Stereospecific Preparation of Transglycidic Esters
- 1 January 1989
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 19 (1-2) , 221-232
- https://doi.org/10.1080/00397918908050973
Abstract
Trans-disubstituted glycidic esters have been prepared stereospecifically by reaction of the dicyclopentylboryl enolate of α-bromo-t-butylthioacetate with aromatic aldehydes.Keywords
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