Rh(iii)-Catalyzed regioselective C4 alkylation of indoles with allylic alcohols: direct access to β-indolyl ketones.


Journal

Organic & biomolecular chemistry
ISSN: 1477-0539
Titre abrégé: Org Biomol Chem
Pays: England
ID NLM: 101154995

Informations de publication

Date de publication:
29 04 2020
Historique:
pubmed: 4 4 2020
medline: 4 4 2020
entrez: 4 4 2020
Statut: ppublish

Résumé

A Rh(iii)-catalyzed and weak coordination carbonyl guided direct C4 alkylation of indoles with allylic alcohols was developed with excellent regioselectivity. This reaction was conducted under mild conditions, leading to a variety of β-indolyl ketones with good functional group tolerance in moderate to good yields.

Identifiants

pubmed: 32242601
doi: 10.1039/d0ob00396d
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

3038-3042

Auteurs

Changduo Pan (C)

School of Chemical and Environmental Engineering, Jiangsu University of Technology, Changzhou 213001, P. R. China. panchangduo@jsut.edu.cn.

Gao Huang (G)

School of Petrochemical Engineering, Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, Changzhou University, Changzhou 213164, P. R. China. yujintao@cczu.edu.cn.

Yujia Shan (Y)

School of Petrochemical Engineering, Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, Changzhou University, Changzhou 213164, P. R. China. yujintao@cczu.edu.cn.

Yiting Li (Y)

School of Petrochemical Engineering, Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, Changzhou University, Changzhou 213164, P. R. China. yujintao@cczu.edu.cn.

Jin-Tao Yu (JT)

School of Petrochemical Engineering, Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, Changzhou University, Changzhou 213164, P. R. China. yujintao@cczu.edu.cn.

Classifications MeSH