Palladium-Catalyzed Amination/Dearomatization Reaction of Indoles and Benzofurans.


Journal

The Journal of organic chemistry
ISSN: 1520-6904
Titre abrégé: J Org Chem
Pays: United States
ID NLM: 2985193R

Informations de publication

Date de publication:
19 06 2020
Historique:
pubmed: 23 5 2020
medline: 23 5 2020
entrez: 23 5 2020
Statut: ppublish

Résumé

This report describes a palladium-catalyzed dearomatization and amination tandem reaction of 2,3-disubstituted indoles and benzofurans via the Catellani strategy. This reaction provides a new method for the construction of amino-substituted indoline-fused cyclic and benzofuran spiro compounds in good yields. The reaction has broad functional group compatibility and substrate scope.

Identifiants

pubmed: 32441518
doi: 10.1021/acs.joc.0c00475
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

7817-7839

Auteurs

Zhe Zhang (Z)

State key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, China.

Bo-Sheng Zhang (BS)

State key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, China.

Kai-Li Li (KL)

Lanzhou University Second Clinical Medical College, Lanzhou 730000, China.

Yang An (Y)

State key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, China.

Ce Liu (C)

State key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, China.

Xue-Ya Gou (XY)

State key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, China.

Yong-Min Liang (YM)

State key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, China.

Classifications MeSH