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New stable reagents for the nucleophilic trifluoromethylation. Part 4: Trifluoromethylation of disulfides and diselenides with hemiaminals of trifluoroacetaldehyde

✍ Scribed by G Blond; T Billard; B.R Langlois

Book ID
104230299
Publisher
Elsevier Science
Year
2001
Tongue
French
Weight
60 KB
Volume
42
Category
Article
ISSN
0040-4039

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πŸ“œ SIMILAR VOLUMES

New stable reagents for the nucleophilic
New stable reagents for the nucleophilic trifluoromethylation. Part 2: Trifluoromethylation with silylated hemiaminals of trifluoroacetaldehyde
✍ T Billard; B.R Langlois*; G Blond πŸ“‚ Article πŸ“… 2000 πŸ› Elsevier Science 🌐 French βš– 102 KB

New reagents for the nucleophilic trifluoromethylation have been easily synthesized from fluoral hemiketal. They provide silylated trifluoromethylcarbinol from non-enolizable carbonyl compounds.

ChemInform Abstract: New Stable Reagents
ChemInform Abstract: New Stable Reagents for the Nucleophilic Trifluoromethylation. Part 1. Trifluoromethylation of Carbonyl Compounds with N-Formylmorpholine Derivatives.
✍ T. Billard; S. Bruns; B. R. Langlois πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons βš– 33 KB πŸ‘ 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v