Trifluoromethyl group induced highly stereoselective synthesis of α-hydroxy carbonyl compounds
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
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2. -Acylation and -allylation of β,β,β-trifluoropropionic esters via the ketene silyl acetals
3. Determination of the structure of the adduct from guanosine and glycidaldehyde
4. Preparation of alpha-fluoroenolates and their use in the directed aldol reaction
5. Facile diastereoselective ester enolate Claisen rearrangements of allyl fluoroacetates
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4. The Use of Fluoride as a Leaving Group: SN2′ Displacement of a CF Bond on 3,3-Difluoropropenes with Organolithium Reagents To Give Direct Access to Monofluoroalkenes;Angewandte Chemie International Edition;2011-09-28
5. The Use of Fluoride as a Leaving Group: SN2′ Displacement of a CF Bond on 3,3-Difluoropropenes with Organolithium Reagents To Give Direct Access to Monofluoroalkenes;Angewandte Chemie;2011-09-28
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