Difluorocarbene-derived trifluoromethylselenolation of benzyl halides.


Journal

Chemical communications (Cambridge, England)
ISSN: 1364-548X
Titre abrégé: Chem Commun (Camb)
Pays: England
ID NLM: 9610838

Informations de publication

Date de publication:
29 Jan 2019
Historique:
pubmed: 15 1 2019
medline: 15 1 2019
entrez: 15 1 2019
Statut: ppublish

Résumé

Cu-Promoted difluorocarbene-derived trifluoromethylselenolation of benzyl halides with the Ph3P+CF2CO2-/Se/F- system is described. Three new carbon-heteroatom bonds, a Se-CF2 bond, SeCF2-F bond, and C-SeCF3 bond, were sequentially formed in the reaction. This work represents the first trifluoromethylselenolation protocol involving an external fluoride for the generation of the key intermediate, CF3Se- anion.

Identifiants

pubmed: 30640337
doi: 10.1039/c8cc09719d
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1410-1413

Auteurs

Xin-Lei Chen (XL)

College of Chemistry and Materials Science, Shanghai Normal University, 100 Guilin Road, Shanghai, 200234, China. qinghaideng@shnu.edu.cn.

Classifications MeSH