpha-amino acids. Applied Microbiology and Biotechnology. 88: 409-24. PMID 20683718 DOI: 10.1007/S00253-010-2751-8  0.4
2010 Weckbecker A, Gröger H, Hummel W. Regeneration of nicotinamide coenzymes: principles and applications for the synthesis of chiral compounds. Advances in Biochemical Engineering/Biotechnology. 120: 195-242. PMID 20182929 DOI: 10.1007/10_2009_55  0.4
2010 Parkot J, Gröger H, Hummel W. Purification, cloning, and overexpression of an alcohol dehydrogenase from Nocardia globerula reducing aliphatic ketones and bulky ketoesters. Applied Microbiology and Biotechnology. 86: 1813-20. PMID 20054534 DOI: 10.1007/S00253-009-2385-X  0.4
2010 Neupert A, Ress T, Wittmann J, Hummel W, Gröger H. Enantioselective Biocatalytic Reduction of Non-protected Hydroxyacetophenones Zeitschrift FüR Naturforschung B. 65: 337-340. DOI: 10.1515/Znb-2010-0317  0.4
2010 Baer K, Kraußer M, Burda E, Hummel W, Berkessel A, Gröger H. Combining Organo- and Biocatalysis Synfacts. 2010: 99-99. DOI: 10.1055/S-0029-1218488  0.4
2010 Baer K, Dückers N, Hummel W, Gröger H. Expanding the Application Range of Aldolases: Novel Asymmetric Syntheses of α‐Methylated β‐Hydroxy α‐Amino Acids and β‐Amino Alcohols Chemcatchem. 2: 939-942. DOI: 10.1002/Cctc.201000007  0.4
2010 Burda E, Bauer W, Hummel W, Gröger H. Enantio‐ and Diastereoselective Chemoenzymatic Synthesis of C2‐Symmetric Biaryl‐Containing Diols Chemcatchem. 2: 67-72. DOI: 10.1002/Cctc.200900156  0.4
2009 Baer K, Krausser M, Burda E, Hummel W, Berkessel A, Gröger H. Sequential and modular synthesis of chiral 1,3-diols with two stereogenic centers: access to all four stereoisomers by combination of organo- and biocatalysis. Angewandte Chemie (International Ed. in English). 48: 9355-8. PMID 19902444 DOI: 10.1002/Anie.200900582  0.4
2009 Burda E, Kraußer M, Fischer G, Hummel W, Müller‐Uri F, Kreis W, Gröger H. Recombinant Δ4,5‐Steroid 5 β‐Reductases as Biocatalysts for the Reduction of Activated CC‐Double Bonds in Monocyclic and Acyclic Molecules Advanced Synthesis & Catalysis. 351: 2787-2790. DOI: 10.1002/Adsc.200900024  0.4
2008 Burda E, Hummel W, Gröger H. Modular chemoenzymatic one-pot syntheses in aqueous media: combination of a palladium-catalyzed cross-coupling with an asymmetric biotransformation. Angewandte Chemie (International Ed. in English). 47: 9551-4. PMID 18942686 DOI: 10.1002/Anie.200801341  0.4
2008 Burda E, Hummel W, Gröger H. Modulare chemoenzymatische Eintopfsynthesen im wässrigen Medium: Kombination einer Palladium-katalysierten Kreuzkupplung mit einer asymmetrischen Biotransformation Angewandte Chemie. 120: 9693-9696. DOI: 10.1002/Ange.200801341  0.4
2008 Gröger H, Wilken J, Berkessel A. Simple Amino Acids and Short-Chain Peptides as Efficient Metal-Free Catalysts in Asymmetric Synthesis Organic Synthesis Set. 178-186. DOI: 10.1002/9783527620784.Ch18D  0.4
2007 Kraußer M, Hummel W, Gröger H. Enantioselective one-pot two-step synthesis of hydrophobic allylic alcohols in aqueous medium through the combination of a wittig reaction and an enzymatic ketone reduction European Journal of Organic Chemistry. 2007: 5175-5179. DOI: 10.1002/Ejoc.200700647  0.4
2006 Gröger H, Chamouleau F, Orologas N, Rollmann C, Drauz K, Hummel W, Weckbecker A, May O. Enantioselective reduction of ketones with "designer cells" at high substrate concentrations: highly efficient access to functionalized optically active alcohols. Angewandte Chemie (International Ed. in English). 45: 5677-81. PMID 16858704 DOI: 10.1002/Anie.200503394  0.4
