REACTION OF VINYLOXYTIN. A NEW METHOD FOR THE PREPARATION OF β-HYDROXYALKANOATE
- 5 July 1974
- journal article
- research article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 3 (7) , 689-690
- https://doi.org/10.1246/cl.1974.689
Abstract
It was suggested that vinyloxytin was produced by passing gaseous ketene into a methylene chloride solution of tin alkoxide at low temperature. The vinyloxytin thus formed further reacted with various carbonyl compounds at low temperature in the presence of strong Lewis acid such as TiCl4, or AlCl3 to give the corresponding β-hydroxyalkanoates.Keywords
This publication has 1 reference indexed in Scilit:
- Reactions of Vinyloxyboranes. A Convenient Method for the Preparation of β-Hydroxy Thiolesters, Esters and KetonesBulletin of the Chemical Society of Japan, 1973