The Origin of Stereoselectivity in Primary Amino Acid Catalyzed Intermolecular Aldol Reactions
- 31 October 2005
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 44 (43), 7028-7032
- https://doi.org/10.1002/anie.200502388
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- Amino Acid Catalyzed Neogenesis of Carbohydrates: A Plausible Ancient TransformationChemistry – A European Journal, 2005
- Theoretical Studies of Stereoselectivities of Intramolecular Aldol Cyclizations Catalyzed by Amino AcidsJournal of the American Chemical Society, 2005
- Acyclic amino acid-catalyzed direct asymmetric aldol reactions: alanine, the simplest stereoselective organocatalystChemical Communications, 2005
- Plausible origins of homochirality in the amino acid catalyzed neogenesis of carbohydratesChemical Communications, 2005
- Computational Evidence for the Enamine Mechanism of Intramolecular Aldol Reactions Catalyzed by ProlineAngewandte Chemie, 2004
- In the Golden Age of OrganocatalysisAngewandte Chemie International Edition, 2004
- Prebiotic Amino Acids as Asymmetric CatalystsScience, 2004
- Enantioselective total synthesis of a protosterol, 3.beta.,20-dihydroxyprotost-24-eneJournal of the American Chemical Society, 1990
- Pyridine route to optically active estrone and 19-norsteroidsJournal of the American Chemical Society, 1975
- New Type of Asymmetric Cyclization to Optically Active Steroid CD Partial StructuresAngewandte Chemie International Edition in English, 1971