2006 Gröger H, Chamouleau F, Orologas N, Rollmann C, Drauz K, Hummel W, Weckbecker A, May O. Biocatalytic Asymmetric Reduction of Ketones Using Designer Cells Synfacts. 2006: 1169-1169. DOI: 10.1055/S-2006-949461  0.4
2006 Gröger H, Chamouleau F, Orologas N, Rollmann C, Drauz K, Hummel W, Weckbecker A, May O. Enantioselektive Ketonreduktion mit “Designerzellen” bei hohen Substratkonzentrationen: hocheffizienter Zugang zu funktionalisierten optisch aktiven Alkoholen† Angewandte Chemie. 118: 5806-5809. DOI: 10.1002/Ange.200503394  0.4
2004 Gröger H, Hummel W, Rollmann C, Chamouleau F, Hüsken H, Werner H, Wunderlich C, Abokitse K, Drauz K, Buchholz S. Preparative asymmetric reduction of ketones in a biphasic medium with an (S)-alcohol dehydrogenase under in situ-cofactor-recycling with a formate dehydrogenase Tetrahedron. 60: 633-640. DOI: 10.1016/J.Tet.2003.11.066  0.4
2003 Gröger H, Hummel W, Buchholz S, Drauz K, Nguyen TV, Rollmann C, Hüsken H, Abokitse K. Practical asymmetric enzymatic reduction through discovery of a dehydrogenase-compatible biphasic reaction media. Organic Letters. 5: 173-6. PMID 12529133 DOI: 10.1021/Ol0272139  0.4
2003 Hummel W, Abokitse K, Drauz K, Rollmann C, Gröger H. Towards a Large‐Scale Asymmetric Reduction Process with Isolated Enzymes: Expression of an (S)‐Alcohol Dehydrogenase in E. coli and Studies on the Synthetic Potential of this Biocatalyst Advanced Synthesis & Catalysis. 345: 153-159. DOI: 10.1002/Adsc.200390064  0.4
2001 Gröger H, Wilken J. The Application of L-Proline as an Enzyme Mimic and Further New Asymmetric Syntheses Using Small Organic Molecules as Chiral Catalysts. Angewandte Chemie (International Ed. in English). 40: 529-532. PMID 11180360 DOI: 10.1002/1521-3773(20010202)40:3<529::Aid-Anie529>3.0.Co;2-X  0.4
2001 Manickam G, Nogami H, Kanai M, Gröger H, Shibasaki M. Anti- and Syn-Selective Cyanosilylation Reactions Promoted by a Sugar-Based Bifunctional Catalyst: Stereoselective Syntheses of Essential Building Blocks for HIV Protease Inhibitors and Bestatin Synlett. 2001: 617-620. DOI: 10.1055/S-2001-13383  0.56
2001 Gröger H, Wilken J. Die Anwendung von L-Prolin als Enzymmimetikum und weitere neue asymmetrische Synthesen mit kleinen organischen Molekülen als chiralen Katalysatoren Angewandte Chemie. 113: 545-548. DOI: 10.1002/1521-3757(20010202)113:3<545::Aid-Ange545>3.0.Co;2-J  0.4
2000 Schlemminger I, Saida Y, Gröger H, Maison W, Durot N, Sasai H, Shibasaki M, Martens J. Concept of improved rigidity: how to make enantioselective hydrophosphonylation of cyclic imines catalyzed by chiral heterobimetallic lanthanoid complexes almost perfect Journal of Organic Chemistry. 65: 4818-4825. PMID 10956457 DOI: 10.1021/Jo991882R  0.56
2000 Gröger H, Goerlich JR, Schmutzler R, Martens J. The First Synthesis of a 2H-1,4-Benzothiazine-based Phosphine Oxide and Sulfide Phosphorus Sulfur and Silicon and the Related Elements. 166: 253-259. DOI: 10.1080/10426500008076546  0.52
1999 Vogl EM, Gröger H, Shibasaki M. Towards Perfect Asymmetric Catalysis: Additives and Cocatalysts. Angewandte Chemie (International Ed. in English). 38: 1570-1577. PMID 29711000 DOI: 10.1002/(Sici)1521-3773(19990601)38:11<1570::Aid-Anie1570>3.0.Co;2-Y  0.56
