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Dieter Enders - Publications

Affiliations: 
Rheinisch-Westfaelische Technische Hochschule, Aachen, NRW, Germany 
Area:
Asymmetric Synthesis, New Synthetic Methods Using Organometallics, Synthesis of Bioactive Compounds, Organocatalysis
Website:
http://www.oc.rwth-aachen.de/akenders/enders_e.html
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Year Citation  Score
2020 Liu Q, Zhang CS, Sheng H, Enders D, Wang ZX, Chen XY. Site-Selective Pyridyl Alkyl Ketone Synthesis from -Alkenoxypyridiniums through Boekelheide-Type Rearrangements. Organic Letters. PMID 32633979 DOI: 10.1021/Acs.Orglett.0C01984  0.544
2020 Vetica F, Bailey SJ, Kumar M, Mahajan S, Essen Cv, Rissanen K, Enders D. Palladium-Catalyzed [3+2] Cycloaddition of Vinylaziridine and Indane-1,3-diones: Diastereo- and Enantioselective Access to Spiro-Pyrrolidines Synthesis. 52: 2038-2044. DOI: 10.1055/S-0040-1707472  0.806
2019 Chen XY, Enders D. Radical Umpolung: Efficient Options for the Synthesis of 1,4-Dicarbonyl Compounds. Angewandte Chemie (International Ed. in English). PMID 30941794 DOI: 10.1002/Anie.201902132  0.418
2019 Chen X, Enders D. Radikalische Umpolung: Effiziente Möglichkeiten zur Synthese von 1,4‐Dicarbonylverbindungen Angewandte Chemie. 131: 6556-6558. DOI: 10.1002/Ange.201902132  0.409
2019 Liu Q, Chen X, Li S, Rissanen K, Enders D. N‐Heterocyclic Carbene Catalyzed Asymmetric Synthesis of Pentacyclic Spirooxindoles via [3+3] Annulations of Isatin‐Derived Enals and Cyclic N‐Sulfonyl Ketimines Advanced Synthesis & Catalysis. 361: 1991-1994. DOI: 10.1002/adsc.201900065  0.477
2018 Chen XY, Li S, Vetica F, Kumar M, Enders D. N-Heterocyclic-Carbene-Catalyzed Domino Reactions via Two or More Activation Modes. Iscience. 2: 1-26. PMID 30428366 DOI: 10.1016/J.Isci.2018.03.006  0.759
2018 Enders D, Liu Q, Chen XY, Puttreddy R, Rissanen K. N-Heterocyclic Carbene Catalyzed Quadruple Domino Reactions through α,β-Unsaturated Acyl Azolium Intermediates: Asymmetric Synthesis of Cyclopenta[c]chromenones. Angewandte Chemie (International Ed. in English). PMID 30394638 DOI: 10.1002/Anie.201810402  0.509
2018 Shu T, Zhao L, Li S, Chen XY, von Essen C, Rissanen K, Enders D. Asymmetric Synthesis of Spirocyclic β-Lactams through Copper-Catalyzed Kinugasa/Michael Domino Reactions. Angewandte Chemie (International Ed. in English). PMID 29968950 DOI: 10.1002/Anie.201806931  0.544
2018 Shu T, Li S, Chen XY, Liu Q, von Essen C, Rissanen K, Enders D. Asymmetric synthesis of functionalized tetrahydrofluorenones via an NHC-catalyzed homoenolate Michael addition. Chemical Communications (Cambridge, England). PMID 29932187 DOI: 10.1039/C8Cc04145H  0.573
2018 Liu Q, Li S, Chen XY, Rissanen K, Enders D. Asymmetric Synthesis of Spiro-oxindole-ε-lactones through N-Heterocyclic Carbene Catalysis. Organic Letters. PMID 29878795 DOI: 10.1021/Acs.Orglett.8B01400  0.524
2018 Enders D, Chen XY, Li S, Liu Q, Kumar M, Peuronen A, Rissanen K. Highly Enantioselective Kinetic Resolution of Michael Adducts through N-Heterocyclic Carbene Catalysis: An Efficient Asymmetric Route to Cyclohexenes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29847691 DOI: 10.1002/Chem.201802420  0.507
2018 Kumar M, Chauhan P, Bailey SJ, Jafari E, von Essen C, Rissanen K, Enders D. Organocatalytic Oxa-Michael/Michael/Michael/Aldol Condensation Quadruple Domino Sequence: Asymmetric Synthesis of Tricyclic Chromanes. Organic Letters. PMID 29406738 DOI: 10.1021/Acs.Orglett.8B00175  0.655
2018 Blümel M, Hack D, Ronkartz L, Vermeeren C, Enders D. Development of an enantioselective amine-silver co-catalyzed Conia-ene reaction. Chemical Communications (Cambridge, England). 53: 3956-3959. PMID 28327700 DOI: 10.1039/C7Cc01807J  0.53
2018 Enders D, Zhao L, Raabe G. Asymmetric Synthesis of 2,2-Disubstituted Benzofuranones through an Organocatalytic Alkylation with Nitroallylic Acetates Synthesis. 51: 1391-1398. DOI: 10.1055/S-0037-1610337  0.553
2018 Zhao L, Li S, Wang L, Yu S, Raabe G, Enders D. Asymmetric Synthesis of Cyclopentene-Fused Tetrahydroquinolines via N-Heterocyclic Carbene Catalyzed Domino Reactions Synthesis. 50: 2523-2532. DOI: 10.1055/S-0036-1591995  0.554
2018 Zhi Y, Zhao K, von Essen C, Rissanen K, Enders D. Synthesis of trans-disubstituted-2,3-dihydrobenzofurans by a formal [4 + 1] annulation between para-quinone methides and sulfonium salts Organic Chemistry Frontiers. 5: 1348-1351. DOI: 10.1039/C8Qo00008E  0.495
2018 Li S, Chen X, Enders D. Aldehyde Catalysis: New Options for Asymmetric Organocatalytic Reactions Chem. 4: 2026-2028. DOI: 10.1016/J.Chempr.2018.08.011  0.491
2018 Chen X, Enders D. Multisubstituted Unnatural Prolines for Asymmetric Catalytic Domino Reactions Chem. 4: 21-23. DOI: 10.1016/J.Chempr.2017.12.007  0.467
2018 Jafari E, Chauhan P, Kumar M, Chen X, Li S, von Essen C, Rissanen K, Enders D. Organocatalytic Asymmetric Synthesis of Trifluoromethylated Tetrahydrocarbazoles by a Vinylogous Michael/Aldol Formal [4+2] Annulation European Journal of Organic Chemistry. 2018: 2462-2465. DOI: 10.1002/Ejoc.201800034  0.54
2018 Chen X, Li S, Liu Q, Kumar M, Peuronen A, Rissanen K, Enders D. Cover Feature: Highly Enantioselective Kinetic Resolution of Michael Adducts through N-Heterocyclic Carbene Catalysis: An Efficient Asymmetric Route to Cyclohexenes (Chem. Eur. J. 39/2018) Chemistry - a European Journal. 24: 9699-9699. DOI: 10.1002/Chem.201803007  0.453
2018 Chen X, Liu Q, Chauhan P, Enders D. Katalyse durch N-heterocyclische Carbene über Azoliumdienolate: eine effiziente Strategie für enantioselektive Funktionalisierungen an entfernten Positionen Angewandte Chemie. 130: 3924-3935. DOI: 10.1002/Ange.201709684  0.52
2017 Enders D, Chen XY, Xiong JW, Liu Q, Li S, Sheng H, von Essen C, Rissanen K. Control of N-Heterocyclic Carbene Catalyzed Switchable Linear and Cycloaddition Reactions of Enals: Asymmetric Synthesis of Oxindole-γ-Amino Acid Derivatives. Angewandte Chemie (International Ed. in English). PMID 29149518 DOI: 10.1002/Ange.201708994  0.54
2017 Enders D, Chen XY, Liu Q, Chauhan P. N-Heterocyclic Carbene Catalysis via Azolium Dienolates: An Efficient Strategy for Enantioselective Remote Functionalizations. Angewandte Chemie (International Ed. in English). PMID 29136320 DOI: 10.1002/Anie.201709684  0.667
2017 Chauhan P, Mahajan S, Enders D. Achieving Molecular Complexity via Stereoselective Multiple Domino Reactions Promoted by a Secondary Amine Organocatalyst. Accounts of Chemical Research. PMID 29125741 DOI: 10.1021/Acs.Accounts.7B00406  0.662
2017 Enders D, Kaya U, Chauhan P, Mahajan S, Deckers K, Valkonen A, Rissanen K. Asymmetric Squaramide Catalyzed Domino aza-Friedel-Crafts/N,O Acetalization Reactions Between 2-Naphthols and Pyrazolinone Ketimines. Angewandte Chemie (International Ed. in English). PMID 29044902 DOI: 10.1002/Anie.201709224  0.663
2017 Liu Q, Chen XY, Li S, Jafari E, Raabe G, Enders D. N-Heterocyclic carbene-catalyzed [4+2] annulation of β-methyl enals and cyclic trifluoromethyl ketimines for the asymmetric synthesis of dihydroquinazolinone derivatives. Chemical Communications (Cambridge, England). PMID 28967650 DOI: 10.1039/C7Cc06562K  0.527
2017 Enders D, Chen XY, Li S, Sheng H, Liu Q, Jafari E, von Essen C, Rissanen K. N-Heterocyclic Carbene Catalyzed [3+2] Cycloaddition of Enals with Masked Cinnamates for the Asymmetric One-Pot Synthesis of Adipic Acid Derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28771855 DOI: 10.1002/Chem.201703579  0.511
2017 Mahajan S, Chauhan P, Kaya U, Deckers K, Rissanen K, Enders D. Enantioselective synthesis of pyrazolone α-aminonitrile derivatives via an organocatalytic Strecker reaction. Chemical Communications (Cambridge, England). PMID 28585622 DOI: 10.1039/C7Cc02874A  0.713
2017 Wang L, Li S, Blümel M, Putreddy R, Peuronen A, Rissanen K, Enders D. Switchable Access to Different Spirocyclopentane Oxindoles via N-Heterocyclic Carbene-Catalyzed Reactions of Isatin-Derived Enals and N-Sulfonyl Ketimines. Angewandte Chemie (International Ed. in English). PMID 28568965 DOI: 10.1002/Anie.201704210  0.542
2017 Chauhan P, Mahajan S, Kaya U, Peuronen A, Rissanen K, Enders D. Asymmetric Synthesis of Amino-Bis-Pyrazolone Derivatives via an Organocatalytic Mannich Reaction. The Journal of Organic Chemistry. PMID 28541704 DOI: 10.1021/Acs.Joc.7B01113  0.703
2017 Kumar M, Chauhan P, Valkonen A, Rissanen K, Enders D. Asymmetric Synthesis of Functionalized Tricyclic Chromanes via an Organocatalytic Triple Domino Reaction. Organic Letters. PMID 28534639 DOI: 10.1021/Acs.Orglett.7B01322  0.709
2017 Chen XY, Liu Q, Chauhan P, Li S, Peuronen A, Rissanen K, Jafari E, Enders D. N-Heterocyclic Carbene Catalyzed [4+2] Annulation of Enals via a Double Vinylogous Michael Addition: Asymmetric Synthesis of 3,5-Diaryl Cyclohexenones. Angewandte Chemie (International Ed. in English). PMID 28429516 DOI: 10.1002/Anie.201702881  0.715
2017 Zhao K, Enders D. Merging N-Heterocyclic Carbene Catalysis and Single Electron Transfer: A New Strategy for Asymmetric Transformations. Angewandte Chemie (International Ed. in English). PMID 28263016 DOI: 10.1002/Anie.201700370  0.354
2017 Vetica F, Chauhan P, Dochain S, Enders D. Asymmetric organocatalytic methods for the synthesis of tetrahydropyrans and their application in total synthesis. Chemical Society Reviews. PMID 28262863 DOI: 10.1039/C6Cs00757K  0.796
2017 Kaya U, Tran UP, Enders D, Ho J, Nguyen TV. N-Heterocyclic Olefin Catalyzed Silylation and Hydrosilylation Reactions of Hydroxyl and Carbonyl Compounds. Organic Letters. PMID 28231015 DOI: 10.1021/Acs.Orglett.7B00306  0.472
2017 Enders D, Li S, Chen X, Sheng H, von Essen C, Rissanen K. N-Heterocyclic Carbene Catalyzed Asymmetric Synthesis of Dihydropyranothiazoles­ via Azolium Enolate Intermediates Synthesis. 50: 1047-1052. DOI: 10.1055/s-0036-1591872  0.492
2017 Enders D, Vetica F, Chauhan P, Mahajan S, Raabe G. Asymmetric Organocatalytic Friedel–Crafts Hydroxyalkylation of Indoles Using Electrophilic Pyrazole-4,5-diones Synthesis. 50: 1039-1046. DOI: 10.1055/S-0036-1591860  0.824
2017 Enders D, Zhao K, Zhi Y, Wang A. Synthesis of Malononitrile-Substituted Diarylmethines via 1,6-Addition of Masked Acyl Cyanides to para-Quinone Methides Synthesis. 50: 872-880. DOI: 10.1055/s-0036-1590947  0.47
2017 Enders D, Jafari E, Kundu D, Chauhan P, Gajulapalli V, von Essen C, Rissanen K. Organocatalytic Enantioselective Vinylogous Henry Reaction of 3,5-Dimethyl-4-nitroisoxazole with Trifluoromethyl Ketones Synthesis. 50: 323-329. DOI: 10.1055/S-0036-1590928  0.678
2017 Enders D, Liu Q, Chen X, Li S, Vetica F, Raabe G. Two-Step Synthesis of α,β-Unsaturated γ-Amino Acid Esters via N-Heterocyclic Carbene Catalyzed [4+2] Cycloaddition of Enals and Nitroso Compounds Synthesis. 50: 127-133. DOI: 10.1055/S-0036-1590901  0.787
2017 Enders D, Gajulapalli V, Jafari E, Kundu D, Mahajan S, Peuronen A, Rissanen K. Organocatalytic Asymmetric Synthesis of 2,3′-Connected Bis-Indolinones by Mannich Reactions of N-Acetylindolin-3-ones with Isatin N-Boc Ketimines Synthesis. 49: 4986-4995. DOI: 10.1055/S-0036-1590823  0.497
2017 Zhi Y, Zhao K, von Essen C, Rissanen K, Enders D. Thiourea-Catalyzed Domino Michael–Mannich [3+2] Cycloadditions: A Strategy for the Asymmetric Synthesis of 3,3′-Pyrrolidinyl-dispirooxindoles Synlett. 28: 2876-2880. DOI: 10.1055/S-0036-1589070  0.53
2017 Enders D, Li S, Chen X, Liu Q, Peuronen A, Rissanen K. N-Heterocyclic Carbene-Catalyzed Activation of α-Chloroaldehydes: Asymmetric Synthesis of 5-Cyano-Substituted Dihydropyranones Synthesis. 49: 4861-4868. DOI: 10.1055/S-0036-1588509  0.538
2017 Liu Q, Zhao K, Zhi Y, Raabe G, Enders D. Squaramide-catalyzed domino Michael/aza-Henry [3 + 2] cycloaddition: asymmetric synthesis of functionalized 5-trifluoromethyl and 3-nitro substituted pyrrolidines Organic Chemistry Frontiers. 4: 1416-1419. DOI: 10.1039/C7Qo00161D  0.564
2017 Lyons DJM, Crocker RD, Enders D, Nguyen TV. Tropylium salts as efficient organic Lewis acid catalysts for acetalization and transacetalization reactions in batch and flow Green Chemistry. 19: 3993-3996. DOI: 10.1039/C7Gc01519D  0.398
2017 Vetica F, Bailey S, Chauhan P, Turberg M, Ghaur A, Raabe G, Enders D. Desymmetrization of Cyclopentenediones via Organocatalytic Cross-Dehydrogenative Coupling Advanced Synthesis & Catalysis. 359: 3729-3734. DOI: 10.1002/Adsc.201700917  0.801
2017 Zhi Y, Zhao K, Wang A, Englert U, Raabe G, Enders D. Asymmetric Synthesis of Cyclopentane-Substituted Oxindoles via Organocatalytic Desymmetrization of Cyclopent-4-ene-1,3-diones Advanced Synthesis & Catalysis. 359: 1867-1871. DOI: 10.1002/Adsc.201700358  0.585
2017 Chauhan P, Kaya U, Enders D. Advances in Organocatalytic 1,6-Addition Reactions: Enantioselective Construction of Remote Stereogenic Centers Advanced Synthesis & Catalysis. 359: 888-912. DOI: 10.1002/Adsc.201601342  0.646
2016 Dochain S, Vetica F, Puttreddy R, Rissanen K, Enders D. Combining Organocatalysis and Lanthanide Catalysis: A Sequential One-Pot Quadruple Reaction Sequence/Hetero-Diels-Alder Asymmetric Synthesis of Functionalized Tricycles. Angewandte Chemie (International Ed. in English). PMID 27879031 DOI: 10.1002/Anie.201610196  0.799
2016 Zhi Y, Zhao K, Liu Q, Wang A, Enders D. Asymmetric synthesis of functionalized trifluoromethyl-substituted pyrrolidines via an organocatalytic domino Michael/Mannich [3+2] cycloaddition. Chemical Communications (Cambridge, England). PMID 27853768 DOI: 10.1039/C6Cc08352H  0.524
2016 Zhao K, Zhi Y, Shu T, Valkonen A, Rissanen K, Enders D. Organocatalytic Domino Oxa-Michael/1,6-Addition Reactions: Asymmetric Synthesis of Chromans Bearing Oxindole Scaffolds. Angewandte Chemie (International Ed. in English). PMID 27600477 DOI: 10.1002/Anie.201606947  0.554
2016 Wang L, Li S, Blümel M, Philipps AR, Wang A, Puttreddy R, Rissanen K, Enders D. Asymmetric Synthesis of Spirobenzazepinones with Atroposelectivity and Spiro-1,2-Diazepinones by NHC-Catalyzed [3+4] Annulation Reactions. Angewandte Chemie (International Ed. in English). PMID 27436702 DOI: 10.1002/Anie.201604819  0.54
2016 Blümel M, Crocker RD, Harper JB, Enders D, Nguyen TV. N-Heterocyclic olefins as efficient phase-transfer catalysts for base-promoted alkylation reactions. Chemical Communications (Cambridge, England). PMID 27251600 DOI: 10.1039/C6Cc03771B  0.449
2016 Blümel M, Noy JM, Enders D, Stenzel MH, Nguyen TV. Development and Applications of Transesterification Reactions Catalyzed by N-Heterocyclic Olefins. Organic Letters. PMID 27115463 DOI: 10.1021/Acs.Orglett.6B00835  0.465
