Nickel-Catalyzed Deoxygenative Amidation of Alcohols with Carbamoyl Chlorides.


Journal

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

Informations de publication

Date de publication:
11 Mar 2024
Historique:
medline: 11 3 2024
pubmed: 11 3 2024
entrez: 11 3 2024
Statut: aheadofprint

Résumé

We report a deoxygenative amidation reaction of alcohols with carbamoyl chlorides to afford amides through nickel-photoredox dual catalysis. Good to excellent yields can be obtained even for diverse complex sugar and steroid derivatives. The reaction is scalable, and the synthetic utility of the reaction was demonstrated by the homologation of alcohols to deliver several important γ-amino alcohols and a synthetically challenging bioactive compound intermediate.

Identifiants

pubmed: 38465891
doi: 10.1021/acs.orglett.4c00519
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Lele Wang (L)

College of Chemistry and Molecular Sciences, Wuhan University, 299 Bayi Road, Wuhan 430072, P. R. China.

Zhongxian Li (Z)

College of Chemistry and Molecular Sciences, Wuhan University, 299 Bayi Road, Wuhan 430072, P. R. China.

Yang Zhou (Y)

College of Chemistry and Molecular Sciences, Wuhan University, 299 Bayi Road, Wuhan 430072, P. R. China.

Jun Zhu (J)

College of Chemistry and Molecular Sciences, Wuhan University, 299 Bayi Road, Wuhan 430072, P. R. China.

Classifications MeSH