The Unambiguous Specification of the Steric Course of Asymmetric Syntheses
- 1 September 1982
- journal article
- review article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 21 (9) , 654-660
- https://doi.org/10.1002/anie.198206541
Abstract
No abstract availableKeywords
This publication has 61 references indexed in Scilit:
- Diastereoselective Synthesis of Nitroaldol DerivativesHelvetica Chimica Acta, 1982
- Enantioselective Generation and Diastereoselective Reactions of Chiral Enolates Derived from α‐Heterosubstituted Carboxylic Acids. Preliminary CommunicationHelvetica Chimica Acta, 1981
- Vanadium-catalyzed epoxidations. 2. Highly stereoselective epoxidations of acyclic homoallylic alcohols predicted by a detailed transition-state modelJournal of the American Chemical Society, 1981
- Diastereoselektive Aldol–ReaktionenNachrichten aus Chemie, Technik und Laboratorium, 1981
- Highly Stereoselective Aldol Condensation Using an Enantioselective Chiral EnolateAngewandte Chemie International Edition in English, 1980
- Über die Stereospezifität der α‐Alkylierung von β‐Hydroxycarbonsäureestern. Vorläufige MitteilungHelvetica Chimica Acta, 1979
- Highly stereoselective addition of organolithium reagents to chiral oxazolines. Asymmetric synthesis of 3-substituted alkanoic acids and 3-substituted lactonesThe Journal of Organic Chemistry, 1979
- Studies in Stereochemistry. XXXII. Models for 1,2-Asymmetric InductionJournal of the American Chemical Society, 1963
- Studies in Stereochemistry. X. The Rule of “Steric Control of Asymmetric Induction” in the Syntheses of Acyclic SystemsJournal of the American Chemical Society, 1952
- PARTIALLY ASYMMETRIC MEERWEIN-PONNDORF-VERLEY REDUCTIONSJournal of the American Chemical Society, 1950