2016 Enders D, Wang L, Li S, Chauhan P, Hack D, Philipps AR, Puttreddy R, Rissanen KT, Raabe G. Asymmetric Three Component One-Pot Synthesis of Spiropyrazolones and 2,5-Chromene-diones via Aldol Condensation/NHC-Catalyzed Annulation Reactions. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26864437 DOI: 10.1002/Chem.201600515  0.688
2016 Shu T, Ni Q, Song X, Zhao K, Wu T, Puttreddy R, Rissanen K, Enders D. Asymmetric synthesis of cyclopentanes bearing four contiguous stereocenters via an NHC-catalyzed Michael/Michael/esterification domino reaction. Chemical Communications (Cambridge, England). PMID 26750327 DOI: 10.1039/C5Cc09581F  0.588
2016 Zhao K, Zhi Y, Li X, Puttreddy R, Rissanen K, Enders D. Asymmetric synthesis of 3,3'-pyrrolidinyl-dispirooxindoles via a one-pot organocatalytic Mannich/deprotection/aza-Michael sequence. Chemical Communications (Cambridge, England). PMID 26725839 DOI: 10.1039/c5cc10057g  0.424
2016 List B, Grossmann O, Zhao K, Zhi Y, Shu T, Valkonen A, Rissanen K, Enders D. Asymmetric Synthesis of Chromans Bearing Oxindole Scaffolds Synfacts. 12: 1305-1305. DOI: 10.1055/S-0036-1589633  0.481
2016 Enders D, Bröhl N, Kundu D, Raabe G. One-Pot Synthesis of 1-Substituted 1H-Isochromenes by Combining Brønsted Acid with Silver Catalysis Synthesis. 49: 1243-1254. DOI: 10.1055/S-0036-1588641  0.478
2016 Li S, Wang L, Chauhan P, Peuronen A, Rissanen K, Enders D. Asymmetric Synthesis of Five-Membered Spiropyrazolones via N-Heterocyclic Carbene (NHC)-Catalyzed [3+2] Annulations Synthesis. 49: 1808-1815. DOI: 10.1055/S-0036-1588381  0.693
2016 Enders D, Philipps A, Blümel M, Dochain S, Hack D. Enantioselective Catalytic One-Pot Synthesis of Functionalized Methyleneindanes and Methylindenes via a Michael/Conia-Ene Sequence Synthesis. 49: 1538-1546. DOI: 10.1055/S-0036-1588113  0.504
2016 Enders D, Vetica F, Fronert J, Puttreddy R, Rissanen K. Asymmetric Organocatalytic Synthesis of 4-Aminoisochromanones via a Direct One-Pot Intramolecular Mannich Reaction Synthesis. 48: 4451-4458. DOI: 10.1055/S-0035-1562522  0.806
2016 Kaya U, Mahajan S, Schöbel JH, Valkonen A, Rissanen K, Enders D. Diastereoselective Synthesis of Spiro[pyrazolone-4,3′-tetrahydrothiophenes] via a Sulfa-Michael/Aldol Domino Reaction Synthesis (Germany). DOI: 10.1055/S-0035-1562473  0.536
2016 Kaya U, Chauhan P, Deckers K, Puttreddy R, Rissanen K, Raabe G, Enders D. Asymmetric Synthesis of Tetrahydrobenzofurans and Annulated Dihydropyrans via Cooperative One-Pot Organo- and Silver-Catalysis Synthesis. 48: 3207-3216. DOI: 10.1055/S-0035-1561468  0.681
2016 Mahajan S, Chauhan P, Blümel M, Puttreddy R, Rissanen K, Raabe G, Enders D. Asymmetric Synthesis of Spiro Tetrahydrothiophene-indan-1,3-diones via a Squaramide-Catalyzed Sulfa-Michael/Aldol Domino Reaction Synthesis (Germany). DOI: 10.1055/S-0035-1560412  0.702
2016 Zhao K, Zhi Y, Wang A, Enders D. Asymmetric Organocatalytic Synthesis of 3-Diarylmethine-Substituted Oxindoles Bearing a Quaternary Stereocenter via 1,6-Conjugate Addition to para-Quinone Methides Acs Catalysis. 6: 657-660. DOI: 10.1021/acscatal.5b02519  0.462
2016 Chauhan P, Mahajan S, Kaya U, Valkonen A, Rissanen K, Enders D. Asymmetric Synthesis of Spiro β-Lactamsviaa Squaramide- Catalyzed Sulfa-Michael Addition/Desymmetrization Protocol Advanced Synthesis & Catalysis. 358: 3173-3178. DOI: 10.1002/Adsc.201600554  0.662
2015 Ni Q, Xiong J, Song X, Raabe G, Enders D. N-Heterocyclic Carbene Catalyzed Enantioselective Annulation of Benzothiazolyl Ethyl Acetates with 2-Bromoenals. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 26: 1465-1469. PMID 26752810 DOI: 10.1055/s-0034-1381004  0.439
2015 Philipps AR, Fritze L, Erdmann N, Enders D. An Asymmetric Organocatalytic Quadruple Domino Reaction Employing a Vinylogous Friedel-Crafts/Michael/Michael/Aldol Condensation Sequence. Synthesis. 47: 2377-2384. PMID 26752794 DOI: 10.1055/s-0034-1380197  0.41
2015 Mahajan S, Chauhan P, Loh CC, Uzungelis S, Raabe G, Enders D. Organocatalytic Asymmetric Domino Michael/Henry Reaction of Indolin-3-ones with o-Formyl-β-nitrostyrenes. Synthesis. 47: 1024-1031. PMID 26722133 DOI: 10.1055/S-0034-1379943  0.627
2015 Hahn R, Jafari E, Raabe G, Enders D. Organocatalytic Asymmetric Synthesis of Dihydroisoquinolinones via a One-Pot Aza-Henry-Hemiaminalization-Oxidation Sequence. Synthesis. 47: 472-480. PMID 26722132 DOI: 10.1055/s-0034-1379398  0.373
2015 Hack D, Dürr AB, Deckers K, Chauhan P, Seling N, Rübenach L, Mertens L, Raabe G, Schoenebeck F, Enders D. Asymmetric Synthesis of Spiropyrazolones by Sequential Organo- and Silver Catalysis. Angewandte Chemie (International Ed. in English). PMID 26676875 DOI: 10.1002/Anie.201510602  0.685
2015 Kaya U, Chauhan P, Hack D, Deckers K, Puttreddy R, Rissanen K, Enders D. Enantioselective synthesis of 4H-pyranonaphthoquinones via sequential squaramide and silver catalysis. Chemical Communications (Cambridge, England). PMID 26660230 DOI: 10.1039/C5Cc09592A  0.635
2015 Ni Q, Xiong J, Song X, Raabe G, Enders D. NHC-catalyzed activation of α,β-unsaturated N-acyltriazoles: an easy access to dihydropyranones. Chemical Communications (Cambridge, England). 51: 14628-31. PMID 26287399 DOI: 10.1039/c5cc06044c  0.314
2015 Chauhan P, Mahajan S, Enders D. Asymmetric synthesis of pyrazoles and pyrazolones employing the reactivity of pyrazolin-5-one derivatives. Chemical Communications (Cambridge, England). 51: 12890-907. PMID 26178319 DOI: 10.1039/C5Cc04930J  0.667
2015 Hack D, Blümel M, Chauhan P, Philipps AR, Enders D. Catalytic Conia-ene and related reactions. Chemical Society Reviews. 44: 6059-93. PMID 26031492 DOI: 10.1039/C5Cs00097A  0.661
2015 Wang L, Ni Q, Blümel M, Shu T, Raabe G, Enders D. NHC-Catalyzed Asymmetric Synthesis of Functionalized Succinimides from Enals and α-Ketoamides. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 8033-7. PMID 25877658 DOI: 10.1002/Chem.201500661  0.514
2015 Zhao K, Shu T, Jia J, Raabe G, Enders D. An organocatalytic Mannich/denitration reaction for the asymmetric synthesis of 3-ethylacetate-substitued 3-amino-2-oxindoles: formal synthesis of AG-041R. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 3933-6. PMID 25630891 DOI: 10.1002/Chem.201406422  0.539
2015 Hack D, Chauhan P, Deckers K, Mizutani Y, Raabe G, Enders D. Combining silver- and organocatalysis: an enantioselective sequential catalytic approach towards pyrano-annulated pyrazoles. Chemical Communications (Cambridge, England). 51: 2266-9. PMID 25564304 DOI: 10.1039/C4Cc09495F  0.629
2015 Chauhan P, Mahajan S, Raabe G, Enders D. Organocatalytic one-pot 1,4-/1,6-/1,2-addition sequence for the stereocontrolled formation of six consecutive stereocenters. Chemical Communications (Cambridge, England). 51: 2270-2. PMID 25563802 DOI: 10.1039/C4Cc09730K  0.626
2015 Ni Q, Song X, Xiong J, Raabe G, Enders D. Regio- and stereoselective synthesis of benzothiazolo-pyrimidinones via an NHC-catalyzed Mannich/lactamization domino reaction. Chemical Communications (Cambridge, England). 51: 1263-6. PMID 25476422 DOI: 10.1039/c4cc08594a  0.502
2015 Zou LH, Philipps AR, Raabe G, Enders D. Asymmetric synthesis of fully substituted cyclopentane-oxindoles through an organocatalytic triple Michael domino reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 1004-8. PMID 25470781 DOI: 10.1002/chem.201406047  0.434
2015 Blümel M, Chauhan P, Vermeeren C, Dreier A, Lehmann C, Enders D. Asymmetric organocatalytic synthesis of highly functionalized spirocyclohexane indandiones via a one-pot michael/michael/aldol sequence Synthesis (Germany). 47: 3618-3628. DOI: 10.1055/S-0035-1560072  0.708
2015 Beceño C, Krappitz T, Raabe G, Enders D. Asymmetric Synthesis of Tetrahydropyridines via a Bronsted Acid Catalyzed Aza-Diels-Alder Reaction Synthesis (Germany). 47: 3813-3821. DOI: 10.1055/S-0034-1381058  0.547
2015 Ni Q, Xiong J, Song X, Raabe G, Enders D. N-Heterocyclic Carbene Catalyzed Enantioselective Annulation of Benzothiazolyl Ethyl Acetates with 2-Bromoenals Synlett. 26: 1465-1469. DOI: 10.1055/s-0034-1381004  0.366
2015 Philipps AR, Fritze L, Erdmann N, Enders D. An Asymmetric Organocatalytic Quadruple Domino Reaction Employing a Vinylogous Friedel–Crafts/Michael/Michael/Aldol Condensation Sequence Synthesis (Germany). DOI: 10.1055/s-0034-1380197  0.329
2015 Mahajan S, Chauhan P, Loh CCJ, Uzungelis S, Raabe G, Enders D. Organocatalytic Asymmetric Domino Michael/Henry Reaction of Indolin-3-ones with o -Formyl-β-nitrostyrenes Synthesis (Germany). 47: 1024-1031. DOI: 10.1055/s-0034-1379943  0.535
2015 Chauhan P, Mahajan S, Enders D. Asymmetric synthesis of pyrazoles and pyrazolones employing the reactivity of pyrazolin-5-one derivatives Chemical Communications. 51: 12890-12907. DOI: 10.1039/c5cc04930j  0.631
2015 Chauhan P, Mahajan S, Raabe G, Enders D. Organocatalytic one-pot 1,4-/1,6-/1,2-addition sequence for the stereocontrolled formation of six consecutive stereocenters Chemical Communications. 51: 2270-2272. DOI: 10.1039/c4cc09730k  0.467
2015 Hack D, Chauhan P, Deckers K, Mizutani Y, Raabe G, Enders D. Combining silver- and organocatalysis: An enantioselective sequential catalytic approach towards pyrano-annulated pyrazoles Chemical Communications. 51: 2266-2269. DOI: 10.1039/c4cc09495f  0.517
2015 Zou LH, Philipps AR, Raabe G, Enders D. Asymmetric synthesis of fully substituted cyclopentane-oxindoles through an organocatalytic triple Michael domino reaction Chemistry - a European Journal. 21: 1004-1008. DOI: 10.1002/chem.201406047  0.47
2015 Beceño C, Chauhan P, Rembiak A, Wang A, Enders D. Brønsted acid-catalyzed enantioselective synthesis of isatin- derived N,S-acetals Advanced Synthesis and Catalysis. 357: 672-676. DOI: 10.1002/Adsc.201401155  0.65
2015 Chauhan P, Mahajan S, Kaya U, Hack D, Enders D. Bifunctional amine-squaramides: Powerful hydrogen-bonding organocatalysts for asymmetric domino/cascade reactions Advanced Synthesis and Catalysis. 357: 253-281. DOI: 10.1002/Adsc.201401003  0.606
2014 Song X, Ni Q, Zhu C, Raabe G, Enders D. Asymmetric N-Heterocyclic Carbene Catalyzed Annulation of 2-Alkenylbenzothiazoles with α-Chloro Aldehydes. Synthesis. 47: 421-428. PMID 26752795 DOI: 10.1055/s-0034-1379369  0.474
2014 Blümel M, Chauhan P, Hahn R, Raabe G, Enders D. Asymmetric synthesis of tetrahydropyridines via an organocatalytic one-pot multicomponent Michael/aza-Henry/cyclization triple domino reaction. Organic Letters. 16: 6012-5. PMID 25379786 DOI: 10.1021/Ol503024D  0.703
2014 Urbanietz G, Atodiresei I, Enders D. Asymmetric Synthesis of Functionalized Dihydro- and Tetrahydropyrans via an Organocatalytic Domino Michael-Hemiacetalization Reaction. Synthesis. 46: 1261-1269. PMID 25284900 DOI: 10.1055/s-0033-1340826  0.448
2014 Joie C, Deckers K, Enders D. Organocatalytic Asymmetric Synthesis of Functionalized 1,3,5-Triarylpyrrolidin-2-ones via an Aza-Michael/Aldol Domino Reaction. Synthesis. 46: 799-808. PMID 25278634 DOI: 10.1055/s-0033-1340565  0.429
2014 Joie C, Deckers K, Raabe G, Enders D. An Asymmetric Organocatalytic Quadruple Cascade to Tetraaryl-Substituted 2-Azabicyclo[3.3.0]octadienones. Synthesis. 46: 1539-1546. PMID 25278633 DOI: 10.1055/s-0033-1340982  0.465
2014 Hack D, Chauhan P, Deckers K, Hermann GN, Mertens L, Raabe G, Enders D. Combining silver catalysis and organocatalysis: a sequential Michael addition/hydroalkoxylation one-pot approach to annulated coumarins. Organic Letters. 16: 5188-91. PMID 25250728 DOI: 10.1021/Ol502551U  0.672
2014 Chauhan P, Mahajan S, Enders D. Organocatalytic carbon-sulfur bond-forming reactions. Chemical Reviews. 114: 8807-64. PMID 25144663 DOI: 10.1021/Cr500235V  0.498
2014 Hahn R, Raabe G, Enders D. Asymmetric synthesis of highly functionalized tetrahydropyrans via a one-pot organocatalytic Michael/Henry/ketalization sequence. Organic Letters. 16: 3636-9. PMID 24971998 DOI: 10.1021/Ol501236A  0.496
2014 Chauhan P, Urbanietz G, Raabe G, Enders D. Asymmetric synthesis of functionalized cyclohexanes bearing five stereocenters via a one-pot organocatalytic Michael-Michael-1,2-addition sequence. Chemical Communications (Cambridge, England). 50: 6853-5. PMID 24842728 DOI: 10.1039/C4Cc01885K  0.633
2014 Chauhan P, Mahajan S, Loh CCJ, Raabe G, Enders D. Streocontrolled construction of six vicinal stereogenic centers on spiropyrazolones via organocascade michael/michael/1,2-addition reactions Organic Letters. 16: 2954-2957. PMID 24840166 DOI: 10.1021/Ol501093V  0.694
2014 Ni Q, Song X, Raabe G, Enders D. N-heterocyclic carbene-catalyzed enantioselective annulation of indolin-3-ones with bromoenals. Chemistry, An Asian Journal. 9: 1535-8. PMID 24729588 DOI: 10.1002/asia.201402052  0.434
2014 Enders D, Stöckel BA, Rembiak A. Enantio- and chemoselective Brønsted-acid/Mg(nBu) 2 catalysed reduction of α-keto esters with catecholborane Chemical Communications. 50: 4489-4491. PMID 24643455 DOI: 10.1039/C4Cc00427B  0.464
2014 Hack D, Loh CC, Hartmann JM, Raabe G, Enders D. Merging gold and organocatalysis: a facile asymmetric synthesis of annulated pyrroles. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 3917-21. PMID 24590817 DOI: 10.1002/chem.201400407  0.401
2014 Chauhan P, Enders D. N-heterocyclic carbene catalyzed activation of esters: a new option for asymmetric domino reactions. Angewandte Chemie (International Ed. in English). 53: 1485-7. PMID 24492969 DOI: 10.1002/Anie.201309952  0.646
2014 Song X, Ni Q, Zhu C, Raabe G, Enders D. Asymmetric N-heterocyclic carbene catalyzed annulation of 2-alkenylbenzothiazoles with α-chloro aldehydes Synthesis (Germany). 46. DOI: 10.1055/s-0034-1379369  0.362
2014 Joie C, Deckers K, Raabe G, Enders D. An asymmetric Organocatalytic quadruple cascade to tetraaryl-substituted 2-azabicyclo[33.0]octadienones Synthesis (Germany). 46: 1539-1546. DOI: 10.1055/s-0033-1340982  0.407
2014 Urbanietz G, Atodiresei I, Enders D. Asymmetric synthesis of functionalized dihydro- and tetrahydropyrans via an organocatalytic domino Michael-hemiacetalization reaction Synthesis (Germany). 46: 1261-1269. DOI: 10.1055/s-0033-1340826  0.419
2014 Joie C, Deckers K, Enders D. Organocatalytic asymmetric synthesis of functionalized 1,3,5- triarylpyrrolidin-2-ones via an aza-Michael/aldol domino reaction Synthesis (Germany). 46: 799-808. DOI: 10.1055/s-0033-1340565  0.429
2014 Chauhan P, Urbanietz G, Raabe G, Enders D. Asymmetric synthesis of functionalized cyclohexanes bearing five stereocenters via a one-pot organocatalytic Michael-Michael-1,2-addition sequence Chemical Communications. 50: 6853-6855. DOI: 10.1039/c4cc01885k  0.578
