Dehydroxylative Fluorination of Tertiary Alcohols.

Journal

Organic letters
ISSN: 1523-7052
Titre abrégé: Org Lett
Pays: United States
ID NLM: 100890393

Informations de publication

Date de publication:
21 Aug 2020
Historique:
pubmed: 19 8 2020
medline: 19 8 2020
entrez: 19 8 2020
Statut: ppublish

Résumé

A large number of fluorination methods have been developed, but the construction of a tertiary C-F bond remains challenging. Herein, we describe an efficient dehydroxylative fluorination of tertiary alcohols with Selectfluor via the activation of a hydroxyl group by a Ph

Identifiants

DOI: 10.1021/acs.orglett.0c02438 PMID: 32806144
pubmed: 32806144
doi: 10.1021/acs.orglett.0c02438
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

6642-6646

Auteurs

Wei Zhang (W)

Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.

Yu-Cheng Gu (YC)

Syngenta, Jealott's Hill International Research Centre, Bracknell, Berkshire RG426EY, U.K.

Jin-Hong Lin (JH)

Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.
ORCID: 0000-0002-7000-9540

Ji-Chang Xiao (JC)

Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.
ORCID: 0000-0001-8881-1796

Classifications MeSH