1999 Yamada K, Harwood SJ, Gröger H, Shibasaki M. The First Catalytic Asymmetric Nitro-Mannich-Type Reaction Promoted by a New Heterobimetallic Complex. Angewandte Chemie. 38: 3504-3506. PMID 10602222 DOI: 10.1002/(Sici)1521-3773(19991203)38:23<3504::Aid-Anie3504>3.0.Co;2-E  0.56
1998 Gröger H, Wilken J, Martens J, Neda I, Schmutzler R. The first synthesis of cyclic ?-amino phosphonic acid amides bearing the benzodiazaphosphorinanone system Heteroatom Chemistry. 9: 679-686. DOI: 10.1002/(Sici)1098-1071(1998)9:7<679::Aid-Hc13>3.0.Co;2-#  0.52
1997 Gröger H, Martens J, Goerlich JR, Schmutzler R. A NOVEL SYNTHETIC APPROACH TO α-AMINOPHOSPHINE SULFIDE STRUCTURES: THE FIRST ADDITION OF DIMETHYL-PHOSPHINE SULFIDE TO 3-THIAZOLINES Phosphorus Sulfur and Silicon and the Related Elements. 128: 153-163. DOI: 10.1080/10426509708031571  0.52
1997 Wilken J, Gröger H, Kossenjans M, Martens J. Synthesis and application of new (threo)- and (erythro)-amino alcohols based on the octahydro-cyclopenta[b]pyrrole system in the catalytic enantioselective addition of diethylzinc to benzaldehyde Tetrahedron-Asymmetry. 8: 2007-2015. DOI: 10.1016/S0957-4166(97)00327-3  0.52
1997 Reiners I, Gröger H, Martens J. A New Enantioselective Synthetic Approach to β-Aminothio-Compounds via enantioselective reduction of N,S-heterocyclic imines† Journal Fur Praktische Chemie-Chemiker-Zeitung. 339: 541-546. DOI: 10.1002/Prac.19973390197  0.52
1997 Gröger H, Tehranfar D, Martens J, Goerlich JR, Thönnessen H, Jones PG, Schmutzler R. Synthesis of dimethyl 4‐thiazolidinylphosphine oxides via addition of dimethylphosphine oxide to 3‐thiazolines Heteroatom Chemistry. 8: 207-215. DOI: 10.1002/(Sici)1098-1071(1997)8:3<207::Aid-Hc3>3.0.Co;2-9  0.52
1996 Gröger H, Wilken J, Martens J. Stereoselektive Pudovik-Reaktion von 5,6-Benzo-2//-l-methyl-3- (2’-chlorethyl)-2-oxo-1,3,2λ4-diazaphosphorin-4-on mit einem 3-Thiazolin und MPL-chromatographische Isolierung des Überschußdiastereomers / Stereoselective Pudovik Reaction of 5,6-Benzo-2H-1-methyl-3-(2’-chloroethyl)-2-oxo-1,3,2λ4-diazaphosphorin-4-one with a 3-Thiazoline and MPL-Chromatographical Isolation of the Major Diastereomer Zeitschrift FüR Naturforschung B. 51: 1305-1312. DOI: 10.1515/Znb-1996-0915  0.52
1996 Gröger H, Manikowski J, Martens J. Synthetic Approach To New Alpha -Aminophosphonates Derived From Six-Membered, Sulfur-Containing Heterocyclic Imines Phosphorus Sulfur and Silicon and the Related Elements. 116: 123-132. DOI: 10.1080/10426509608040475  0.52
1996 Hatam M, Goerlich JR, Schmutzler R, Gröger H, Martens J. The Totally Protected Hydroxy Containing alpha-Amino Phosphonic Esters and alpha-Amino Phosphinoxides as well as their Carbamoyl Derivatives Synthetic Communications. 26: 3685-3698. DOI: 10.1080/00397919608003785  0.52
1996 Gröger H, Hatam M, Kintscher J, Martens J. Synthesis of Glutathione Analogues, Peptide Nucleic Acids and Phosphonooligopeptides from Heterocyclic Imines Synthetic Communications. 26: 3383-3394. DOI: 10.1080/00397919608003741  0.52
1996 Gröger H, Martens J. Synthesis Of New 4-Thiazolidinylphosphonates Via Stereoselective Pudovik Reaction Synthetic Communications. 26: 1903-1911. DOI: 10.1080/00397919608003543  0.52
1995 Gröger H, Hatam M, Martens J. Synthese totalgeschützter, nichtproteinogener α-Aminosäuren und Oligopeptide aus 2H-1,3-Oxazinen und 2H-1,3-Benzoxazinen via Ugi-Reaktion Tetrahedron. 51: 7173-7180. DOI: 10.1016/0040-4020(95)00365-F  0.52
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