Asymmetric Catalytic Epoxydation by Means of Cyclodextrins
- 1 October 1983
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 13 (12) , 1049-1052
- https://doi.org/10.1080/00397918308082725
Abstract
Asymmetric synthesis occurs in the epoxidation of trans-chalcone with sodium hypochlorite and cyclodextrins, with enantiomeric excess up to 11%.Keywords
This publication has 3 references indexed in Scilit:
- Biomimetic control of chemical selectivityAccounts of Chemical Research, 1980
- Absolute configuration of chalcone epoxide. Chemical correlationThe Journal of Organic Chemistry, 1979
- Conformation of O-methylated amylose and cyclodextrinsTetrahedron, 1968