ALDOL REACTION OF ENOL ACETATES AND LACTOLS WITH N-CHLOROSUCCINIMIDE AND TIN(II) CHLORIDE - DIASTEREOSELECTIVE SYNTHESIS OF DISUBSTITUTED CYCLIC ETHERS

Authors
MASUYAMA Y KOBAYASHI Y KURUSU Y
Citation
Y. Masuyama et al., ALDOL REACTION OF ENOL ACETATES AND LACTOLS WITH N-CHLOROSUCCINIMIDE AND TIN(II) CHLORIDE - DIASTEREOSELECTIVE SYNTHESIS OF DISUBSTITUTED CYCLIC ETHERS, Journal of the Chemical Society, Chemical Communications, (9), 1994, pp. 1123-1123
Citations number
5
Categorie Soggetti
Chemistry
Journal title
Journal of the Chemical Society, Chemical Communications → ACNP
ISSN journal
00224936
Issue
9
Year of publication
1994
Pages
1123 - 1123
Database
ISI
SICI code
0022-4936(1994):9<1123:AROEAA>2.0.ZU;2-J
Abstract
Lactols reacted with enol acetates by a Lewis acid reagent, derived fr om N-chlorosuccinimide and tin(II) chloride, to produce 2-acetonyl cyc lic ethers diastereoselectively.