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A rapid and selective synthesis of α,α-fluorohalo esters via fluorohalogenative or difluorinative hydration of ynol ethers.
- Source :
-
Chemical Communications . 12/4/2015, Vol. 51 Issue 93, p16641-16644. 4p. - Publication Year :
- 2015
-
Abstract
- A Selectfluor-mediated fluorohalogenative or difluorinative hydration of ynol ethers is described, giving various α,α-fluorohalo esters including α,α-bromofluoro, α,α-chlorofluoro, α,α-fluoroiodo, and α,α-difluoro derivatives in a highly selective manner under very mild reaction conditions. The resultant products can be applied to the facile synthesis of α-monofluoro-α-amino acids. This reaction represents a new advance in the trifunctionalization of alkynes. [ABSTRACT FROM AUTHOR]
- Subjects :
- *HYDRATION
*HALOGENATION
*CARBONYL compounds
*CHEMICAL reactions
*YNOLS
*ETHERS
Subjects
Details
- Language :
- English
- ISSN :
- 13597345
- Volume :
- 51
- Issue :
- 93
- Database :
- Academic Search Index
- Journal :
- Chemical Communications
- Publication Type :
- Academic Journal
- Accession number :
- 110841343
- Full Text :
- https://doi.org/10.1039/c5cc07471a