2014 Chauhan P, Mahajan S, Enders D. Organocatalytic carbon-sulfur bond-forming reactions Chemical Reviews. 114: 8807-8864. DOI: 10.1021/cr500235v  0.498
2014 Karimi B, Jafari E, Enders D. Asymmetric mannich reaction of malonates with aldimines using YbIII-pybox complexes supported on self-assembled organic-inorganic hybrid silica with an imidazolium framework European Journal of Organic Chemistry. 2014: 7253-7258. DOI: 10.1002/Ejoc.201402713  0.402
2014 Ni Q, Song X, Raabe G, Enders D. N-heterocyclic carbene-catalyzed enantioselective annulation of indolin-3-ones with bromoenals Chemistry - An Asian Journal. 9: 1535-1538. DOI: 10.1002/asia.201402052  0.356
2014 Chauhan P, Enders D. N-heterocyclic carbene catalyzed activation of esters: A new option for asymmetric domino reactions Angewandte Chemie - International Edition. 53: 1485-1487. DOI: 10.1002/anie.201309952  0.612
2014 Chauhan P, Enders D. Durch N-heterocyclische Carbene katalysierte Aktivierung von Estern: eine Option für asymmetrische Dominoreaktionen Angewandte Chemie. 126: 1509-1511. DOI: 10.1002/Ange.201309952  0.516
2014 Loh CCJ, Chauhan P, Hack D, Lehmann C, Enders D. Rapid asymmetric synthesis of highly functionalized indanols via a Michael/Henry organocascade with submol% squaramide catalyst loadings Advanced Synthesis and Catalysis. 356: 3181-3186. DOI: 10.1002/Adsc.201400499  0.528
2013 Ni Q, Zhang H, Grossmann A, Loh CC, Merkens C, Enders D. Asymmetric synthesis of pyrroloindolones by N-heterocyclic carbene catalyzed [2+3] annulation of α-chloroaldehydes with nitrovinylindoles. Angewandte Chemie (International Ed. in English). 52: 13562-6. PMID 24346939 DOI: 10.1002/anie.201305957  0.428
2013 Loh CC, Hack D, Enders D. Asymmetric domino synthesis of indanes bearing four contiguous stereocentres catalyzed by sub-mol% loadings of a squaramide in minutes. Chemical Communications (Cambridge, England). 49: 10230-2. PMID 24064746 DOI: 10.1039/C3Cc46033A  0.474
2013 Song X, Ni Q, Grossmann A, Enders D. N-heterocyclic-carbene-catalyzed one-pot synthesis of hydroxamic esters. Chemistry, An Asian Journal. 8: 2965-9. PMID 24027246 DOI: 10.1002/asia.201300938  0.42
2013 Enders D, Joie C, Deckers K. Organocatalytic asymmetric synthesis of tetracyclic pyridocarbazole derivatives by using a Diels-Alder/aza-Michael/aldol condensation domino reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 10818-21. PMID 23813770 DOI: 10.1002/chem.201302127  0.468
2013 Karimi B, Jafari E, Enders D. Highly efficient catalytic enantioselective mannich reaction of malonates with N-tert-butoxycarbonyl imines by using Yb(OTf)3/pybox catalysts at room temperature Chemistry - a European Journal. 19: 10142-10145. PMID 23787963 DOI: 10.1002/Chem.201300241  0.489
2013 Zeng X, Ni Q, Raabe G, Enders D. A branched domino reaction: asymmetric organocatalytic two-component four-step synthesis of polyfunctionalized cyclohexene derivatives. Angewandte Chemie (International Ed. in English). 52: 2977-80. PMID 23355486 DOI: 10.1002/Anie.201209581  0.526
2013 Enders D, Grossmann A, Van Craen D. N-Heterocyclic carbene catalyzed synthesis of oxime esters Organic and Biomolecular Chemistry. 11: 138-141. PMID 23104187 DOI: 10.1039/c2ob26974k  0.478
2013 Enders D, Del Signore G, Raabe G. Asymmetric synthesis of α-(heteroaryl)alkylamines and α-amino acids via nucleophilic 1,2-addition of lithiated heterocycles to aldehyde SAMP-hydrazones Turkish Journal of Chemistry. 37: 492-518. DOI: 10.3906/Kim-1302-71  0.546
2013 Yamamoto H, Ano Y, Karimi B, Jafari E, Enders D. Ytterbium-Catalyzed Enantioselective Mannich Reaction of Malonates Synfacts. 9: 1076-1076. DOI: 10.1055/S-0033-1339783  0.565
2013 Hack D, Enders D. Asymmetric organocatalytic Michael addition of pyrroles to enones by cinchona alkaloid-derived primary amines Synthesis (Germany). 45: 2904-2912. DOI: 10.1055/s-0033-1339546  0.363
2013 Fronert J, Bisschops T, Cassens-Sasse E, Atodiresei I, Enders D. Asymmetric organocatalytic synthesis of trans -3,4-disubstituted isochromanones via an intramolecular aldol reaction Synthesis (Germany). 45: 1708-1712. DOI: 10.1055/s-0033-1338742  0.46
2013 Nguyen TV, Hartmann JM, Enders D. Recent synthetic strategies to access seven-membered carbocycles in natural product synthesis Synthesis (Germany). 45: 845-873. DOI: 10.1055/S-0032-1318152  0.476
2013 Enders D, Reichenbach LF. Asymmetric synthesis of synargentolide A and its 3-epimer using the RAMP-hydrazone methodology Synthesis (Germany). 45: 959-965. DOI: 10.1055/S-0032-1316865  0.536
2013 Enders D, Rembiak A, Seppelt M. Asymmetric organocatalytic reduction of ketimines with catecholborane employing a N-triflyl phosphoramide Brønsted acid as catalyst Tetrahedron Letters. 54: 470-473. DOI: 10.1016/J.Tetlet.2012.11.055  0.472
2013 Takizawa S, Nguyen TMN, Grossmann A, Suzuki M, Enders D, Sasai H. Facile synthesis of α-methylidene-γ-butyrolactones: Intramolecular Rauhut-Currier reaction promoted by chiral acid-base organocatalysts Tetrahedron. 69: 1202-1209. DOI: 10.1016/J.Tet.2012.11.046  0.42
2013 Ansari S, Raabe G, Enders D. Asymmetric Michael addition of 1,3-bis(phenylthio)propan-2-one to nitroalkenes employing Takemoto's thiourea catalyst Monatshefte Fur Chemie. 144: 641-646. DOI: 10.1007/S00706-012-0915-1  0.495
2013 Enders D, Rembiak A, Stoeckel BA. ChemInform Abstract: Chemo- and Enantioselective Broensted Acid-Catalyzed Reduction of α-Imino Esters with Catecholborane. Cheminform. 44: no-no. DOI: 10.1002/chin.201352053  0.327
2013 Enders D, Joie C, Deckers K. Organocatalytic asymmetric synthesis of tetracyclic pyridocarbazole derivatives by using a diels-alder/aza-michael/aldol condensation domino reaction Chemistry - a European Journal. 19: 10818-10821. DOI: 10.1002/chem.201302127  0.468
2013 Song X, Ni Q, Grossmann A, Enders D. N-heterocyclic-carbene-catalyzed one-pot synthesis of hydroxamic esters Chemistry - An Asian Journal. 8: 2965-2969. DOI: 10.1002/asia.201300938  0.42
2013 Ni Q, Zhang H, Grossmann A, Loh CCJ, Merkens C, Enders D. Asymmetric synthesis of pyrroloindolones by N-heterocyclic carbene catalyzed [2+3] annulation of α-chloroaldehydes with nitrovinylindoles Angewandte Chemie - International Edition. 52: 13562-13566. DOI: 10.1002/anie.201305957  0.408
2013 Zeng X, Ni Q, Raabe G, Enders D. A branched domino reaction: Asymmetric organocatalytic two-component four-step synthesis of polyfunctionalized cyclohexene derivatives Angewandte Chemie - International Edition. 52: 2977-2980. DOI: 10.1002/anie.201209581  0.433
2013 Ni Q, Zhang H, Grossmann A, Loh CCJ, Merkens C, Enders D. Asymmetrische Synthese von Pyrroloindolonen über eine durch N-heterocyclische Carbene katalysierte [2+3]-Anellierung von α-Chloraldehyden mit Nitrovinylindolen† Angewandte Chemie. 125: 13806-13811. DOI: 10.1002/Ange.201305957  0.374
2013 Enders D, Rembiak A, Stöckel BA. Chemo- and enantioselective Brønsted acid-catalyzed reduction of α-imino esters with catecholborane Advanced Synthesis and Catalysis. 355: 1937-1942. DOI: 10.1002/Adsc.201300352  0.488
2013 Enders D, Hahn R, Atodiresei I. Asymmetric Synthesis of Functionalized Tetrahydronaphthalenes via an Organocatalytic Nitroalkane-Michael/Henry Domino Reaction Advanced Synthesis and Catalysis. 355: 1126-1136. DOI: 10.1002/adsc.201300039  0.413
2013 Erdmann N, Philipps AR, Atodiresei I, Enders D. An asymmetric organocatalytic quadruple cascade initiated by a Friedel-Crafts-type reaction with electron-rich arenes Advanced Synthesis and Catalysis. 355: 847-852. DOI: 10.1002/Adsc.201201099  0.47
2012 Enders D, Fronert J, Bisschops T, Boeck F. Asymmetric total synthesis of smyrindiol employing an organocatalytic aldol key step. Beilstein Journal of Organic Chemistry. 8: 1112-7. PMID 23019438 DOI: 10.3762/Bjoc.8.123  0.564
2012 Loh CCJ, Raabe G, Enders D. Enantioselective synthesis of tetrahydrocarbazoles through a Michael addition/Ciamician-Plancher rearrangement sequence: Asymmetric synthesis of a potent constrained analogue of MS-245 Chemistry - a European Journal. 18: 13250-13254. PMID 22976923 DOI: 10.1002/Chem.201202908  0.436
2012 Wan JP, Loh CC, Pan F, Enders D. Enantioselective organocatalytic domino synthesis of tetrahydropyridin-2-ols. Chemical Communications (Cambridge, England). 48: 10049-51. PMID 22948095 DOI: 10.1039/c2cc35644a  0.44
2012 Enders D, Greb A, Deckers K, Selig P, Merkens C. Quadruple domino organocatalysis: an asymmetric aza-Michael/Michael/Michael/aldol reaction sequence leading to tetracyclic indole structures with six stereocenters. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 10226-9. PMID 22865412 DOI: 10.1002/Chem.201201493  0.441
2012 Enders D, Grossmann A, Gieraths B, Düzdemir M, Merkens C. Organocatalytic one-pot asymmetric synthesis of 4 H,5 H-pyrano[2,3-c] pyrazoles Organic Letters. 14: 4254-4257. PMID 22852800 DOI: 10.1021/Ol301983F  0.518
2012 Wang C, Yang X, Loh CCJ, Raabe G, Enders D. Organocatalytic, asymmetric synthesis of 3-sulfenylated N-Boc-protected oxindoles Chemistry - a European Journal. 18: 11531-11535. PMID 22836361 DOI: 10.1002/chem.201201262  0.348
2012 Enders D, Nguyen TV. Chiral quaternary phosphonium salts: a new class of organocatalysts. Organic & Biomolecular Chemistry. 10: 5327-31. PMID 22707074 DOI: 10.1039/C2Ob25823D  0.331
2012 Loh CC, Enders D. Merging organocatalysis and gold catalysis--a critical evaluation of the underlying concepts. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 10212-25. PMID 22696311 DOI: 10.1002/Chem.201200287  0.363
2012 Takizawa S, Nguyen TM, Grossmann A, Enders D, Sasai H. Enantioselective synthesis of α-alkylidene-γ-butyrolactones: intramolecular Rauhut-Currier reaction promoted by acid/base organocatalysts. Angewandte Chemie (International Ed. in English). 51: 5423-6. PMID 22511309 DOI: 10.1002/Anie.201201542  0.507
2012 Wang C, Yang X, Enders D. Asymmetric Michael addition of N-boc-protected oxindoles to nitroalkenes catalyzed by a chiral secondary amine. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 4832-5. PMID 22434659 DOI: 10.1002/chem.201200079  0.38
2012 Enders D, Ludwig M, Raabe G. Synthesis and application of the first planar chiral strong Brønsted acid organocatalysts. Chirality. 24: 215-22. PMID 22278775 DOI: 10.1002/Chir.21985  0.55
2012 Grossmann A, Enders D. N-heterocyclic carbene catalyzed domino reactions. Angewandte Chemie (International Ed. in English). 51: 314-25. PMID 22121084 DOI: 10.1002/anie.201105415  0.356
2012 Enders D, Fronert J, Bisschops T, Boeck F. Asymmetric total synthesis of smyrindiol employing an organocatalytic aldol key step Beilstein Journal of Organic Chemistry. 8: 1112-1117. DOI: 10.3762/bjoc.8.123  0.399
2012 Enders D, David S, Deckers K, Greb A, Raabe G. Asymmetric synthesis of gonioheptolide A analogues via an organocatalytic aldol reaction as the key step Synthesis (Germany). 44: 3483-3488. DOI: 10.1055/S-0032-1316803  0.584
2012 Yang X, Wang C, Ni Q, Enders D. Secondary-amine-catalyzed asymmetric Michael addition of N-tert-butoxycarbonyl-protected oxindoles to maleimides Synthesis (Germany). 44: 2601-2606. DOI: 10.1055/s-0032-1316577  0.344
2012 Erdmann N, Atodiresei I, Enders D. Asymmetric synthesis of 3-substituted hexahydro-3H-isochromenes via an organocatalytic triple cascade/Yb-catalyzed hetero-Diels-Alder sequence Synthesis (Germany). 44: 2107-2113. DOI: 10.1055/s-0031-1290374  0.341
2012 Enders D, Urbanietz G, Hahn R, Raabe G. Asymmetric synthesis of functionalized chromans via a one-pot organocatalytic domino Michael-hemiacetalization or -lactonization and dehydration sequence Synthesis. 44: 773-782. DOI: 10.1055/S-0031-1289683  0.427
2012 Enders D, Nguyen TV. Secondary amine catalyzed retro-aldol reactions of enals and enones: One-pot conversion of enals to α-substituted derivatives Tetrahedron Letters. 53: 2091-2095. DOI: 10.1016/j.tetlet.2012.02.039  0.448
2012 Enders D, Ludwig M, Raabe G. Synthesis and application of the first planar chiral strong brønsted acid organocatalysts Chirality. 24: 215-222. DOI: 10.1002/chir.21985  0.324
2012 Enders D, Greb A, Deckers K, Selig P, Merkens C. Quadruple domino organocatalysis: An asymmetric aza-Michael/Michael/ Michael/Aldol reaction sequence leading to tetracyclic indole structures with six stereocenters Chemistry - a European Journal. 18: 10226-10229. DOI: 10.1002/chem.201201493  0.33
2012 Wang C, Yang X, Enders D. Asymmetric michael addition of N-Boc-protected oxindoles to nitroalkenes catalyzed by a chiral secondary amine Chemistry - a European Journal. 18: 4832-4835. DOI: 10.1002/chem.201200079  0.381
2012 Grossmann A, Enders D. N-heterocyclic carbene catalyzed domino reactions Angewandte Chemie - International Edition. 51: 314-325. DOI: 10.1002/anie.201105415  0.356
2012 Wang C, Yang X, Raabe G, Enders D. A short asymmetric synthesis of the benzopyrano[3,4-c]pyrrolidine core via an organocatalytic domino oxa-michael/michael reaction Advanced Synthesis and Catalysis. 354: 2629-2634. DOI: 10.1002/adsc.201200472  0.376
2012 Enders D, Urbanietz G, Cassens-Sasse E, Keeß S, Raabe G. Control of six contiguous stereocenters in an asymmetric organocatalytic one-pot Michael/Michael/aldol addition sequence Advanced Synthesis and Catalysis. 354: 1481-1488. DOI: 10.1002/Adsc.201200120  0.514
2011 Loh CCJ, Badorrek J, Raabe G, Enders D. Merging organocatalysis and gold catalysis: Enantioselective synthesis of tetracyclic indole derivatives through a sequential double Friedel-Crafts type reaction Chemistry - a European Journal. 17: 13409-13414. PMID 22025408 DOI: 10.1002/chem.201102793  0.431
2011 Alachraf MW, Handayani PP, Hüttl MRM, Grondal C, Enders D, Schrader W. Electrospray mass spectrometry for detailed mechanistic studies of a complex organocatalyzed triple cascade reaction Organic and Biomolecular Chemistry. 9: 1047-1053. PMID 21152637 DOI: 10.1039/C003433A  0.381
2011 Enders D, Yang X, Wang C, Raabe G, Runsik J. Controlling the Reaction Mechanism to Construct Dihydrocoumarins Synfacts. 2011: 1011-1011. DOI: 10.1055/S-0030-1260924  0.334
2011 Enders D, Urbanietz G, Raabe G. Organocatalytic asymmetric synthesis of functionalized 4 H -chromenes via a one-pot Domino Michael-Hemiacetalization and dehydration sequence Synthesis. 1905-1911. DOI: 10.1055/S-0030-1260017  0.514
2011 Enders D, Wang C, Yang X, Raabe G. One-pot organocatalytic asymmetric synthesis of 1H-pyrrolo[1,2a]indol-3(2H) -ones via a Michael-hemiaminalization-oxidation sequence Synlett. 469-472. DOI: 10.1055/S-0030-1259326  0.376
