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 |
|
Show low-probability matches. |