Highly Stereoselective Aldol Condensation Using an Enantioselective Chiral Enolate
- 1 July 1980
- journal article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 19 (7) , 557-558
- https://doi.org/10.1002/anie.198005571
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Acyclic stereoselection. 6. A reagent for achieving high 1,2-diastereoselection in the aldol conversion of chiral aldehydes into 3-hydroxy-2-methylcarboxylic acidsJournal of the American Chemical Society, 1979
- Acyclic stereoselection. 5. Use of double stereodifferentiation to enhance 1,2 diastereoselection in aldol condensations of chiral aldehydesJournal of the American Chemical Society, 1979
- Diastereoselective Synthesis of β‐Methyl Homoallyl AlcoholsAngewandte Chemie International Edition in English, 1979
- Diastereoselektive Synthese von β‐Methyl‐homoallylalkoholenAngewandte Chemie, 1979
- New Approaches in Asymmetric SynthesisTopics in Stereochemistry, 1979
- Acyclic stereoselection. 2. Synthesis of 3-hydroxy-2-methyl- and 3-hydroxy-2,4-dimethylcarboxylic acidsJournal of the American Chemical Society, 1977
- Studies in Stereochemistry. XX. Steric Control of Asymmetric Induction in the Preparation of the 3-Cyclohexyl-2-butanol System1Journal of the American Chemical Society, 1953
- LXXX.—Experiments on the Walden inversion. Part IV. The interconversion of the optically active phenylmethylglycollic acidsJournal of the Chemical Society, Transactions, 1910