Asymmetric Direct Aldol Reaction Assisted by Water and a Proline‐Derived Tetrazole Catalyst
- 30 March 2004
- journal article
- zuschrift
- Published by Wiley in Angewandte Chemie
- Vol. 116 (15), 2017-2020
- https://doi.org/10.1002/ange.200352724
Abstract
No abstract availableKeywords
This publication has 53 references indexed in Scilit:
- Biogenetically Inspired Approach to the Strychnos Alkaloids. Concise Syntheses of (±)-Akuammicine and (±)-StrychnineJournal of the American Chemical Society, 2001
- Catalytic asymmetric homo-aldol reaction of pyruvate—a chiral Lewis acid catalyst that mimics aldolase enzymesChemical Communications, 2000
- Simple Metal Alkoxides as Effective Catalysts for the Hetero-Aldol−Tishchenko ReactionOrganic Letters, 1999
- Direct Aldol Reactions of Glycoxylic Acid Monohydrate with KetonesSynlett, 1999
- Highly Regioselective Lewis Acid-Mediated Aldol Additions at the More Encumbered α-Side of Unsymmetrical KetonesJournal of the American Chemical Society, 1998
- Synthesis and biological activity of carboxylic acid replacement analogs of the potent angiotensin converting enzyme inhibitor 5(S)-benzamido-4-oxo-6-phenylhexanoyl-L-prolineJournal of Medicinal Chemistry, 1985
- New Type of Aldol Condensations Catalyzed by Metal(II) Complexes of α-Amino Acid Esters and that with Cyclodextrin SystemBulletin of the Chemical Society of Japan, 1985
- The absolute configuration of 4-(trichloromethyl)oxetan-2-one; a case of double anchimeric assistance with inversionJournal of the Chemical Society, Chemical Communications, 1984
- Lewis acid catalysis of the ene addition of chloral and bromal to olefins; product studiesJournal of the Chemical Society, Perkin Transactions 1, 1984
- Stereospecific total synthesis of the potent synthetic pyrethroid NRDC 182The Journal of Organic Chemistry, 1980