Stereoselective syntheses of γ-hydroxy-α,β-unsaturated esters: An asymmetric version of the “spac” reaction
- 31 December 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (33) , 4325-4328
- https://doi.org/10.1016/s0040-4039(00)99351-1
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Camphor derivatives as chiral auxiliaries in asymmetric synthesisTetrahedron, 1987
- Highly enantioselective rearrangement of (S)-E-α-p-tolysulphinyl-α,β-enoates to (R)-E-γ-hydroxy-α,β-enoatesJournal of the Chemical Society, Chemical Communications, 1986
- Double Asymmetric Synthesis and a New Strategy for Stereochemical Control in Organic SynthesisAngewandte Chemie International Edition in English, 1985
- Facile Synthesis of 4-Hydroxy-(E)-2-alkenoic Esters from AldehydesSynthesis, 1983
- Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) estersJournal of the American Chemical Society, 1973