Thiol Esters in Organic Synthesis. XV. Reduction with Tetrabutylammonium Borohydride
- 1 February 1989
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 19 (3-4) , 387-392
- https://doi.org/10.1080/00397918908050678
Abstract
Treatment of thiol esters with tetrabutylammonium borohydride in refluxing chloroform gave rise to the corresponding alcohols.Keywords
This publication has 7 references indexed in Scilit:
- Thiol esters in organic synthesis. XIV. The total synthesis of racemic α-costalCanadian Journal of Chemistry, 1986
- Cyanothiolacetate as a masked β-hydroxyproprionitrile carbanion in Michael reactionsCanadian Journal of Chemistry, 1986
- Thiol esters in organic synthesis.Tetrahedron Letters, 1982
- Selective Reduction of Thiol Esters with Sodium BorohydrideSynthetic Communications, 1981
- Direct transformation of carboxylic acids to thiol esters induced by phenyl dichlorophosphateCanadian Journal of Chemistry, 1980
- A facile procedure for the introduction of a hydroxyethyl group. S,S′-Diethyl dithiomalonate as masked ethanol carbanionCanadian Journal of Chemistry, 1979
- Efficiently monitored reduction of carboxylic acids into alcohols or aldehydes via 2-thiazoline-2-thiol esters by sodium borohydride or di-isobutylaluminium hydrideJournal of the Chemical Society, Chemical Communications, 1978