2011 Enders D, Seppelt M. Catalytic enantioselective synthesis of 3-substituted benzosultams via Corey-Bakshi-Shibata reduction of cyclic N-sulfonylimines Synlett. 402-404. DOI: 10.1055/S-0030-1259314  0.543
2011 Enders D. Synthesis: Editorial Synthesis. DOI: 10.1055/s-0030-1258378  0.359
2011 Enders D, Rembiak A, Liebich JX. Direct organocatalytic -sulfenylation of aldehydes and ketones with tetramethylthiuram disulfide Synthesis. 281-286. DOI: 10.1055/S-0030-1258359  0.47
2011 Enders D, Grossmann A, Huang H, Raabe G. Dual secondary amine/N-heterocyclic carbene catalysis in the asymmetric Michael/cross-benzoin cascade reaction of β-oxo sulfones with enals European Journal of Organic Chemistry. 4298-4301. DOI: 10.1002/ejoc.201100690  0.35
2010 Grondal C, Jeanty M, Enders D. Organocatalytic cascade reactions as a new tool in total synthesis. Nature Chemistry. 2: 167-78. PMID 21124474 DOI: 10.1038/Nchem.539  0.49
2010 Enders D, Grossmann A, Fronert J, Raabe G. N-heterocyclic carbene catalysed asymmetric cross-benzoin reactions of heteroaromatic aldehydes with trifluoromethyl ketones Chemical Communications. 46: 6282-6284. PMID 20694237 DOI: 10.1039/C0Cc02013C  0.534
2010 Enders D, Liebich JX, Raabe G. Organocatalytic asymmetric synthesis of trans-1,3-disubstituted tetrahydroisoquinolines via a reductive amination/aza-Michael sequence. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 9763-6. PMID 20661970 DOI: 10.1002/chem.201001623  0.373
2010 Enders D, Wang C, Mukanova M, Greb A. Organocatalytic asymmetric synthesis of polyfunctionalized 3-(cyclohexenylmethyl)-indoles via a quadruple domino Friedel-Crafts-type/Michael/Michael/aldol condensation reaction. Chemical Communications (Cambridge, England). 46: 2447-9. PMID 20309466 DOI: 10.1039/c002839h  0.448
2010 Enders D, Terteryan V, Paleek J. Asymmetric synthesis of the α-D-galactosyl ceramide KRN7000 via an organocatalytic aldol reaction as key step Synthesis. 2979-2984. DOI: 10.1055/S-0029-1218844  0.523
2010 Enders D, Schmid B, Erdmann N, Raabe G. Asymmetric synthesis of thiadecalins via an organocatalytic triple cascade/sulfa-michael sequence Synthesis. 2271-2277. DOI: 10.1055/S-0029-1218804  0.496
2010 Enders D, Krüll R, Bettray W. Microwave-assisted organocatalytic quadruple domino reactions of acetaldehyde and nitroalkenes Synthesis. 567-572. DOI: 10.1055/S-0029-1217146  0.506
2010 Enders D, Vazquez J. ChemInform Abstract: Asymmetric Synthesis of α-Substituted β-Formyl δ-Lactones via a Michael Addition/α-Alkylation Protocol. Cheminform. 30: no-no. DOI: 10.1002/chin.199937137  0.318
2010 ENDERS D, MEYER I, RUNSINK J, RAABE G. ChemInform Abstract: Diastereoselective 1,3-Dipolar Cycloadditions with Enantiopure Azomethine Ylids. Cheminform. 29: no-no. DOI: 10.1002/chin.199850141  0.347
2010 ENDERS D, THOMAS CR, RAABE G, RUNSINK J. ChemInform Abstract: Enantioselective Synthesis of α-Substituted N-Methyl-sulfonamides. Cheminform. 29: no-no. DOI: 10.1002/chin.199839057  0.364
2010 ENDERS D, BETTRAY W, SCHANKAT J, WIEDEMANN J. ChemInform Abstract: Diastereo- and Enantioselective Synthesis of β-Amino Acids via SAMP Hydrazones and Hetero Michael Addition Using TMS-SAMP as a Chiral Equivalent of Ammonia Cheminform. 28: no-no. DOI: 10.1002/chin.199746319  0.346
2010 ENDERS D, CHELAIN E, RAABE G. ChemInform Abstract: Enantioselective Synthesis of 1,2-Diamines via Nucleophilic 1,2- Addition to Dibenzylamino-acetaldehyde-SAMP-hydrazone. Cheminform. 28: no-no. DOI: 10.1002/chin.199746088  0.463
2010 ENDERS D, LOCHTMAN R. ChemInform Abstract: Diastereo- and Enantioselective Synthesis of Protected 1,1′-Bis(1- aminoalkyl)ferrocenes via 1,2-Addition of Alkyllithium Compounds to Ferrocene-1,1′-dicarbaldehyde-bis-SAMP-hydrazone. Cheminform. 28: no-no. DOI: 10.1002/chin.199742214  0.335
2010 ENDERS D, WIEDEMANN J. ChemInform Abstract: Diastereo- and Enantioselective Synthesis of Vicinal Diamines via Aza- Michael Addition to Nitroalkenes. Cheminform. 28: no-no. DOI: 10.1002/chin.199722064  0.462
2010 ENDERS D, BREUER K, RUNSINK J, TELES JH. ChemInform Abstract: The First Asymmetric Intramolecular Stetter Reaction. Cheminform. 28: no-no. DOI: 10.1002/chin.199704154  0.367
2010 ENDERS D, BREUER K, TELES JH. ChemInform Abstract: A Novel Asymmetric Benzoin Reaction Catalyzed by a Chiral Triazolium Salt. Cheminform. 27: no-no. DOI: 10.1002/chin.199637047  0.441
2010 ENDERS D, BERG T, RAABE G, RUNSINK J. ChemInform Abstract: Enantioselective Synthesis of α-Phosphinoketones. Cheminform. 27: no-no. DOI: 10.1002/chin.199618166  0.358
2010 ENDERS D, GROEBNER R, RUNSINK J. ChemInform Abstract: Enantioselective Synthesis of 2-Substituted 6- and 7-Membered Lactones via α-Alkylation of Lactone Hydrazones. Cheminform. 26: no-no. DOI: 10.1002/chin.199551040  0.427
2010 ENDERS D. ChemInform Abstract: TMS-SAMP. Novel Chiral Hydrazine Auxiliary for Hetero-Michael Additions and Aza-Peterson Olefinations Cheminform. 26: no-no. DOI: 10.1002/chin.199540308  0.368
2010 ENDERS D. ChemInform Abstract: SADP and SAEP. Novel Chiral Hydrazine Auxiliaries for Asymmetric Synthesis Cheminform. 26: no-no. DOI: 10.1002/chin.199540307  0.409
2010 ENDERS D, SCHANKAT J. ChemInform Abstract: Enantioselective Synthesis of Allyl-, Propargyl-, and 4-En-2-ynyl- amines via 1,2-Addition of Organocerium Reagents to Chiral Aldehyde Imines. Cheminform. 26: no-no. DOI: 10.1002/chin.199538034  0.482
2010 ENDERS D, SCHERER HJ, RUNSINK J. ChemInform Abstract: Diastereo- and Enantioselective Synthesis of 1,2-trans-Substituted Cycloalkanecarboxylates and Sulfones by Michael-Initiated Cyclisation via SAMP/RAMP Hydrazones. Cheminform. 25: no-no. DOI: 10.1002/chin.199424074  0.449
2010 ENDERS D, ZAMPONI A, RAABE G, RUNSINK J. ChemInform Abstract: Enantioselective Synthesis of 2-Alkyl-2-cyanocycloalkanones with a Quaternary Stereogenic Center. Cheminform. 25: no-no. DOI: 10.1002/chin.199415058  0.456
2010 Enders D, Liebich JX, Raabe G. Organocatalytic asymmetric synthesis of trans-1,3-disubstituted tetrahydroisoquinolines via a reductive amination/aza-michael sequence Chemistry - a European Journal. 16: 9763-9766. DOI: 10.1002/chem.201001623  0.373
2010 Enders D, Kipphardt H, Gerdes P, Breña-Valle LJ, Bhushan V. Large scale preparation of versatile chiral auxiliaries derived from (S)-proline1 Bulletin Des SociéTéS Chimiques Belges. 97: 691-704. DOI: 10.1002/Bscb.19880970809  0.422
2010 Enders D, Wang C, Yang X, Raabe G. Asymmetric synthesis of cis-3,4-disubstituted chromans and dihydrocoumarins via an organocatalytic Michael addition/ hemiacetalization reaction Advanced Synthesis and Catalysis. 352: 2869-2874. DOI: 10.1002/adsc.201000659  0.377
2010 Enders D, Göddertz DP, Beceño C, Raabe G. Asymmetric synthesis of polyfunctionalized pyrrolidines via a thiourea catalyzed domino Mannich/aza-Michael reaction Advanced Synthesis and Catalysis. 352: 2863-2868. DOI: 10.1002/Adsc.201000658  0.555
2010 Enders D, Seppelt M, Beck T. Enantioselective organocatalytic synthesis of arylglycines via friedel-crafts alkylation of arenes with a glyoxylate imine Advanced Synthesis and Catalysis. 352: 1413-1418. DOI: 10.1002/adsc.201000143  0.486
2010 Enders D, Wang C, Greb A. Asymmetric synthesis of 2,3,4-trisubstituted functionalised tetrahydrofurans via an organocatalytic michael addition as key step Advanced Synthesis and Catalysis. 352: 987-992. DOI: 10.1002/Adsc.200900879  0.531
2009 Enders D, Wang C, Liebich JX. Organocatalytic asymmetric aza-Michael additions. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 11058-76. PMID 19798719 DOI: 10.1002/chem.200902236  0.349
2009 Enders D, Jeanty M, Bats JW. Organocatalytic asymmetric triple domino reactions of nitromethane with α,β-unsaturated aldehydes Synlett. 3175-3178. DOI: 10.1055/S-0029-1218282  0.479
2009 Enders D, Saeidian H, Mirjafary Z, Iffland D, Raabe G, Runsink J. Diastereo- and enantioselective synthesis of α,β-disubstituted γ-nisalkoxycarbonyl sulfonates Synlett. 2872-2874. DOI: 10.1055/S-0029-1218017  0.478
2009 Enders D, Wang C, Bats JW. Asymmetric synthesis of functionalized 3,4-dihydronaphthalenes via an organocatalytic domino nitroalkane-Michael/aldol condensation reaction Synlett. 1777-1780. DOI: 10.1055/S-0029-1217380  0.566
2009 Enders D, Henseler A, Lowins S. N-heterocyclic carbene catalyzed nucleophilic acylation of trifluoromethyl ketimines Synthesis. 4125-4128. DOI: 10.1055/s-0029-1217070  0.333
2009 Enders D, Wang C, Raabe G. Enantioselective synthesis of 3H-Pyrrolo[1,2-α]indole-2-carbaldehydes via an organocatalytic domino aza-Michael/aldol Condensation reaction Synthesis. 4119-4124. DOI: 10.1055/s-0029-1217069  0.424
2009 Enders D, Iffland D, Raabe G. Asymmetric synthesis of 1,2-anti-disubstituted taurine derivatives Synthesis. 1683-1688. DOI: 10.1055/s-0029-1216643  0.327
2009 Enders D, Jonas EA, Khimpen T. Efficient asymmetric synthesis of Planar-Chiral bisferrocenes European Journal of Organic Chemistry. 2149-2162. DOI: 10.1002/Ejoc.200900015  0.557
2009 Enders D, Henseler A. A direct intermolecular cross-benzoin type reaction: N-heterocyclic carbene-catalyzed coupling of aromatic aldehydes with trifluoromethyl ketones Advanced Synthesis and Catalysis. 351: 1749-1752. DOI: 10.1002/adsc.200900247  0.359
2008 Enders D, Förster D, Raabe G, Bats JW. Asymmetric synthesis of beta-nitro ketones via Michael addition of lithiated alpha-amino nitriles to nitroalkenes. The Journal of Organic Chemistry. 73: 9641-6. PMID 18834175 DOI: 10.1021/Jo8017318  0.44
2008 Enders D, Narine AA. Lessons from nature: biomimetic organocatalytic carbon-carbon bond formations. The Journal of Organic Chemistry. 73: 7857-70. PMID 18778100 DOI: 10.1021/Jo801374J  0.493
2008 Enders D, Han J, Henseler A. Asymmetric intermolecular Stetter reactions catalyzed by a novel triazolium derived N-heterocyclic carbene. Chemical Communications (Cambridge, England). 3989-91. PMID 18758602 DOI: 10.1039/B809913H  0.712
2008 Enders D, Wang C, Bats JW. Organocatalytic asymmetric domino reactions: a cascade consisting of a Michael addition and an aldehyde alpha-alkylation. Angewandte Chemie (International Ed. in English). 47: 7539-42. PMID 18752243 DOI: 10.1002/anie.200802532  0.305
2008 Enders D, Narine AA, Toulgoat F, Bisschops T. Asymmetric Brønsted acid catalyzed isoindoline synthesis: enhancement of enantiomeric ratio by stereoablative kinetic resolution. Angewandte Chemie (International Ed. in English). 47: 5661-5. PMID 18574838 DOI: 10.1002/Anie.200801354  0.462
2008 Enders D, Barbion J. Asymmetric synthesis of (+)-altholactone: a styryllactone isolated from various Goniothalamus species. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 2842-9. PMID 18219645 DOI: 10.1002/chem.200701647  0.373
2008 Enders D, Narine AA, Toulgoat F, Bisschops T. Catalytic Asymmetric Isoindoline Synthesis Synfacts. 2008: 992-992. DOI: 10.1055/S-2008-1078668  0.509
2008 Enders D, Hieronymi A, Raabe G. Asymmetric synthesis of 4′-quaternary 2′-deoxy-3′- and -4′-epi-β-C- and -N-nucleosides Synthesis. 1545-1558. DOI: 10.1055/S-2008-1072577  0.463
2008 Enders D, Terteryan V, Paleček J. Asymmetric synthesis of jaspine B (pachastrissamine) via an organocatalytic Aldol reaction as key step Synthesis. 2278-2282. DOI: 10.1055/S-2008-1067142  0.523
2008 Enders D, Noll S, Raabe G, Runsink J. Synthesis of all possible stereoisomers of α-branched [2.2]paracyclophanylalkylamines Synthesis. 1288-1296. DOI: 10.1055/S-2008-1042941  0.506
2008 Enders D, Han J. Asymmetric intermolecular Stetter reactions of aromatic heterocyclic aldehydes with arylidenemalonates Synthesis. 3864-3868. DOI: 10.1055/S-0028-1083229  0.753
2008 Enders D, Han J. Synthesis of enantiopure triazolium salts from pyroglutamic acid and their evaluation in the benzoin condensation Tetrahedron Asymmetry. 19: 1367-1371. DOI: 10.1016/J.Tetasy.2008.05.017  0.65
2008 Enders D, Wang C, Bats J. Organokatalytische asymmetrische Dominoreaktionen: eine Kaskade aus Michael-Addition und Aldehyd-α-Alkylierung Angewandte Chemie. 120: 7649-7653. DOI: 10.1002/Ange.200802532  0.37
2008 Enders D, Narine AA, Toulgoat F, Bisschops T. Asymmetrische Brønsted‐Säure‐katalysierte Synthese von Isoindolinen: Steigerung des Enantiomerenverhältnisses durch stereoablative kinetische Racematspaltung Angewandte Chemie. 120: 5744-5748. DOI: 10.1002/Ange.200801354  0.301
2008 Enders D, Hüttl MRM, Raabe G, Bats JW. Asymmetric synthesis of polyfunctionalized mono-, Bi-, and tricyclic carbon frameworks via organocatalytic domino reactions Advanced Synthesis and Catalysis. 350: 267-279. DOI: 10.1002/Adsc.200700396  0.488
2007 Enders D, Hüttl MR, Niemeier O. Biomimetic organocatalytic C-C-bond formations. Ernst Schering Foundation Symposium Proceedings. 45-124. PMID 18642522  0.301
2007 Enders D, Dhulut S, Steinbusch D, Herrbach A. Asymmetric total synthesis of (-)-pironetin employing the SAMP/RAMP hydrazone methodology. Chemistry (Weinheim An Der Bergstrasse, Germany). 13: 3942-9. PMID 17295364 DOI: 10.1002/Chem.200601672  0.431
2007 Enders D, Grondal C, Hüttl MR. Asymmetric organocatalytic domino reactions. Angewandte Chemie (International Ed. in English). 46: 1570-81. PMID 17225236 DOI: 10.1002/Anie.200603129  0.462
2007 Enders D, Hüttl MR, Runsink J, Raabe G, Wendt B. Organocatalytic one-pot asymmetric synthesis of functionalized tricyclic carbon frameworks from a triple-cascade/Diels-Alder sequence. Angewandte Chemie (International Ed. in English). 46: 467-9. PMID 17154207 DOI: 10.1002/Anie.200603434  0.384
2007 Enders D, Milovanovic̀ M. Asymmetrie synthesis of (+)-hinokinin, (+)-dihydrocubebin and cubebin dimethyl ether, a new lignan from Phyllanthus niruri Zeitschrift Fur Naturforschung - Section B Journal of Chemical Sciences. 62: 117-120. DOI: 10.1515/Znb-2007-0117  0.536
2007 Harnying W, Kitisriworaphan W, Pohmakotr M, Enders D. Stereoselective sulfonate aldol reactions: Asymmetric synthesis of α,β-substituted β-hydroxy sulfonates Synlett. 2529-2532. DOI: 10.1055/s-2007-986642  0.331
2007 Enders D, Narine AA, Benninghaus TR, Raabe G. Asymmetric organocatalytic domino reactions of γ-nitroketones and enals Synlett. 1667-1670. DOI: 10.1055/s-2007-984517  0.34
2007 Enders D, Iffland D. Asymmetric synthesis of α-phenyl-γ-hetero-substituted isopropyl sulfonates via diastereoselective ring-opening of γ-sultones Synthesis. 1837-1840. DOI: 10.1055/s-2007-983719  0.36
2007 Enders D, Bonten MH, Raabe G. Organocatalytic asymmetric conjugate nucleophilic glyoxylation Synlett. 885-888. DOI: 10.1055/S-2007-970787  0.524
2007 Enders D, Hüttl M, Runsink J, Raabe G, Wendt B. Catalytic Asymmetric Synthesis of Tricyclic Carbon Frameworks Synfacts. 2007: 0433-0433. DOI: 10.1055/S-2007-968346  0.399
