Reformatsky Reaction of Methyl 2-Bromo-3,3,3-trifluoropropanoate. A Synthetic Method for α-Trifluoromethyl-β-hydroxy Esters
- 5 October 1987
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 16 (10) , 1971-1974
- https://doi.org/10.1246/cl.1987.1971
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- -Acylation and -allylation of β,β,β-trifluoropropionic esters via the ketene silyl acetalsTetrahedron Letters, 1984
- (Trifluoromethyl)ketene silyl acetal as an equivalent to the trifluoropropionic ester enolate: preparation and aldol-type reactions with acetalsTetrahedron Letters, 1984
- Organic sonochemistry. Sonic acceleration of the Reformatsky reactionThe Journal of Organic Chemistry, 1982
- Simple o-quinodimethane route to (.+-.)-4-demethoxydaunomycinoneJournal of the American Chemical Society, 1981
- Synthetic methods. IV. Halogenation of carbonyl compounds via silyl enol ethersThe Journal of Organic Chemistry, 1974
- Reformatsky reaction at room temperature and in the presence of trimethylborate. Improved procedures for the preparation of .beta.-hydroxy estersThe Journal of Organic Chemistry, 1970