TY - JOUR AU - List, B. AU - Yang, J. W. TI - The organic approach to asymmetric catalysis JA - Science PY - 2006/// VL - 313 SP - 1584 EP - 1586 PB - Nature Publishing Group M3 - 10.1126/science.1131945 N1 - 10.1126/science.1131945 UR - http://dx.doi.org/10.1126/science.1131945 ER - TY - JOUR AU - Mukherjee, S. AU - Yang, J. W. AU - Hoffmann, S. AU - List, B. TI - Asymmetric enamine catalysis JA - Chem. Rev. PY - 2007/// VL - 107 SP - 5471 EP - 5569 PB - Nature Publishing Group M3 - 10.1021/cr0684016 N1 - 10.1021/cr0684016 UR - http://dx.doi.org/10.1021/cr0684016 ER - TY - JOUR AU - Cordova, A. AU - Notz, W. AU - Barbas, C. F. TI - Proline-catalyzed one-step asymmetric synthesis of 5-hydroxy (2E)-hexenal from acetaldehyde JA - J. Org. Chem. PY - 2002/// VL - 67 SP - 301 EP - 303 PB - Nature Publishing Group M3 - 10.1021/jo015881m N1 - 10.1021/jo015881m UR - http://dx.doi.org/10.1021/jo015881m ER - TY - JOUR AU - Bogevig, A. AU - Kumaragurubaran, N. AU - Jorgensen, K. A. TI - Direct catalytic asymmetric aldol reactions of aldehydes JA - Chem. Commun. PY - 2002/// SP - 620 EP - 621 PB - Nature Publishing Group ER - TY - JOUR AU - Machajewski, T. D. AU - Wong, C.-H. TI - The catalytic asymmetric aldol reaction JA - Angew. Chem. Int. Edn Engl. PY - 2000/// VL - 39 SP - 1352 EP - 1375 PB - Nature Publishing Group M3 - 10.1002/(SICI)1521-3773(20000417)39:8<1352::AID-ANIE1352>3.0.CO;2-J N1 - 10.1002/(SICI)1521-3773(20000417)39:8<1352::AID-ANIE1352>3.0.CO;2-J UR - http://dx.doi.org/10.1002/(SICI)1521-3773(20000417)39:8<1352::AID-ANIE1352>3.0.CO;2-J ER - TY - JOUR AU - Goetz, G. AU - Iwan, P. AU - Hauer, B. AU - Breuer, M. AU - Pohl, M. TI - Continuous production of (R)-phenylacetylcarbinol in an enzyme-membrane reactor using a potent mutant of pyruvate decarboxylase from Zymomonas mobilis JA - Biotechnol. Bioeng. PY - 2001/// VL - 74 SP - 317 EP - 325 PB - Nature Publishing Group M3 - 10.1002/bit.1122 N1 - 10.1002/bit.1122 UR - http://dx.doi.org/10.1002/bit.1122 ER - TY - JOUR AU - Enders, D. AU - Rendenbach, B. E. M. TI - Asymmetric Michael additions via SAMP-/RAMP-hydrazones enantioselective synthesis of [bgr]-substituted [dgr]-oxopentanoates and [dgr]-lactones JA - Chem. Ber. PY - 1987/// VL - 120 SP - 1223 EP - 1227 PB - Nature Publishing Group M3 - 10.1002/cber.19871200718 N1 - 10.1002/cber.19871200718 UR - http://dx.doi.org/10.1002/cber.19871200718 ER - TY - JOUR AU - Denmark, S. E. AU - Bui, T. TI - Lewis base catalyzed enantioselective aldol addition of acetaldehyde-derived silyl enol ether to aldehydes JA - J. Org. Chem. PY - 2005/// VL - 70 SP - 10190 EP - 10193 PB - Nature Publishing Group M3 - 10.1021/jo0517500 N1 - 10.1021/jo0517500 UR - http://dx.doi.org/10.1021/jo0517500 ER - TY - JOUR AU - Boxer, M. B. AU - Yamamoto, H. TI - Tris(trimethylsilyl)silyl-governed aldehyde cross-aldol cascade reaction JA - J. Am. Chem. Soc. PY - 2006/// VL - 128 SP - 48 EP - 49 PB - Nature Publishing Group M3 - 10.1021/ja054725k N1 - 10.1021/ja054725k UR - http://dx.doi.org/10.1021/ja054725k ER - TY - JOUR AU - List, B. TI - The direct catalytic asymmetric three-component Mannich reaction JA - J. Am. Chem. Soc. PY - 2000/// VL - 122 SP - 9336 EP - 9337 PB - Nature Publishing Group M3 - 10.1021/ja001923x N1 - 10.1021/ja001923x UR - http://dx.doi.org/10.1021/ja001923x ER - TY - JOUR AU - Enders, D. AU - Vrettou, M. TI - Asymmetric synthesis of (+)-polyoxamic acid via an efficient organocatalytic Mannich reaction as the key step JA - Synthesis PY - 2006/// SP - 2155 EP - 2158 PB - Nature Publishing Group ER - TY - JOUR AU - Yang, J. W. AU - Stadler, M. AU - List, B. TI - Proline-catalyzed Mannich reaction of aldehydes with N-Boc-imines JA - Angew. Chem. Int. Edn Engl. PY - 2007/// VL - 46 SP - 609 EP - 611 PB - Nature Publishing Group M3 - 10.1002/anie.200603188 N1 - 10.1002/anie.200603188 UR - http://dx.doi.org/10.1002/anie.200603188 ER - TY - JOUR AU - Porter, E. A. AU - Wang, X. AU - Lee, H.