2007 Enders D, Lüttgen K, Narine AA. Asymmetric sulfa-Michael additions Synthesis. 959-980. DOI: 10.1055/S-2007-965968  0.451
2007 Enders D, Peiffer E, Raabe G. Asymmetric synthesis of (S,S)- and (R,R)-2-methylthreitol Synthesis. 1021-1026. DOI: 10.1055/S-2007-965967  0.445
2007 Brehme R, Enders D, Fernandez R, Lassaletta JM. Aldehyde N,N-dialkylhydrazones as neutral acyl anion equivalents: Umpolung of the imine reactivity European Journal of Organic Chemistry. 5629-5660. DOI: 10.1002/Ejoc.200700746  0.353
2007 Enders D, Herriger C. Asymmetric synthesis of 2-trifluoromethyl-1,2,3-triols European Journal of Organic Chemistry. 1085-1090. DOI: 10.1002/Ejoc.200600895  0.538
2007 Enders D, Grondal C, Hüttl MRM. Cover Picture: Asymmetric Organocatalytic Domino Reactions (Angew. Chem. Int. Ed. 10/2007) Angewandte Chemie. 46: 1545-1545. DOI: 10.1002/Anie.200790031  0.42
2007 Enders D, Bonten M, Raabe G. Asymmetrische nucleophile Glyoxylierung durch metallierte α-Aminonitril-Derivate in Michael-Additionen an Nitroalkene Angewandte Chemie. 119: 2364-2367. DOI: 10.1002/Ange.200604802  0.387
2007 Enders D, Hüttl M, Runsink J, Raabe G, Wendt B. Organokatalytische, asymmetrische Eintopf-Synthese von funktionalisierten tricyclischen Kohlenstoffgerüsten durch eine Tripelkaskade/Diels-Alder-Sequenz Angewandte Chemie. 119: 471-473. DOI: 10.1002/Ange.200603434  0.465
2007 Grondal C, Enders D. A direct organocatalytic entry to selectively protected aldopentoses and derivatives Advanced Synthesis and Catalysis. 349: 694-702. DOI: 10.1002/Adsc.200600573  0.474
2007 Enders D, Bettray W. Stoichiometric Asymmetric Synthesis: Development of Novel Enantioselective Synthetic Methods Asymmetric Synthesis With Chemical and Biological Methods. 1-37. DOI: 10.1002/9783527610648.ch1a  0.371
2006 Enders D, Hüttl MR, Grondal C, Raabe G. Control of four stereocentres in a triple cascade organocatalytic reaction. Nature. 441: 861-3. PMID 16778886 DOI: 10.1038/Nature04820  0.525
2006 Karimi B, Enders D. New N-heterocyclic carbene palladium complex/ionic liquid matrix immobilized on silica: application as recoverable catalyst for the Heck reaction. Organic Letters. 8: 1237-40. PMID 16524312 DOI: 10.1021/ol060129z  0.31
2006 Enders D, Palecek J, Grondal C. A direct organocatalytic entry to sphingoids: asymmetric synthesis of D-arabino- and L-ribo-phytosphingosine. Chemical Communications (Cambridge, England). 655-7. PMID 16446841 DOI: 10.1039/B515007H  0.445
2006 Enders D, Niemeier O, Balensiefer T. Asymmetric intramolecular crossed-benzoin reactions by N-heterocyclic carbene catalysis. Angewandte Chemie (International Ed. in English). 45: 1463-7. PMID 16389609 DOI: 10.1002/Anie.200503885  0.45
2006 Grondal C, Enders D. A direct entry to carbasugars: Asymmetric synthesis of 1-epi-(+)-MK7607 Synlett. 3507-3509. DOI: 10.1055/s-2006-956495  0.361
2006 Enders D, Niemeier O, Straver L. Asymmetric organocatalytic synthesis of cis-substituted dihydrobenzofuranols via intramolecular aldol reactions Synlett. 3399-3402. DOI: 10.1055/s-2006-956454  0.41
2006 Enders D, Niemeier O, Raabe G. Asymmetric synthesis of chromanones via N-heterocyclic carbene catalyzed intramolecular crossed-benzoin reactions Synlett. 2431-2434. DOI: 10.1055/s-2006-950403  0.431
2006 Enders D, Grondal C, Vrettou M. Efficient entry to amino sugars and derivatives via asymmetric organocatalytic Mannich reactions Synthesis. 3597-3604. DOI: 10.1055/S-2006-942542  0.493
2006 Enders D, Vrettou M. Asymmetric synthesis of (+)-polyoxamic acid via an efficient organocatalytic mannich reaction as the key step Synthesis. 2155-2158. DOI: 10.1055/S-2006-942413  0.531
2006 Enders D, Hüttl M, Grondal C, Raabe G. Triple Cascade Reaction Leading to Tetra-Substituted Cyclohexenes Synfacts. 2006: 0847-0847. DOI: 10.1055/S-2006-942029  0.458
2006 Enders D, Paleček J, Grondal C. Organocatalytic Synthesis of Sphingoids Synfacts. 2006: 273-273. DOI: 10.1055/S-2006-931991  0.475
2006 Enders D, Niemeier O, Balensiefer T. Intramolecular Crossed-Benzoin Reactions Catalyzed by Chiral Triazolium Salts Synfacts. 2006: 283-283. DOI: 10.1055/S-2006-931989  0.481
2006 Enders D, Tedeschi L, Förster D. Asymmetric Michael additions of a chiral phosphite to nitroalkenes and knoevenagel acceptors Synthesis. 1447-1460. DOI: 10.1055/S-2006-926437  0.389
2006 Grondal C, Enders D. Direct asymmetric organocatalytic de novo synthesis of carbohydrates Tetrahedron. 62: 329-337. DOI: 10.1016/j.tet.2005.09.060  0.38
2006 Enders D, Kirchhoff J, Lausberg V. Diastereo- and Enantioselective Synthesis of Lignan Building Blocks by Tandem Michael Addition/Electrophilic Substitution of Lithiated α-Amino Nitriles to Furan-2(5H)-one Liebigs Annalen. 1996: 1361-1366. DOI: 10.1002/jlac.199619960904  0.379
2006 Enders D, Knopp M, Runsink J, Raabe G. The First Asymmetric Carroll Rearrangement Diastereo- and Enantioselective Synthesis of Polyfunctional Ketones with Vicinal Quaternary and Tertiary Stereogenic Centers Liebigs Annalen. 1996: 1095-1116. DOI: 10.1002/jlac.199619960708  0.47
2006 Enders D, Meyer O. Diastereo- and Enantioselective Diels-Alder Reactions of 2-Amino-1,3-dienes Liebigs Annalen. 1996: 1023-1035. DOI: 10.1002/jlac.199619960702  0.377
2006 Enders D, Lohray BB, Burkamp F, Bhushan V, Hett R. Regio- and Enantioselective Synthesis of α-Silyl Aldehydes and Ketones via SAMP/RAMP Hydrazones Liebigs Annalen. 1996: 189-200. DOI: 10.1002/jlac.199619960207  0.417
2006 Enders D, Reinhold U. Diastereo- and Enantioselective Synthesis of 1,2-Amino Alcohols and Protected α-Hydroxy Aldehydes from Glycol Aldehyde Hydrazones Liebigs Annalen. 1996: 11-26. DOI: 10.1002/Jlac.199619960104  0.406
2006 Enders D, Chow S. Organocatalytic asymmetric Michael addition of 2,2-dimethyl-1,3-dioxan-5- one to nitro alkenes employing proline-based catalysts European Journal of Organic Chemistry. 4578-4584. DOI: 10.1002/Ejoc.200600464  0.383
2006 Enders D, Moll A, Bats JW. Asymmetric synthesis of-3-substituted γ- and δ-sultams European Journal of Organic Chemistry. 1271-1284. DOI: 10.1002/ejoc.200500860  0.424
2006 Enders D, Saint-Dizier A, Lannou MI, Lenzen A. The phospha-Michael addition in organic synthesis European Journal of Organic Chemistry. 29-49. DOI: 10.1002/Ejoc.200500593  0.456
2006 Enders D, Niemeier O, Balensiefer T. Cover Picture: Asymmetric Intramolecular Crossed-Benzoin Reactions by N-Heterocyclic Carbene Catalysis (Angew. Chem. Int. Ed. 9/2006) Angewandte Chemie International Edition. 45: 1327-1327. DOI: 10.1002/Anie.200690029  0.443
2006 Enders D, Niemeier O, Balensiefer T. Titelbild: Asymmetric Intramolecular Crossed-Benzoin Reactions by N-Heterocyclic Carbene Catalysis (Angew. Chem. 9/2006) Angewandte Chemie. 118: 1351-1351. DOI: 10.1002/Ange.200690029  0.451
2005 Enders D, Lenzen A, Backes M, Janeck C, Catlin K, Lannou MI, Runsink J, Raabe G. Asymmetric total synthesis of the 1-epi-aglycon of the cripowellins A and B. The Journal of Organic Chemistry. 70: 10538-51. PMID 16323869 DOI: 10.1021/Jo0518093  0.534
2005 Boudou M, Enders D. Asymmetric synthesis of tetrahydropalmatine via tandem 1,2-addition/cyclization. The Journal of Organic Chemistry. 70: 9486-94. PMID 16268624 DOI: 10.1021/Jo051554T  0.555
2005 Enders D, Grondal C, Vrettou M, Raabe G. Asymmetric synthesis of selectively protected amino sugars and derivatives by a direct organocatalytic Mannich reaction. Angewandte Chemie (International Ed. in English). 44: 4079-83. PMID 15924286 DOI: 10.1002/anie.200500810  0.43
2005 Enders D, Lenzen A, Raabe G. Asymmetric synthesis of the 1-epi aglycon of the cripowellins A and B. Angewandte Chemie (International Ed. in English). 44: 3766-9. PMID 15892131 DOI: 10.1002/Anie.200500556  0.539
2005 Enders D, Voith M, Lenzen A. The dihydroxyacetone unit--a versatile C(3) building block in organic synthesis. Angewandte Chemie (International Ed. in English). 44: 1304-25. PMID 15651077 DOI: 10.1002/Anie.200400659  0.487
2005 Enders D, Grondal C. Direct organocatalytic de novo synthesis of carbohydrates. Angewandte Chemie (International Ed. in English). 44: 1210-2. PMID 15651015 DOI: 10.1002/anie.200462428  0.341
2005 Enders D, Niemeier O. Asymmetric Synthesis of β-Substituted γ-Lactams Employing the SAMP-/RAMP-Hydrazone Methodology. Application to the Synthesis of (R)-(-)-Baclofen Heterocycles. 66: 385. DOI: 10.3987/Com-05-S(K)41  0.516
2005 Enders D, Lenzen A, Raabe G. Synthesis of 1-epi-Cripowellin A and B Aglycone Synfacts. 2006: 0005-0005. DOI: 10.1055/S-2005-921658  0.338
2005 Enders D, Gries J. Asymmetric Synthesis of Substituted Azetidine Type α- and β-Amino Acids Synthesis. 2005: 3508-3516. DOI: 10.1055/S-2005-918421  0.455
2005 Enders D, Noll S, Bats JW. Efficient entry to diastereo- and enantiomerically pure α-branched [2.2] paracyclophanyl-alkylamines Synlett. 2005: 2679-2681. DOI: 10.1055/S-2005-917095  0.476
2005 Enders D, Hüttl MRM. Direct organocatalytic α-fluorination of aldehydes and ketones Synlett. 2005: 991-993. DOI: 10.1055/S-2005-864813  0.43
2005 Deniau E, Enders D, Couture A, Grandclaudon P. Asymmetric synthesis of 3-hetero-substituted 2,3-dihydro-1H-isoindol-1-ones Tetrahedron: Asymmetry. 16: 875-881. DOI: 10.1016/J.Tetasy.2005.01.012  0.472
2005 Enders D, Breuer I, Nühring A. First asymmetric synthesis of (+)-sordidin and (-)-7-epi-sordidin, aggregation pheromones of the banana weevil Cosmopolites sordidus European Journal of Organic Chemistry. 2005: 2677-2683. DOI: 10.1002/Ejoc.200500112  0.439
2005 Enders D, Milovanovic M, Voloshina E, Raabe G, Fleischhauer J. First asymmetric synthesis and determination of the absolute configuration of a lignan isolated from virola sebifera European Journal of Organic Chemistry. 1984-1990. DOI: 10.1002/Ejoc.200400885  0.467
2005 Enders D, Vignola N, Berner OM, Harnying W. Efficient Asymmetric Synthesis of α-Alkylated Benzylic Methyl Sulfonates. Cheminform. 36. DOI: 10.1002/chin.200532102  0.352
2005 Enders D, Grondal C, Vrettou M, Raabe G. Asymmetrische Synthese von selektiv geschützten Aminozuckern und ihren Derivaten über direkte organokatalytische Mannich‐Reaktion Angewandte Chemie. 117: 4147-4151. DOI: 10.1002/Ange.200500810  0.387
2004 Enders D, Balensiefer T. Nucleophilic carbenes in asymmetric organocatalysis. Accounts of Chemical Research. 37: 534-41. PMID 15311952 DOI: 10.1021/ar030050j  0.441
2004 Enders D, Nühring A, Runsink J. Efficient asymmetric synthesis of alpha-alkylated 1, 4-cyclohexanedione derivatives, important chiral building blocks in the synthesis of natural products. Chirality. 12: 374-7. PMID 10824155 DOI: 10.1002/(Sici)1520-636X(2000)12:5/6<374::Aid-Chir13>3.0.Co;2-G  0.49
2004 Enders D, Backes M. Asymmetric synthesis of alpha,gamma-substituted gamma-alkoxy methyl sulfonates via diastereospecific ring-opening of sultones Arkivoc. 2004. DOI: 10.3998/Ark.5550190.0005.212  0.358
2004 Enders D, Signore GD. Asymmetric Synthesis of Heterocyclic β-Aminosulfones via Nucleophilic 1,2-Addition of 2-Lithiobenzo[b]thiophene to Aldehyde-SAMP-hydrazones Heterocycles. 64: 101-120. DOI: 10.3987/Com-04-S(P)3  0.487
2004 Enders D, Wortmann L, Raabe G, Dücker B. A Highly Flexible Route to 1,2,3,4,5,6- Hexahydro-5-hydroxypyrimidin-2-ones as Potential HIV Protease Inhibitors Heterocycles. 62: 559. DOI: 10.3987/Com-03-S(P)51  0.411
2004 Enders D, Moser M, Geibel G, Laufer MC. Diastereo- and enantioselective synthesis of differently N, O-protected 1,3-amino alcohols with three neighbouring stereogenic centers Synthesis. 2004: 2040-2046. DOI: 10.1055/S-2004-829142  0.443
2004 Enders D, Lenzen A, Müller M. Efficient Asymmetric Syntheses of (+)-Strictifolione Synthesis. 2004: 1486-1496. DOI: 10.1055/S-2004-822387  0.5
2004 Enders D, Rijksen C, Bremus-Köbberling E, Gillner A, Köbberling J. A triazene-based new photolabile linker in solid phase chemistry Tetrahedron Letters. 45: 2839-2841. DOI: 10.1016/J.Tetlet.2004.02.002  0.302
2004 Enders D, Backes M. First asymmetric synthesis of both enantiomers of Tropional® and their olfactory evaluation Tetrahedron: Asymmetry. 15: 1813-1817. DOI: 10.1016/J.Tetasy.2004.04.026  0.455
2004 Enders D, Gries J, Kim ZS. Asymmetric synthesis of 2-mono- and 2,3-trans-disubstituted azetidines European Journal of Organic Chemistry. 4471-4482. DOI: 10.1002/ejoc.200400473  0.44
2004 Enders D, Müller‐Hüwen A. Asymmetric Synthesis of 2‐Amino‐1,3‐diols and D‐erythro‐Sphinganine European Journal of Organic Chemistry. 2004: 1732-1739. DOI: 10.1002/Ejoc.200300788  0.448
2004 Couture A, Deniau E, Enders D, Grandclaudon P. New Approach to the Synthesis of Chiral 3-Substituted Isoindolinones Cheminform. 35. DOI: 10.1002/chin.200411236  0.349
2003 Enders D, Del Signore G, Berner OM. First asymmetric synthesis of (-)-lintetralin via intramolecular Friedel-Crafts-type cyclization. Chirality. 15: 510-3. PMID 12774291 DOI: 10.1002/Chir.10242  0.559
2003 Lassaletta JM, Vázquez J, Prieto A, Fernández R, Raabe G, Enders D. Asymmetric synthesis of succinic semialdehyde derivatives. The Journal of Organic Chemistry. 68: 2698-703. PMID 12662040 DOI: 10.1021/Jo026557+  0.484
2003 Vignola N, Dahmen S, Enders D, Bräse S. Efficient synthesis of sulfonic, phosphoric, and phosphinic esters employing alkylating polymer-bound reagents. Journal of Combinatorial Chemistry. 5: 138-44. PMID 12625703 DOI: 10.1021/Cc0200787  0.571
2003 Enders D, Burkamp F. α-Heterosubstituted aldehydes in organic synthesis. Enantioselective approaches to new analogues of mevinic acids Collection of Czechoslovak Chemical Communications. 68: 975-1006. DOI: 10.1135/Cccc20030975  0.54
2003 Enders D, Wallert S, Runsink J. Asymmetric Synthesis of β-AminoCyclohexyl Sulfonates, β-Sultams and γ-Sultones Synthesis. 2003: 1856-1868. DOI: 10.1055/S-2003-41029  0.449
2003 Enders D, Klumpen T, Raabe G. Asymmetric Synthesis of Planar Chiral 2-Monosubstituted Diferrocenyl Ketones Synlett. 2003: 1198-1200. DOI: 10.1055/S-2003-39897  0.51
2003 Deniau E, Enders D, Couture A, Grandclaudon P. A new synthetic route to highly enantioenriched 3-substituted-2,3-dihydro-1H-isoindol-1-ones Tetrahedron: Asymmetry. 14: 2253-2258. DOI: 10.1016/S0957-4166(03)00409-9  0.482
2003 Enders D, Steinbusch D. An Efficient Asymmetric Synthesis of Tarchonanthuslactone European Journal of Organic Chemistry. 2003: 4450-4454. DOI: 10.1002/Ejoc.200300412  0.53
2003 Enders D, Harnying W, Vignola N. Asymmetric Synthesis ofα,γ-Substitutedγ-Sultones via Allylation of Chiral Lithiated Sulfonates European Journal of Organic Chemistry. 2003: 3939-3947. DOI: 10.1002/ejoc.200300342  0.42
