Synthesis of Chiral α-Hydroxyphenyl Crotonates
- 1 March 1991
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 21 (6) , 727-732
- https://doi.org/10.1080/00397919108019751
Abstract
By making use of (S) (+)-prolinol as chiral auxiliary methyl crotonate is converted to a chiral α-hydroxyaryl derivative in 50% e.e.Keywords
This publication has 9 references indexed in Scilit:
- Chiral acrylates as substrates in baylis-hillman reactionTetrahedron Letters, 1990
- Terminal Hydroxyalkyl Acrylates as Substrates for Baylis-Hillman ReactionSynthetic Communications, 1990
- Stereoselective epoxidation of hydroxyenones. The synthesis of the sidechain of clerocidinTetrahedron Letters, 1990
- Rate Enhancement Effects in the Dabco Catalysed Synthesis of Hydroxyalkenoate EstersSynthetic Communications, 1988
- Synthetic potential of the tertiary-amine-catalysed reaction of activated vinyl carbanions with aldehydesTetrahedron, 1988
- Double Asymmetric Synthesis and a New Strategy for Stereochemical Control in Organic SynthesisAngewandte Chemie International Edition in English, 1985
- 13C nuclear magnetic resonance spectra of the Senecio alkaloids, retrorsine, swazine, isoline, and hygrophyllineJournal of the Chemical Society, Perkin Transactions 1, 1981
- Synthesis of new macrocycles. Part 6. Pyridine-retronecate, a new synthetic alkaloidJournal of the Chemical Society, Perkin Transactions 1, 1981
- Correlation of configuration of chiral secondary carbinols by use of a chiral lanthanide nuclear magnetic resonance shift reagentThe Journal of Organic Chemistry, 1974