-S. AU - Weisblum, B. AU - Gellman, S. H. TI - Non-haemolytic [bgr]-amino-acid oligomers JA - Nature PY - 2000/// VL - 404 SP - 565 PB - Nature Publishing Group M3 - 10.1038/35007145 N1 - 10.1038/35007145 UR - http://dx.doi.org/10.1038/35007145 ER - TY - JOUR AU - Seebach, D. TI - Synthesis of [bgr]-hexa- and [bgr]-heptapeptides containing novel [bgr]2,3-amino acids with two serine or two cysteine side chains -CD- and NMR-spectroscopic evidence for 314-helical secondary structures in water JA - Helv. Chim. Acta PY - 2000/// VL - 83 SP - 2115 EP - 2140 PB - Nature Publishing Group M3 - 10.1002/1522-2675(20000906)83:9<2115::AID-HLCA2115>3.0.CO;2-E N1 - 10.1002/1522-2675(20000906)83:9<2115::AID-HLCA2115>3.0.CO;2-E UR - http://dx.doi.org/10.1002/1522-2675(20000906)83:9<2115::AID-HLCA2115>3.0.CO;2-E ER - TY - JOUR AU - Ramachandran, P. V. AU - Burghardt, T. E. TI - Highly diastereoselective and enantioselective preparation of homoallylic amines: application for the synthesis of [bgr]-amino acids and [ggr]-lactams JA - Chem. Eur. J. PY - 2005/// VL - 11 SP - 4387 EP - 4395 PB - Nature Publishing Group M3 - 10.1002/chem.200401295 N1 - 10.1002/chem.200401295 UR - http://dx.doi.org/10.1002/chem.200401295 ER - TY - JOUR AU - Chi, Y. TI - Practical synthesis of enantiomerically pure [bgr]2-amino acids via proline-catalyzed diastereoselective aminomethylation of aldehydes JA - J. Am. Chem. Soc. PY - 2007/// VL - 129 SP - 6050 EP - 6055 PB - Nature Publishing Group M3 - 10.1021/ja070063i N1 - 10.1021/ja070063i UR - http://dx.doi.org/10.1021/ja070063i ER - TY - JOUR AU - Sorbera, L. A. AU - Castaner, J. AU - Castaner, R. M. TI - Dapoxetine hydrochloride JA - Drugs Fut. PY - 2004/// VL - 29 SP - 1201 EP - 1205 PB - Nature Publishing Group M3 - 10.1358/dof.2004.029.12.865936 N1 - 10.1358/dof.2004.029.12.865936 UR - http://dx.doi.org/10.1358/dof.2004.029.12.865936 ER - TY - JOUR AU - Siddiqui, S. A. AU - Srinivasan, K. V. TI - Enantioselective synthesis of (S)-dapoxetine JA - Tetrahedr. Asymm. PY - 2007/// VL - 18 SP - 2099 EP - 2103 PB - Nature Publishing Group M3 - 10.1016/j.tetasy.2007.07.028 N1 - 10.1016/j.tetasy.2007.07.028 UR - http://dx.doi.org/10.1016/j.tetasy.2007.07.028 ER - TY - JOUR AU - Davies, S. G. TI - Oxazinanones as chiral auxiliaries: synthesis and evaluation in enolate alkylations and aldol reactions JA - Org. Biomol. Chem. PY - 2006/// VL - 4 SP - 2753 EP - 2768 PB - Nature Publishing Group M3 - 10.1039/b604073j N1 - 10.1039/b604073j UR - http://dx.doi.org/10.1039/b604073j ER - TY - JOUR AU - Dorr, P. TI - Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity JA - Antimicrob. Agents Chemother. PY - 2005/// VL - 49 SP - 4721 EP - 4732 PB - Nature Publishing Group M3 - 10.1128/AAC.49.11.4721-4732.2005 N1 - 10.1128/AAC.49.11.4721-4732.2005 UR - http://dx.doi.org/10.1128/AAC.49.11.4721-4732.2005 ER - TY - JOUR AU - Price, D. A. TI - Initial synthesis of UK-427,857 (Maraviroc) JA - Tetrahedr. Lett. PY - 2005/// VL - 46 SP - 5005 EP - 5007 PB - Nature Publishing Group M3 - 10.1016/j.tetlet.2005.05.082 N1 - 10.1016/j.tetlet.2005.05.082 UR - http://dx.doi.org/10.1016/j.tetlet.2005.05.082 ER - TY - JOUR AU - Davis, F. A. AU - Szewczyk, J. M. TI - Synthesis and applications of nonracemic [bgr]-amino aldehydes to the asymmetric synthesis of piperdines: (+)-dihydropinidine JA - Tetrahedr. Lett. PY - 1998/// VL - 39 SP - 5951 EP - 5954 PB - Nature Publishing Group M3 - 10.1016/S0040-4039(98)01223-4 N1 - 10.1016/S0040-4039(98)01223-4 UR - http://dx.doi.org/10.1016/S0040-4039(98)01223-4 ER - TY - GEN AU - Fodor, G. B. AU - Colasanti, B. TI - Alkaloids: Chemical and Biological Perspectives PY - 1985/// SP - 1 EP - 90 PB - Nature Publishing Group ER - TY - JOUR AU - Song, J. AU - Wang, Y. AU - Deng, L. TI - The Mannich reaction of malonates with simple imines catalyzed by bifunctional cinchona alkaloids: enantioselective synthesis of [bgr]-amino acids JA - J. Am. Chem. Soc. PY - 2006/// VL - 128 SP - 6048 EP - 6049 PB - Nature Publishing Group M3 - 10.1021/ja060716f N1 - 10.1021/ja060716f UR - http://dx.doi.org/10.1021/ja060716f ER -