2003 Enders D, Moll A, Schaadt A, Raabe G, Runsink J. A Flexible Asymmetric Synthesis ofanti-1,2-Sulfanyl Amines European Journal of Organic Chemistry. 2003: 3923-3938. DOI: 10.1002/ejoc.200300249  0.431
2003 Enders D, Jandeleit B, Berg Sv. (+)‐(1R,2S,3R)‐Tetracarbonyl[(1–3η)‐1‐(Phenylsulfonyl)‐ But‐2‐en‐1‐yl]Iron(1+) Tetrafluoroborate Organic Syntheses. 189-189. DOI: 10.1002/0471264180.Os078.21  0.318
2003 Enders D, Berg Sv, Jandeleit B. Synthesis of (−)‐(E,S)‐3‐(Benzyloxy)‐1‐Butenyl Phenyl Sulfone Via a Horner‐Wadsworth‐Emmons Reaction of (−)‐(S)‐2‐(Benzyloxy)Propanal Organic Syntheses. 177-177. DOI: 10.1002/0471264180.Os078.20  0.407
2003 Enders D, Berg Sv, Jandeleit B. Diethyl [(Phenylsulfonyl)Methyl]Phosphonate Organic Syntheses. 169-169. DOI: 10.1002/0471264180.Os078.19  0.319
2003 Enders D, Kipphardt H, Fey P. Asymmetric Syntheses Using the SAMP‐/RAMP‐Hydrazone Method: (S)‐(+)‐4‐Methyl‐3‐Heptanone Organic Syntheses. 183-183. DOI: 10.1002/0471264180.Os065.24  0.346
2003 Enders D, Fey P, Kipphardt H. (S)‐(−)‐1‐Amino‐2‐Methoxymethylpyrrolidine (SAMP) and (R)‐(+)‐1‐Amino‐2‐Methoxymethylpyrrolidine (RAMP), Versatile Chiral Auxiliaries Organic Syntheses. 173-173. DOI: 10.1002/0471264180.Os065.23  0.383
2002 Enders D, Vicario JL, Job A, Wolberg M, Müller M. Asymmetric total synthesis of (-)-callystatin A and (-)-20-epi-callystatin A employing chemical and biological methods. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 4272-84. PMID 12298019 DOI: 10.1002/1521-3765(20020916)8:18<4272::Aid-Chem4272>3.0.Co;2-K  0.552
2002 Vázquez J, Prieto A, Fernández R, Enders D, Lassaletta JM. Asymmetric Michael addition of formaldehyde N,N-dialkylhydrazones to alkylidene malonates. Chemical Communications (Cambridge, England). 498-9. PMID 12120559 DOI: 10.1039/B200209B  0.389
2002 Vicario JL, Job A, Wolberg M, Müller M, Enders D. Asymmetric total synthesis of (-)-callystatin A employing the SAMP/RAMP hydrazone alkylation methodology. Organic Letters. 4: 1023-6. PMID 11893212 DOI: 10.1021/Ol0256116  0.579
2002 Enders D, Adam J, Oberbörsch S, Ward D. Asymmetric Mannich reactions by α-silyl controlled aminomethylation of ketones Synthesis. 2002: 2737-2748. DOI: 10.1055/S-2002-35998  0.468
2002 Funabiki K, Nagamori M, Matsui M, Enders D. Asymmetric Synthesis of Both Enantiomers of α-Trifluoromethyl Substituted Homoallylamine Synthesis. 2002: 2585-2588. DOI: 10.1055/S-2002-35631  0.512
2002 Enders D, Meiers M. Diastereo- and Enantioselective Syntheses of C2-Symmetric 1,n-Diamines by Nucleophilic Addition to Dialdehyde-SAMP-Hydrazones Synthesis. 2002: 2542-2560. DOI: 10.1055/S-2002-35628  0.394
2002 Enders D, Schüßeler T. First Highly Efficient Asymmetric Synthesis of the Hyrtios Erectus Diketotriterpenoid Synthesis. 2002: 2280-2288. DOI: 10.1055/S-2002-34949  0.408
2002 Enders D, Voith M, Ince SJ. Preparation and Reactions of 2,2-Dimethyl-1,3-dioxan-5-one-SAMP-Hydrazone: A Versatile Chiral Dihydroxyacetone Equivalent Synthesis. 2002: 1775-1779. DOI: 10.1055/S-2002-33646  0.439
2002 Enders D, Voith M. Asymmetric Synthesis of Monoprotected Double Allylic Alcohols Synthesis. 2002: 1571-1577. DOI: 10.1055/S-2002-33341  0.469
2002 Enders D, Ince SJ, Bonnekessel M, Runsink J, Raabe G. Chiral Dihydroxyacetone Equivalents in Synthesis: Rapid Assembly of Styryl 1,2-Polyols as an Entry to the Styryllactone Family of Natural Products Synlett. 2002: 0962-0966. DOI: 10.1055/S-2002-31905  0.407
2002 Enders D, Oberbörsch S. Asymmetric Mannich reactions with α-silylated trimethylsilyl enol ethers and N-alkoxycarbonyl imines Synlett. 2002: 471-473. DOI: 10.1055/S-2002-20468  0.467
2002 Enders D, Wallert S. Asymmetric Synthesis of β-Amino-cyclohexyl Sulfonates via aza Michael Addition Synlett. 2002: 0304-0306. DOI: 10.1055/s-2002-19766  0.322
2002 Enders D, Kallfass U, Nolte B. A short diastereo- and enantioselective synthesis of cis-4,5-disubstituted oxazolidin-2-ones Synlett. 2002: 33-36. DOI: 10.1055/S-2002-19341  0.536
2002 Enders D, Voith M. Asymmetric Synthesis of Pseudo C2-Symmetric 2-Methyl Substituted 1,3-Diols Synlett. 2002: 29-32. DOI: 10.1055/S-2002-19337  0.523
2002 Enders D, Nolte B, Runsink J. Asymmetric synthesis of 2-substituted piperidin-3-ols Tetrahedron Asymmetry. 13: 587-593. DOI: 10.1016/S0957-4166(02)00133-7  0.437
2002 Enders D, Nolte B, Raabe G, Runsink J. Asymmetric synthesis and structural assignment of (-)-α-conhydrine Tetrahedron Asymmetry. 13: 285-291. DOI: 10.1016/S0957-4166(02)00066-6  0.462
2002 Deniau E, Enders D. A new and versatile synthetic route to 2-dimethylamino-3-alkyl and arylmethylene-2,3-dihydro-1H-isoindol-1-ones Tetrahedron Letters. 43: 8055-8058. DOI: 10.1016/S0040-4039(02)01972-X  0.446
2002 Enders D, Schüßeler T. Asymmetric synthesis of all stereoisomers of 7,11-dimethylheptadecane and 7-methylheptadecane, the female pheromone components of the spring hemlock looper and the pitch pine looper Tetrahedron Letters. 43: 3467-3470. DOI: 10.1016/S0040-4039(02)00595-6  0.427
2002 Job A, Janeck CF, Bettray W, Peters R, Enders D. The SAMP-/RAMP-hydrazone methodology in asymmetric synthesis Tetrahedron. 58: 2253-2329. DOI: 10.1016/S0040-4020(02)00080-7  0.489
2002 Enders D, Thomas C, Vignola N, Raabe G. Asymmetric Synthesis of -Substituted N-Methylsulfonamides Helvetica Chimica Acta. 85: 3657-3677. DOI: 10.1002/1522-2675(200211)85:11<3657::AID-HLCA3657>3.0.CO;2-A  0.373
2002 Enders D, Kallfass U. Ein effizienter nucleophiler Carben‐Katalysator für die asymmetrische Benzoinkondensation Angewandte Chemie. 114: 1822-1824. DOI: 10.1002/1521-3757(20020517)114:10<1822::Aid-Ange1822>3.0.Co;2-W  0.42
2002 Enders D, Vignola N, Berner OM, Bats JW. Erste hoch effiziente asymmetrische Synthese vonα-substituierten Methylsulfonaten Angewandte Chemie. 114: 116-119. DOI: 10.1002/1521-3757(20020104)114:1<116::Aid-Ange116>3.0.Co;2-5  0.398
2002 Berner O, Tedeschi L, Enders D. Asymmetric Michael Additions to Nitroalkenes European Journal of Organic Chemistry. 2002: 1877. DOI: 10.1002/1099-0690(200206)2002:12<1877::AID-EJOC1877>3.0.CO;2-U  0.4
2001 Schunk S, Enders D. Solid-phase synthesis of beta-amino ketones and six-ring carbamates via immobilized alpha-alkoxycarbonylamino sulfones. Organic Letters. 3: 3177-80. PMID 11574024 DOI: 10.1021/Ol016487D  0.483
2001 Enders D, Funabiki K. Efficient asymmetric synthesis of alpha-trifluoromethyl-substituted primary amines via nucleophilic 1,2-addition to trifluoroacetaldehyde SAMP- or RAMP-hydrazone. Organic Letters. 3: 1575-7. PMID 11388870  0.391
2001 Enders D, Kirchhoff JH, Köbberling J, Peiffer TH. Asymmetric synthesis of alpha-branched primary amines on solid support via novel hydrazine resins. Organic Letters. 3: 1241-4. PMID 11348204 DOI: 10.1021/Ol015721X  0.492
2001 Kirchhoff JH, Bräse S, Enders D. A Novel Hydrazine Linker Resin and Its Application for the Solid-Phase Synthesis of alpha-Branched Primary Amines. Journal of Combinatorial Chemistry. 3: 71-77. PMID 11148066 DOI: 10.1021/Cc000062L  0.559
2001 Enders D, Thiebes C. Efficient stereoselective syntheses of piperidine, pyrrolidine, and indolizidine alkaloids Pure and Applied Chemistry. 73: 573-578. DOI: 10.1351/pac200173030573  0.466
2001 Enders D, Braig V, Raabe G. Asymmetric synthesis of 3-aryl-substituted 2,3-dihydro-1H-isoindol-1-ones Canadian Journal of Chemistry. 79: 1528-1535. DOI: 10.1139/v01-140  0.384
2001 Job A, Wolberg M, Müller M, Enders D. Asymmetric Synthesis of S-(+)-Argentilactone and S-(-)-Goniothalamin Synlett. 2001: 1796-1798. DOI: 10.1055/S-2001-18088  0.353
2001 Enders D, Nühring A, Runsink J, Raabe G. Asymmetric Synthesis of Protected 2-Keto-1,3-diol and 1,2,3-Triol Building Blocks Bearing a Quaternary Stereogenic Center Synthesis. 2001: 1406-1414. DOI: 10.1055/S-2001-15236  0.454
2001 Enders D, Jandeleit B, von Berg S, Raabe G, Runsink J. Iron-Mediated Allylic Substitution Reactions with Chirality Transfer. Stereochemistry of the Formation of Diastereo- and Enantiomerically Enriched Olefinic and Allylic Tetracarbonyl Iron Complexes Organometallics. 20: 4312-4332. DOI: 10.1021/Om010343L  0.37
2001 Vignola N, Dahmen S, Enders D, Bräse S. Synthesis of alkyl sulfonates from sulfonic acids or sodium sulfonates using solid-phase bound reagents Tetrahedron Letters. 42: 7833-7836. DOI: 10.1016/S0040-4039(01)01683-5  0.547
2001 Enders D, Klumpen T. Asymmetric synthesis of planar chiral 2-mono- and 2,2′-disubstituted 1,1′-bisbenzoylferrocenes Journal of Organometallic Chemistry. 637: 698-709. DOI: 10.1016/S0022-328X(01)00982-2  0.516
2001 Enders D, Gielen H. Synthesis of chiral triazolinylidene and imidazolinylidene transition metal complexes and first application in asymmetric catalysis Journal of Organometallic Chemistry. 617: 70-80. DOI: 10.1016/S0022-328X(00)00600-8  0.363
2001 Enders D, Nguyen D. ChemInform Abstract: Synthesis of Enantioenriched Substituted Tetrahydrofurans and Tetrahydropyrans via Iron-Mediated Chirality Transfer and Ring Closure. Cheminform. 32: no-no. DOI: 10.1002/chin.200117109  0.305
2000 Enders D, Geibel G, Osborne S. Diastereo- and enantioselective total synthesis of stigmatellin A. Chemistry (Weinheim An Der Bergstrasse, Germany). 6: 1302-9. PMID 10840951 DOI: 10.1002/(Sici)1521-3765(20000417)6:8<1302::Aid-Chem1302>3.0.Co;2-J  0.492
2000 Schunk S, Enders D. Solid-phase synthesis of beta-lactams via the ester enolate-imine condensation route. Organic Letters. 2: 907-10. PMID 10768183 DOI: 10.1021/Ol0055465  0.404
2000 Enders D, Wortmann L, Peters R. Recovery of carbonyl compounds from N,N-dialkylhydrazones. Accounts of Chemical Research. 33: 157-69. PMID 10727205 DOI: 10.1021/ar990062y  0.306
2000 Enders D, Teschner P, Raabe G. Diastereo- and Enantioselective Synthesis of g- and d-Lactams Bearing a Propionic Acid a-Side-Chain via Michael Addition of N-Dialkylamino Lactams to Enoates Heterocycles. 52: 733-749. DOI: 10.3987/Com-99-S83  0.386
2000 Job A, Nagelsdiek R, Enders D. Versatile Enantioselective Synthesis of Four Diastereomers of Serricornin, a Sex Pheromone of the Cigarette Beetle, Using the SAMP/RAMP-Hydrazone Method Collection of Czechoslovak Chemical Communications. 65: 524-538. DOI: 10.1135/Cccc20000524  0.407
2000 Enders D, Oberbörsch S, Adam J. α-Silyl Controlled Asymmetric Mannich Reactions of Acyclic Ketones with Imines Synlett. 2000: 644-646. DOI: 10.1055/S-2000-6595  0.386
2000 Enders D, Peters R, Lochtman R, Runsink J. Enantioselective Synthesis of Planar Chiralortho-Functionalized Ferrocenyl Ketones European Journal of Organic Chemistry. 2000: 2839-2850. DOI: 10.1055/S-1997-1047  0.489
2000 Enders D, Peters R, Lochtman R, Runsink J. Enantioselective Synthesis of Planar Chiral ortho-Functionalised Ferrocenylketones Synlett. 12: 1462-1464. DOI: 10.1055/s-1997-1047  0.417
2000 Enders D, Schüßeler T. First asymmetric synthesis of 6-methyl-3-nonanone, the female-produced sex pheromone of the caddisfly Hesperophylax occidentalis New Journal of Chemistry. 24: 973-975. DOI: 10.1039/B006832M  0.43
2000 Enders D, Ullrich EC. Asymmetric pinacol coupling of aromatic aldehydes with TiCl2/enantiopure amine or hydrazine reagents Tetrahedron-Asymmetry. 11: 3861-3865. DOI: 10.1016/S0957-4166(00)00379-7  0.479
2000 Enders D, Thiebes C. ChemInform Abstract: Enantioselective Synthesis of Both Enantiomers of Bgugaine Employing the SAMP-Hydrazone Method. Cheminform. 31: no-no. DOI: 10.1002/chin.200040207  0.366
2000 Enders D, Tedeschi L, Bats JW. Asymmetrische Syntheseα-substituierterβ-Nitrophosphonsäuren durch phospha-analoge Michael-Addition an aromatische Nitroalkene Angewandte Chemie. 112: 4774-4776. DOI: 10.1002/1521-3757(20001215)112:24<4774::Aid-Ange4774>3.0.Co;2-T  0.426
2000 Enders D, Müller S, Raabe G, Runsink J. Asymmetric Synthesis of α-Substituted β-Amino Sulfones by Aza-Michael Addition to Alkenyl Sulfones and Subsequent α-Alkylation European Journal of Organic Chemistry. 2000: 879-892. DOI: 10.1002/(Sici)1099-0690(200003)2000:6<879::Aid-Ejoc879>3.0.Co;2-E  0.474
1999 Enders D, Meyer I, Runsink J, Raabe G. Diastereo- And Enantioselective Synthesis Of Delta 2-1,2,4-Oxadiazolines By 1,3-Dipolar Cycloaddition Of Nitrile Oxides With Chiral Hydrazones Heterocycles. 50: 995-1024. DOI: 10.3987/Com-98-S(H)100  0.46
1999 Teles JH, Breuer K, Enders D, Gielen H. One Pot Synthesis Of 3,4-Disubstituted 1-Alkyl-4H-1,2,4-Triazol-1-Ium Salts Synthetic Communications. 29: 1-9. DOI: 10.1080/00397919908085727  0.418
1999 Enders D, Müller SF, Raabe G. Asymmetric Synthesis of α-Substituted β-Amino Sulfones by aza-Michael Addition / α-Alkylation Synlett. 6: 741-743. DOI: 10.1055/S-1999-972952  0.429
1999 Enders D, Klein D. A Novel Enantioselective Synthesis of α-Azido Ketones Synlett. 6: 719-720. DOI: 10.1055/S-1999-933097  0.491
1999 Enders D, Teschner P, Gröbner R, Raabe G. Asymmetric Michael Additions via 6- and 7-Membered Lactone SAMP-Hydrazones: Diastereo- and Enantioselective Synthesis of Substituted Lactone Esters Synthesis. 1999: 237-242. DOI: 10.1055/S-1999-3397  0.567
1999 Lazny R, Poplawski J, Köbberling J, Enders D, Bräse S. Triazenes: A Useful Protecting Strategy for Sensitive Secondary Amines Synlett. 1999: 1304-1306. DOI: 10.1055/S-1999-2803  0.515
1999 Enders D, Otten T. α-Silyl Controlled Asymmetric Michael Additions of Acyclic and Cyclic Ketones to Nitroalkenes Synlett. 6: 747-749. DOI: 10.1055/S-1999-2715  0.416
1999 Enders D, Vázquez J. Asymmetric Synthesis of α-Substituted β-Formyl δ-Lactones via a Michael Addition/α-Alkylation Protocol Synlett. 1999: 629-631. DOI: 10.1055/S-1999-2665  0.426
1999 Enders D, Amaya AS, Pierre F. Conversion of aldehydes to amides via dimethyl sulfoxide oxidation of the corresponding α-aminonitriles New Journal of Chemistry. 23: 261-262. DOI: 10.1039/A809770D  0.442
1999 Enders D, Peters R, Runsink aJ, Bats JW. Novel Ferrocenyl Ligands with Planar and Central Chirality in Pd-Catalyzed Allylic Substitutions Organic Letters. 1: 1863-1866. DOI: 10.1021/Ol991139L  0.368
1999 Enders D, Thomas CR, Runsink J. 5-Amino-4-aryl-2,2-dimethyl-1,3-dioxans: application as chiral NMR shift reagents and derivatizing agents for acidic compounds Tetrahedron: Asymmetry. 10: 323-326. DOI: 10.1016/S0957-4166(99)00003-8  0.391
1999 Enders D, Hundertmark T. Iterative asymmetric synthesis of protected anti-1,3-polyols Tetrahedron Letters. 40: 4169-4172. DOI: 10.1016/S0040-4039(99)00645-0  0.504
1999 Bräse S, Köbberling J, Enders D, Lazny R, Wang M, Brandtner S. Triazenes as robust and simple linkers for amines in solid-phase organic synthesis Tetrahedron Letters. 40: 2105-2108. DOI: 10.1016/S0040-4039(99)00160-4  0.609
