Asymmetric synthesis using α,β-unsaturated sulfoxides. Creation of both (R)- and (S)-asymmetric centers from a single chiral origin.
- 31 March 1976
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 17 (11) , 855-858
- https://doi.org/10.1016/s0040-4039(00)92902-2
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Carbanions α to sulfoxide. Ion-pairing and stereoselectivity.Tetrahedron Letters, 1974
- Oxazolines. XIV. Asymmetric synthesis of R and S dialkylacetic acids from a single chiral oxazolineJournal of the American Chemical Society, 1974
- Asymmetric synthesis using α,β-unsaturated sulfoxides. : A highly selective Michael reactionTetrahedron Letters, 1973
- Conformational preference of an .alpha.-sulfinyl carbanionJournal of the American Chemical Society, 1972
- Solvent effect on the conformational preference of the carbanions derived from benzyl methyl sulfoxideCanadian Journal of Chemistry, 1970