New stable reagents for the nucleophilic trifluoromethylation. Part 2: Trifluoromethylation with silylated hemiaminals of trifluoroacetaldehyde

Authors
Billard, T Langlois, BR Blond, G
Citation
T. Billard et al., New stable reagents for the nucleophilic trifluoromethylation. Part 2: Trifluoromethylation with silylated hemiaminals of trifluoroacetaldehyde, TETRAHEDR L, 41(45), 2000, pp. 8777-8780
Citations number
6
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
41
Issue
45
Year of publication
2000
Pages
8777 - 8780
Database
ISI
SICI code
0040-4039(20001104)41:45<8777:NSRFTN>2.0.ZU;2-D
Abstract
New reagents for the nucleophilic trifluoromethylation have been easily syn thesized from fluoral hemiketal. They provide silylated trifluoromethylcarb inol from non-enolizable carbonyl compounds. (C) 2000 Elsevier Science Ltd. All rights reserved.