1999 Enders D, Wortmann L, Dücker B, Raabe G. Asymmetric Synthesis of 1,2,3,4,5,6‐Hexahydro‐5‐hydroxypyrimidin‐2‐ones as Potential HIV‐Protease Inhibitors Helvetica Chimica Acta. 82: 1195-1201. DOI: 10.1002/(Sici)1522-2675(19990804)82:8<1195::Aid-Hlca1195>3.0.Co;2-N  0.385
1999 Enders D, Müller SF, Raabe G. Enantioselective Synthesis ofβ-Amino Sulfones by aza-Michael Addition to Alkenyl Sulfones Angewandte Chemie International Edition. 38: 195-197. DOI: 10.1002/(Sici)1521-3773(19990115)38:1/2<195::Aid-Anie195>3.0.Co;2-6  0.468
1999 Enders D, Peters R, Lochtman R, Raabe G. Asymmetrische Synthese neuer planar- und zentral-chiraler Ferrocenylliganden Angewandte Chemie. 111: 2579-2581. DOI: 10.1002/(Sici)1521-3757(19990816)111:16<2579::Aid-Ange2579>3.0.Co;2-B  0.326
1999 Enders D, Müller SF, Raabe G. Enantioselektive Synthese von β-Aminosulfonen über azaanaloge Michael-Addition an Alkenylsulfone Angewandte Chemie. 111: 212-214. DOI: 10.1002/(Sici)1521-3757(19990115)111:1/2<212::Aid-Ange212>3.0.Co;2-E  0.355
1999 Enders D, Hundertmark T. Asymmetric Synthesis of (+)- and (–)-Streptenol A European Journal of Organic Chemistry. 1999: 751-756. DOI: 10.1002/(SICI)1099-0690(199904)1999:4<751::AID-EJOC751>3.0.CO;2-R  0.356
1998 Enders D, Kroll M, Raabe G, Runsink J. Diastereoselective Synthesis of Highly Substituted Five-Membered-Ring Oxygen Heterocycles by Zirconocene-Mediated C-C Coupling Reactions. Angewandte Chemie (International Ed. in English). 37: 1673-1675. PMID 29711525 DOI: 10.1002/(SICI)1521-3773(19980703)37:12<1673::AID-ANIE1673>3.0.CO;2-A  0.379
1998 Bräse S, Enders D, Köbberling J, Avemaria F. A Surprising Solid-Phase Effect: Development of a Recyclable "Traceless" Linker System for Reactions on Solid Support. Angewandte Chemie (International Ed. in English). 37: 3413-3415. PMID 29711298 DOI: 10.1002/(Sici)1521-3773(19981231)37:24<3413::Aid-Anie3413>3.0.Co;2-K  0.572
1998 Enders D, Lochtman R, Meiers M, Müller S, Lazny R. Efficient N-N Bond Cleavage of Chiral Trisubstituted Hydrazines with BH3 ⋅ THF Synlett. 1998: 1182-1184. DOI: 10.1055/S-1998-5742  0.349
1998 Enders D, Hett R. Asymmetric Synthesis of α′-Silylated α,β-Epoxy Ketones via Darzens Reaction Synlett. 1998: 961-962. DOI: 10.1055/s-1998-1832  0.372
1998 Enders D, Müller P, Klein D. Diastereo- and Enantioselective Synthesis of syn-2,3-Disubstituted 1,4-Diketones via Oxidative Coupling of Metalated Hydrazones Synlett. 1998: 43-44. DOI: 10.1055/S-1998-1562  0.36
1998 Enders D, Kramps L, Zhu J. Zinc-mediated asymmetric epoxidation of nitro alkenes with oxygen Tetrahedron: Asymmetry. 9: 3959-3962. DOI: 10.1016/S0957-4166(98)00424-8  0.429
1998 Enders D, Poiesz C, Joseph R. Enantioselective synthesis of protected α-aminoketones via electrophilic amination of α-silylketones with an oxaziridine Tetrahedron-Asymmetry. 9: 3709-3716. DOI: 10.1016/S0957-4166(98)00382-6  0.439
1998 Enders D, Maaßen R, Runsink J. First asymmetric nucleophilic displacement reactions on chiral α-substituted aldehyde hydrazones Tetrahedron: Asymmetry. 9: 2155-2180. DOI: 10.1016/S0957-4166(98)00205-5  0.534
1998 Enders D, Schäfer T, Mies W. Enantioselective synthesis of α-sulfenylated ketones and aldehydes via α-thiolation of metalated SAMP/RAMP hydrazones Tetrahedron. 54: 10239-10252. DOI: 10.1016/S0040-4020(98)00481-5  0.432
1998 Enders D, Kroll M, Raabe G, Runsink J. Zirconocene Mediated Diastereo- and Enantioselective Synthesis of 4,5,5-Trisubstituted 2-Alkoxytetrahydrofurans Molecules Online. 2: 109-113. DOI: 10.1007/S007830050065  0.491
1998 Enders D, Baus U, Müller P, Nicolaou KC, Jandeleit B. Asymmetric Synthesis of 3-Substituted 4-Oxoesters Using the SAMP-/RAMP-Hydrazone Method Molecules Online. 2: 15-21. DOI: 10.1007/S007830050049  0.606
1998 Enders D, Bolkenius M, V�zquez J, Lassaletta J, Fern�ndez R. Formaldehyde SAMP-Hydrazone - a neutral chiral formyl anion and cyanide equivalent Journal F�R Praktische Chemie/Chemiker-Zeitung. 340: 281-285. DOI: 10.1002/Prac.19983400315  0.372
1998 Enders D, Thomas CR, Raabe G, Runsink J. Enantioselektive Synthese von ?-substituiertenN-Methyl-sulfonamiden. Vorl�ufige Mitteilung Helvetica Chimica Acta. 81: 1329-1336. DOI: 10.1002/Hlca.19980810543  0.474
1998 Enders D, Dyker H, Leusink FR. Enantioselective Synthesis of Protected Isotetronic Acids Chemistry - a European Journal. 4: 311-320. DOI: 10.1002/(SICI)1521-3765(19980210)4:2<311::AID-CHEM311>3.0.CO;2-L  0.32
1998 Bräse S, Enders D, Köbberling J, Avemaria F. Ein überraschender Festphaseneffekt: Entwicklung eines regenerierbaren, „spurlosen” Linker-Systems für Festphasenreaktionen Angewandte Chemie. 110: 3614-3616. DOI: 10.1002/(Sici)1521-3757(19981217)110:24<3614::Aid-Ange3614>3.0.Co;2-R  0.42
1998 Enders D, Hundertmark T, Lampe C, Jegelka U, Scharfbillig I. Highly Diastereo- and Enantioselective Synthesis of Protectedanti-1,3-Diols European Journal of Organic Chemistry. 1998: 2839-2849. DOI: 10.1002/(sici)1099-0690(199812)1998:12<2839::aid-ejoc2839>3.0.co;2-7  0.453
1998 Enders D, Haertwig A, Runsink J. Diastereo- and Enantioselective Synthesis ofN-Protected 2-Amino 1,4-Diols by an Oxa Michael Addition/1,3-Dipolar Cycloaddition Protocol European Journal of Organic Chemistry. 1998: 1793-1802. DOI: 10.1002/(SICI)1099-0690(199809)1998:9<1793::AID-EJOC1793>3.0.CO;2-9  0.409
1998 Enders D, Lochtman R. Asymmetric Synthesis of (1-Ferrocenylalkyl)amine and 1,1′-Bis(1-aminoalkyl)ferrocene Derivatives European Journal of Organic Chemistry. 1998: 689-696. DOI: 10.1002/(Sici)1099-0690(199804)1998:4<689::Aid-Ejoc689>3.0.Co;2-S  0.52
1998 Enders D, Kirchhoff J, Gerdes P, Mannes D, Raabe G, Runsink J, Boche G, Marsch M, Ahlbrecht H, Sommer H. Structure and Reactivity of Lithiated α-Amino Nitriles European Journal of Organic Chemistry. 1998: 63-72. DOI: 10.1002/(Sici)1099-0690(199801)1998:1<63::Aid-Ejoc63>3.0.Co;2-H  0.322
1998 Enders D, Gielen H, Runsink J, Breuer K, Brode S, Boehn K. Diastereoselective Synthesis of Chiral (Triazolinylidene)rhodium Complexes Containing an Axis of Chirality European Journal of Inorganic Chemistry. 1998: 913-919. DOI: 10.1002/(Sici)1099-0682(199807)1998:7<913::Aid-Ejic913>3.0.Co;2-1  0.458
1997 Enders D, Jandeleit B, von Berg S. Synthesis of Highly Enantioenriched CompoundsviaIron Mediated Allylic Substitutions Synlett. 1997: 421-431. DOI: 10.1055/S-1997-6128  0.525
1997 Enders D, Kownatka D, Hundertmark T, Prokopenko OF, Runsink J. Asymmetric Michael Additions via 2,2-Dimethyl-1,3-dioxan-5-one SAMP-Hydrazone. Distereo- and Enantioselective Synthesis of Protected 3-Substituted 4,6-Dihydroxy-5-oxo Esters Synthesis. 1997: 649-652. DOI: 10.1055/S-1997-1397  0.56
1997 Enders D, Gielen H, Breuer K. Catalytic asymmetric hydrosilylation with (triazolinylidene)rhodium complexes containing an axis of chirality Tetrahedron: Asymmetry. 8: 3571-3574. DOI: 10.1016/S0957-4166(97)00519-3  0.421
1997 Enders D, Leriverend C. Diastereo- and enantioselective synthesis of protected vicinal silylamines via 1,2-addition to α-silyl-hydrazones Tetrahedron: Asymmetry. 8: 2787-2792. DOI: 10.1016/S0957-4166(97)00321-2  0.374
1997 Enders D, Reinhold U. Asymmetric synthesis of amines by nucleophilic 1,2-addition of organometallic reagents to the CN-double bond Tetrahedron: Asymmetry. 8: 1895-1946. DOI: 10.1016/S0957-4166(97)00208-5  0.455
1997 Enders D, Breuer K, Raabe G, Simonet J, Ghanimi A, Stegmann HB, Teles J. A stable carbene as π-acceptor electrochemical reduction to the radical anion Tetrahedron Letters. 38: 2833-2836. DOI: 10.1016/S0040-4039(97)00493-0  0.308
1997 Enders D, Wahl H, Papadopoulos K. Diastereo- and enantioselective synthesis of 2,3- and 1,2-disubstituted 4-oxophosphonates via asymmetric Michael addition Tetrahedron. 53: 12961-12978. DOI: 10.1016/S0040-4020(97)00814-4  0.471
1997 Enders D, Jandeleit B, von Berg S. “Chirality transfer” in iron-mediated dienylic substitutions via highly enantiomerically enriched planar chiral 1-phenylsulfonyl-substituted tricarbonyl(η5-pentadienyl) iron(1 +) complexes Journal of Organometallic Chemistry. 533: 219-236. DOI: 10.1016/S0022-328X(96)06850-7  0.386
1997 Demir AS, Enders D. Regioselective Alkylations of Cyclic 1,3-Diketonesvia Metalated Dimethylhydrazones Journal FüR Praktische Chemie/Chemiker-Zeitung. 339: 553-563. DOI: 10.1002/Prac.19973390199  0.344
1997 Enders D, Breuer K, Teles JH, Ebel K. 1,3,4‐Triphenyl‐4,5‐dihydro‐1H‐1,2,4‐triazol‐5‐ylidene – applications of a stable carbene in synthesis and catalysis Journal Fur Praktische Chemie-Chemiker-Zeitung. 339: 397-399. DOI: 10.1002/Prac.19973390170  0.436
1997 Enders D, Bartzen D. Diastereo- and Enantioselective Synthesis of 4,5,6-Trisubstituted and 6-Monosubstituted Piperidin-2-ones Liebigs Annalen. 1997: 1115-1123. DOI: 10.1002/jlac.199719970610  0.455
1997 Enders D, Nübling C, Schubert H. Asymmetric Synthesis of Primary Amines by Nucleophilic Addition of Alkyllithium Compounds to Aldehyde SAMP/RAMP Hydrazones Liebigs Annalen. 1997: 1089-1100. DOI: 10.1002/Jlac.199719970608  0.481
1997 Enders D, Kaiser A. Asymmetric Synthesis of (R,S)-Dehydroiridodial, (R,S)-Dehydroiridodiol and Analogues Liebigs Annalen. 1997: 485-493. DOI: 10.1002/Jlac.199719970308  0.376
1997 Enders D, Potthoff M, Raabe G, Runsink J. Regio- and Enantioselective Synthesis ofα-Fluoroketones by Electrophilic Fluorination ofα-Silylketone Enolates withN-Fluorobenzosulfonimide Angewandte Chemie International Edition in English. 36: 2362-2364. DOI: 10.1002/anie.199723621  0.465
1997 Enders D, Potthoff M, Raabe G, Runsink J. Regio- und enantioselektive Synthese von α-Fluorketonen via elektrophile Fluorierung von α-Silylketonenolaten mitN-Fluor-N,N-bis(phenylsulfonyl)amin Angewandte Chemie. 109: 2454-2456. DOI: 10.1002/Ange.19971092124  0.371
1996 Raabe G, Breuer K, Enders D, Teles JH. The Role of Conjugative Interaction in Stable Carbenes of the 1,2,4-Triazol-5-ylidene Type and their Energy of Dimerization. An Ab Initio Study Zeitschrift FüR Naturforschung A. 51: 95-101. DOI: 10.1515/Zna-1996-1-214  0.303
1996 Enders D, Bettray W. Recent advances in the development of highly enantioselective synthetic methods Pure and Applied Chemistry. 68: 569-580. DOI: 10.1351/Pac199668030569  0.489
1996 Enders D, Berg Sv, Jandeleit B. Iron-Mediated Allylic Substitutions with Complete Chirality Transfer. Synthesis of Functionalized γ-Substituted Alkenylsulfones of High Enantiomeric Purity Synlett. 1996: 18-20. DOI: 10.1055/S-1996-5313  0.447
1996 Enders D, Gröbner R, Raabe G, Runsink J. Enantioselective Synthesis of 2-Substituted 5-, 6- and 7-Membered Lactams via α-Alkylation of Their Chiral N-Dialkylamino Derivatives Synthesis. 1996: 941-948. DOI: 10.1055/S-1996-4443  0.531
1996 Enders D, Klatt M. Asymmetric Synthesis with (S)-2-Methoxymethylpyrrolidine (SMP) - a Pioneer Auxiliary Synthesis. 1996: 1403-1418. DOI: 10.1055/S-1996-4423  0.432
1996 Enders D, Schiffers R. Enantioselective Synthesis of Differently Protected 1,2-Diamines via α-Alkylation of Dibenzylaminoacetaldehyde SAMP-Hydrazone Synthesis. 1996: 53-58. DOI: 10.1055/S-1996-4166  0.484
1996 Enders D, Burkamp F, Runsink J. Diastereo- and enantio-selective synthesis of 6-heterosubstituted-3,5-dihydroxyesters: novel precursors of mevinolin analogues Chemical Communications. 609-610. DOI: 10.1039/Cc9960000609  0.483
1996 Enders D, Frank U, Fey P, Jandeleit B, Lohray BB. Synthesis of highly diastereo- and enantiomerically enriched tetracarbonyl(η3-allyl)iron(1+) complexes for allylic substitutions with silyl enol ethers and silyl ketene acetals Journal of Organometallic Chemistry. 519: 147-159. DOI: 10.1016/S0022-328X(96)06161-X  0.446
1996 Enders D, Knopp M. Novel asymmetric syntheses of (-)-malyngolide and (+)-epi-malyngolide Tetrahedron. 52: 5805-5818. DOI: 10.1016/0040-4020(96)00236-0  0.393
1996 Enders D, Hecker P, Meyer O. A novel approach to 2-amino-1,3-dienes by coupling of α-chloro enamines and alkenyl lithium compounds Tetrahedron. 52: 2909-2924. DOI: 10.1016/0040-4020(95)01126-9  0.487
1996 Enders D, Fey P, Schmitz T, Lohray BB, Jandeleit B. Regio- and stereoselective a4-umpolung reactions of α,β-unsaturated esters to 1,6-dicarbonyl compounds by addition of enantiopure nucleophiles to racemic tetracarbonyl (η3-alyl)iron(1+) complexes Journal of Organometallic Chemistry. 514: 227-232. DOI: 10.1016/0022-328X(95)06042-U  0.479
1996 Enders D, Breuer K, Runsink J, Henrique Teles J. Chemical Reactions of the Stable Carbene 1,3,4-Triphenyl-4,5-dihydro-1H-1,2,4-triazol-5-ylidene Liebigs Annalen. 1996: 2019-2028. DOI: 10.1002/Jlac.199619961212  0.394
1996 Enders D, Maaßen R, Han S. New Efficient, Flexible and Regioselective Synthesis of 2,4-Di- and 2,3,4-Trialkylated an Arylated 1H-Pyrroles Liebigs Annalen. 1996: 1565-1574. DOI: 10.1002/Jlac.199619961011  0.447
1996 Enders D, Breuer K, Runsink J, Teles JH. The First Asymmetric IntramolecularStetter Reaction. Preliminary Communication Helvetica Chimica Acta. 79: 1899-1902. DOI: 10.1002/Hlca.19960790712  0.514
1996 Enders D, Breuer K, Teles JH. A Novel Asymmetric Benzoin Reaction Catalyzed by a Chiral Triazolium Salt. Preliminary communication Helvetica Chimica Acta. 79: 1217-1221. DOI: 10.1002/Hlca.19960790427  0.523
1996 Enders D, Berg T, Raabe G, Runsink J. Enantioselektive Synthese von ?-Phosphinoketonen. Vorl�ufige Mitteilung Helvetica Chimica Acta. 79: 118-122. DOI: 10.1002/Hlca.19960790112  0.466
1996 Henrique Teles J, Melder J, Ebel K, Schneider R, Gehrer E, Harder W, Brode S, Enders D, Breuer K, Raabe G. The Chemistry of Stable Carbenes. Part 2. Benzoin-type condensations of formaldehyde catalyzed by stable carbenes Helvetica Chimica Acta. 79: 61-83. DOI: 10.1002/Hlca.19960790108  0.42
1996 Enders D, Gielen H, Raabe G, Runsink J, Teles JH. Synthesis and Stereochemistry of the First Chiral (Imidazolinylidene)- and (Triazolinylidene)palladium(ii) Complexes Chemische Berichte. 129: 1483-1488. DOI: 10.1002/Cber.19961291213  0.4
1996 Enders D, Haertwig A, Raabe G, Runsink J. Enantioselective Synthesis of Vicinal Amino Alcohols by Oxa-Michael Addition of(−)-N-Formylnorephedrine to Nitroalkenes Angewandte Chemie International Edition in English. 35: 2388-2390. DOI: 10.1002/Anie.199623881  0.39
1996 Enders D, Meiers M. Diastereo- and Enantioselective Synthesis ofC2-Symmetric, Protected 1,n-Diamines from Dialdehydes Angewandte Chemie International Edition in English. 35: 2261-2263. DOI: 10.1002/Anie.199622611  0.461
1996 Enders D, Ward D, Adam J, Raabe G. Efficient Regio- and Enantioselective Mannich Reactions Angewandte Chemie International Edition in English. 35: 981-984. DOI: 10.1002/Anie.199609811  0.474
1996 Enders D, Haertwig A, Raabe G, Runsink J. Enantioselektive Synthese von vicinalen Aminoalkoholen durch Oxa-Michael-Addition Angewandte Chemie. 108: 2540-2542. DOI: 10.1002/Ange.19961082026  0.478
1996 Enders D, Ward D, Adam J, Raabe G. Effiziente regio- und enantioselektive Mannich-Reaktionen Angewandte Chemie. 108: 1059-1062. DOI: 10.1002/Ange.19961080910  0.424
1995 Enders D, Backhaus D. Diastereo- and Enantioselective Synthesis of β-Substituted γ,δ-Unsaturated α-Hydroxy-Ketones via [2,3]-Wittig Rearrangement of α-Allyloxyketone-Hydrazones Synlett. 1995: 631-633. DOI: 10.1055/S-1995-5013  0.419
1995 Enders D, Gröbner R, Runsink J. Enantioselective Synthesis of 2-Substituted 6- and 7-Membered Lactones via α-Alkylation of Lactone Hydrazones Synthesis. 1995: 947-951. DOI: 10.1055/S-1995-4431  0.522
1995 Enders D, Man S, Maaβen R. New efficient and flexible synthesis of polysubstituted pyrroles Tetrahedron Letters. 36: 8007-8010. DOI: 10.1016/0040-4039(95)01717-V  0.405
1995 Enders D, Plant A, Backhaus D, Reinhold U. Asymmetric synthesis of α-substituted nitriles and cyanohydrins by oxidative cleavage of chiral aldehyde hydrazones with magnesium monoperoxyphthalate Tetrahedron. 51: 10699-10714. DOI: 10.1016/0040-4020(95)00647-Q  0.391
1995 Enders D, Jandeleit B, Prokopenko OF. Convergent synthesis of (R,R)-6,12-dimethylpentadecan-2-one, the female sex pheromone of the banded cucumber beetle by iron mediated chirality transfer Tetrahedron. 51: 6273-6284. DOI: 10.1016/0040-4020(95)00282-D  0.346
1995 Enders D, Prokopenko OF. Diastereo- and enantioselective synthesis of the 18-membered lichen macrolide (+)-aspicilin Liebigs Annalen. 1995: 1185-1191. DOI: 10.1002/jlac.1995199507161  0.406
1995 Enders D, Wahl H, Papadopoulos K. Asymmetric michael additions via SAMP/RAMP hydrazones enantioselective synthesis of 2‐substituted 4‐oxophosphonates Liebigs Annalen. 1995: 1177-1184. DOI: 10.1002/Jlac.1995199507160  0.5
1995 Enders D, Jandeleit B. Efficient and convergent synthesis of (R)‐(−)‐10‐methyltridecan‐2‐one, the sex pheromone of the spotted cucumber beetle, by iron‐mediated chirality transfer Liebigs Annalen. 1995: 1173-1176. DOI: 10.1002/Jlac.1995199507159  0.421
1995 Enders D, Plant A, Drechsel K, Prokopenko OF. A convenient enantioselective synthesis of (R)-(−)-phoracantholide I, a component of the defensive secretion of the eucalypt longicornPhoracantha synonyma Liebigs Annalen. 1995: 1127-1128. DOI: 10.1002/Jlac.1995199506153  0.473
1995 Enders D, Schankat J. Enantioselektive Synthese von Allyl‐, Propargyl‐ und 4‐En‐2‐inyl‐aminen durch 1,2‐Addition von Organocer‐Reagenzien an chirale Aldimine Helvetica Chimica Acta. 78: 970-992. DOI: 10.1002/Hlca.19950780419  0.496
1995 Enders D, Whitehouse DL, Runsink J. Diastereo- and Enantioselective Synthesis ofL-threo- andD-erythro-Sphingosine Chemistry - a European Journal. 1: 382-388. DOI: 10.1002/Chem.19950010609  0.526
1995 Enders D, Knopp M, Runsink J, Raabe G. Diastereo‐ and Enantioselective Synthesis of Polyfunctional Ketones with Adjacent Quaternary and Tertiary Centers by Asymmetric Carroll Rearrangement Angewandte Chemie International Edition in English. 34: 2278-2280. DOI: 10.1002/Anie.199522781  0.498
1995 Enders D, Reinhold U. Diastereo- and Enantioselective Synthesis of 1,2-Amino Alcohols from Glycol Aldehyde Hydrazones; Asymmetric Synthesis of(R,R)-Statin Angewandte Chemie International Edition in English. 34: 1219-1222. DOI: 10.1002/Anie.199512191  0.386
1995 Enders D, Wahl H, Bettray W. Enantioselective Synthesis ofβ-Amino Acids: TMS-SAMP as a Chiral Ammonia Equivalent for the Aza Analogous Michael Addition toα,β-Unsaturated Esters Angewandte Chemie International Edition in English. 34: 455-457. DOI: 10.1002/Anie.199504551  0.463
1995 Enders D, Knopp M, Runsink J, Raabe G. Diastereo- und enantioselektive Synthese von polyfunktionellen Ketonen mit benachbarten quartären und tertiären Stereozentren durch asymmetrische Carroll-Umlagerung Angewandte Chemie. 107: 2442-2445. DOI: 10.1002/Ange.19951072021  0.373
1995 Enders D, Wahl H, Bettray W. Enantioselektive Synthese von β‐Aminosäuren – TMS‐SAMP als chirales Ammoniak‐Äquivalent in der azaanalogen Michael‐Addition an α,β‐ungesättigte Ester Angewandte Chemie. 107: 527-529. DOI: 10.1002/Ange.19951070427  0.383
1994 Enders D, Jandeleit B. Iron-Mediated Complete Chirality Transfer in Allylic Substitutions. Efficient Synthesis of (-)-(S)-Myoporone Synthesis. 1994: 1327-1330. DOI: 10.1055/S-1994-25689  0.414
1994 Enders D, Plant A. Enantioselective Synthesis of α-Substituted Nitriles by Oxidative Cleavage of Aldehyde SAMP-Hydrazones with Magnesium Monoperoxyphthalate Synlett. 1994: 1054-1056. DOI: 10.1055/S-1994-23083  0.472
1994 Enders D, Kempen H. Enantioselective Synthesis of Allylic Alcohols via Asymmetric [2,3]-Sigmatropic Meisenheimer Rearrangement Synlett. 1994: 969-971. DOI: 10.1055/S-1994-23068  0.385
1994 Enders D, Reinhold U. Enantioselective Synthesis of Protected α-Hydroxy AldehydesviaAlkylation of Metalated Chiral Hydrazones Synlett. 1994: 792-794. DOI: 10.1055/S-1994-23007  0.436
1994 Enders D, Schäfer T, Piva O, Zamponi A. Enantioselective synthesis of 2-sulfenylated aldehydes: Alkylation of sulfenylated acetaldehyde SAMP-hydrazones Tetrahedron. 50: 3349-3362. DOI: 10.1016/S0040-4020(01)87015-0  0.732
1994 Enders D, Zamponi A, Schäfer T, Nübling C, Eichenauer H, Demir AS, Raabe G. Enantioselective Synthesis of Polyfunctional Small Building Blocks with a Quaternary Stereogenic Center Chemische Berichte. 127: 1707-1721. DOI: 10.1002/Cber.19941270922  0.521
1994 Enders D, Backhaus D, Runsink J. [2,3] Sigmatropic Wittig Rearrangement of Chiral Allyloxyacetaldehyde Hydrazones in the Diastereo- and Enantioselective Synthesis of Protected,γ,δ-Unsaturatedα-Hydroxyaldehydes and Cyanohydrins Angewandte Chemie International Edition in English. 33: 2098-2100. DOI: 10.1002/anie.199420981  0.401
1994 Enders D, Jandeleit B, Raabe G. Iron-Promoted, Regio- and Stereoselective Allylic Substitutions for the Synthesis of Alkenyl Sulfones Substituted at C-3† Angewandte Chemie. 33: 1949-1951. DOI: 10.1002/Anie.199419491  0.417
1994 Enders D, Backhaus D, Runsink J. [2,3]-Sigmatrope Wittig-Umlagerung chiraler Allyloxyacetaldehyd-Hydrazone zur diastereo- und enantioselektiven Synthese von geschützten, γ,δ-ungesättigten α-Hydroxyaldehyden und Cyanhydrinen Angewandte Chemie. 106: 2167-2170. DOI: 10.1002/Ange.19941062017  0.4
1994 Enders D, Jandeleit B, Raabe G. Eisen-unterstützte, regio- und stereoselektive allylische Substitutionen zu 3-substituierten Alkenylsulfonen Angewandte Chemie. 106: 2033-2035. DOI: 10.1002/Ange.19941061914  0.332
1993 Lohray BB, Enders D. Enantioselective Siloxybutylation of Aldehydes and Ketones by Lewis Acid Mediated Ring Opening of Tetrahydrofuran with Lithiated Hydrazones Synthesis. 1993: 1092-1094. DOI: 10.1055/S-1993-26007  0.506
1993 Enders D, Finkam M. Iron mediated synthesis of 4-amino-enoates of high enantiomeric purity Synlett. 1993: 401-403. DOI: 10.1055/S-1993-22470  0.352
1993 Enders D, Klatt M, Funk R. Enantioselective synthesis of protected β-amino acetals and β-amino acids by 1,2-addition of RM/CeCl3 to 3,3-ethylenedioxypropanal-SAMP-hydrazone Synlett. 1993: 226-228. DOI: 10.1055/S-1993-22412  0.359
1993 Enders D, Tiebes J, Kimpe ND, Keppens M, Stevens C, Smagghe G, Betz O. Enantioselective synthesis and determination of the configuration of stenusine, the spreading agent of the beetle Stenus comma Journal of Organic Chemistry. 58: 4881-4884. DOI: 10.1021/Jo00070A024  0.499
1993 Bhushan V, Lohray BB, Enders D. Efficient enantioselective synthesis of allylsilanes by wittig olefination of α-silylaldehydes Tetrahedron Letters. 34: 5067-5070. DOI: 10.1016/S0040-4039(00)60677-9  0.379
1993 Enders D, Papadopoulos K, Herdtweck E. Asymmetric Michael additions via SAMP-/RAMP-hydrazones enantioselective synthesis of 2-substituted 4-oxosulfones Tetrahedron. 49: 1821-1830. DOI: 10.1016/S0040-4020(01)80538-X  0.513
1993 Enders D, Finkam M. First Synthesis of the Cytotoxic and Antifungal C14‐Amine (2S,3E,5Z)‐2‐Amino‐3,5,13‐tetradecatriene Isolated from the New Zealand Ascidian Pseudodistoma novaezelandiae European Journal of Organic Chemistry. 1993: 551-555. DOI: 10.1002/Jlac.199319930190  0.456
1993 Enders D, Tiebes J. A New Asymmetric Synthesis of both Enantiomers of Coniine by 1,2-Addition of RLi/YbCl3 to Aldehyde SAMP Hydrazones Liebigs Annalen Der Chemie. 1993: 173-177. DOI: 10.1002/Jlac.199319930131  0.546
1993 Enders D, Schankat J. Enantioselektive Synthese von Allyl- und Propargylaminen durch nucleophile 1,2-Addition an chirale Aldimine. Preliminary communication Helvetica Chimica Acta. 76: 402-406. DOI: 10.1002/Hlca.19930760123  0.505
1993 Enders D, Scherer HJ, Runsink J. Diastereo‐ und enantioselektive Synthese 1,2‐trans‐substituierter Cycloalkancarbonsäureester und Sulfone durch Michael‐initiierte Cyclisierungen via SAMP‐/RAMP‐Hydrazone[1,2] Chemische Berichte. 126: 1929-1944. DOI: 10.1002/Cber.19931260825  0.554
1993 Enders D, Heider K, Raabe G. Diastereo- and Enantioselective Synthesis of 2-Substituted 3-Trialkylstannylcyclohexanones by Michael Addition of Trialkylstannyllithium to Cyclohexenone SAMP Hydrazone Angewandte Chemie International Edition in English. 32: 598-601. DOI: 10.1002/Anie.199305981  0.56
1993 Enders D, Jegelka U, Dücker B. Diastereo- and Enantioselective Synthesis ofC2-Symmetrical HIV-1 Protease Inhibitors Angewandte Chemie International Edition in English. 32: 423-425. DOI: 10.1002/Anie.199304231  0.303
1993 Enders D, Dyker H, Raabe G. Enantioselective Aldol Reactions with a Phosphoenolpyruvate Equivalent: Asymmetric Synthesis of 4-Hydroxy-2-oxocarboxylic Acid Esters Angewandte Chemie International Edition in English. 32: 421-423. DOI: 10.1002/anie.199304211  0.449
1993 Enders D, Heider K, Raabe G. Diastereo- und enantioselektive Synthese von 2-substituierten 3-Trialkylstannylcyclohexanonen durch Michael-Addition von Trialkylstannyllithium an Cyclohexenon-SAMP-Hydrazon Angewandte Chemie. 105: 592-595. DOI: 10.1002/Ange.19931050419  0.461
1993 Enders D, Jegelka U, Dücker B. Diastereo‐ und enantioselektive Synthese C2‐symmetrischer HIV‐1‐Protease‐Inhibitoren Angewandte Chemie. 105: 423-425. DOI: 10.1002/Ange.19931050316  0.399
1993 Enders D, Dyker H, Raabe G. Enantioselektive Aldolreaktionen mit einem Phosphoenolpyruvat-Äquivalent: asymmetrische Synthese von 4-Hydroxy-2-oxocarbonsäureestern Angewandte Chemie. 105: 420-423. DOI: 10.1002/Ange.19931050315  0.443
1993 Enders D, Funk R, Klatt M, Raabe G, Hovestreydt ER. Enantioselektive Synthese von α‐Aminoacetalen und α‐Aminosäuren durch nucleophile 1,2‐Addition an Diethoxyacetaldehyd‐SAMP‐Hydrazon Angewandte Chemie. 105: 418-420. DOI: 10.1002/Ange.19931050314  0.473
1992 Enders D, Meyer O, Raabe G. Diastereo- and Enantioselective Synthesis of 4-Nitrocyclohexanones by [4+2] Cycloaddition of a Chiral 2-Aminobutadiene to Nitroalkenes Synthesis. 1992: 1242-1244. DOI: 10.1055/S-1992-26349  0.485
1992 Enders D, Jegelka U. Flexible and Stereocontrolled Synthesis of Azasugars with Novel Substitution Patterns Synlett. 1992: 999-1002. DOI: 10.1055/S-1992-21562  0.419
1992 Enders D, Dyker H, Raabe G, Runsink J. Enantio- and Diastereoselective Synthesis of 3-Substituted Cyclic Hemiketals of ω-Hydroxy-2-oxoesters Synlett. 1992: 901-903. DOI: 10.1055/S-1992-21534  0.533
1992 Enders D, Zamponi A, Raabe G. Enantioselective synthesis of 3-oxoesters and carboxylic acids as polyfunctional small building blocks with a quaternary stereogenic center Synlett. 1992: 897-900. DOI: 10.1055/S-1992-21533  0.424
1992 Enders D, Karl W. β-Lithiated Enamines as Enolate Equivalents in Asymmetric Michael Additions to Enoates. Highly Enantioselective Synthesis of Mono- and Disubstituted 5-Oxo Esters Synlett. 1992: 895-897. DOI: 10.1055/S-1992-21532  0.498
1992 Enders D, Pathak VN, Weuster P. Regioselective Acylations of Ketones to 1,3-Diketones via Metalated Dimethylhydrazones[1] Chemische Berichte. 125: 515-524. DOI: 10.1002/Cber.19921250232  0.428
1992 Enders D, Dyker H, Raabe G. Enantioselective Synthesis of 3-Substituted 2-Ketoesters Angewandte Chemie International Edition in English. 31: 618-620. DOI: 10.1002/anie.199206181  0.462
1992 Enders D, Dyker H, Raabe G. Enantioselektive Synthese 3-substituierter 2-Ketoester Angewandte Chemie. 104: 649-651. DOI: 10.1002/Ange.19921040535  0.421
1991 Enders D, Gatzweiler W, Jegelka U. Diastereo- and enantioselective synthesis of α,α'-disubstituted, C2-symmetric ketones using the SAMP-/RAMP-hydrazone method Synthesis. 1991: 1137-1141. DOI: 10.1055/S-1991-28405  0.413
1991 Duhamel L, Duhamel P, Enders D, Karl W, Leger F, Poirier JM, Raabe G. β-Lithiated Enamines as Enolate Equivalents in Michael Additions to Enoates. A Novel Entry to Mono- and Disubstituted 5-Oxo Esters Synthesis. 1991: 649-654. DOI: 10.1055/S-1991-26536  0.417
1991 Enders D, Plant A. Enantioselective synthesis of (S)‐(+)‐2‐tridecanol acetate, an aggregation pheromone component of Drosophila mulleri European Journal of Organic Chemistry. 1991: 1241-1243. DOI: 10.1002/Jlac.1991199101214  0.449
1991 Enders D, Bartzen D. Enantioselective total synthesis of harmonine, a defence alkaloid of ladybugs (Coleoptera: Coccinellidae) Liebigs Annalen Der Chemie. 1991: 569-574. DOI: 10.1002/jlac.1991199101103  0.414
1991 Enders D, Nakai S. Regio-, Diastereo-, and Enantioselective Synthesis ofvic-Diols via α-Silyl Ketones According to the SAMP/RAMP Hydrazone Method Chemische Berichte. 124: 219-226. DOI: 10.1002/Cber.19911240133  0.48
1991 Enders D, Scherer HJ, Raabe G. Diastereo- And Enantioselective Michael Addition Initiated Cyclizations Totrans-Substituted Cyclopentanecarboxylates Angewandte Chemie. 30: 1664-1666. DOI: 10.1002/Anie.199116641  0.541
1990 Enders D, Dahmen W, Dederichs E, Gatzweiler W, Weuster P. Synthesis of spiroacetal pheromones via metalated hydrazones Synthesis. 1990: 1013-1019. DOI: 10.1055/S-1990-27080  0.46
1990 Enders D, Gatzweiler W, Dederichs E. Diastereo- and enantioselective synthesis of α,α'-Disubstituted spiroacetals using the SAMP-/RAMP-hydrazone method Tetrahedron. 46: 4757-4792. DOI: 10.1016/S0040-4020(01)85594-0  0.399
1990 Keim W, Koehnes A, Roethel T, Enders D. Enantioselective telomerization. I. Telomerization of butadiene with formaldehyde, β-dicarbonyl compounds, nitroalkanes, and enamines Journal of Organometallic Chemistry. 382: 295-301. DOI: 10.1016/0022-328X(90)85233-O  0.464
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