Asymmetric Aza Friedel-Crafts Reaction of 3,4-Dihydroisoquinolines with 1-Naphthols Catalyzed by Chiral Phosphoric Acids.


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:
10 Oct 2024
Historique:
medline: 11 10 2024
pubmed: 11 10 2024
entrez: 11 10 2024
Statut: aheadofprint

Résumé

An efficient chiral phosphoric acid-catalyzed asymmetric aza Friedel-Crafts reaction of 3,4-dihydroisoquinolines and 1-naphthols is described. The reaction provides a general method for the synthesis of diverse chiral tetrahydroisoquinoline with 1-naphthol substituents at the C1-position in excellent yields and enantioselectivities. Based on the conducted mechanistic experiments, a plausible catalytic mechanism was proposed. Moreover, the practicability of the reaction is successfully demonstrated by its application on a gram scale.

Identifiants

pubmed: 39390820
doi: 10.1021/acs.joc.4c01617
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Ye Zhang (Y)

Sichuan University of Science & Engineering, Zigong 643000, China.

Qiaoyu Gan (Q)

State Key Laboratory of NBC Protection for Civilian, Beijing 102205, China.

Xujin Zhang (X)

Sichuan University of Science & Engineering, Zigong 643000, China.

Xiandong Dai (X)

State Key Laboratory of NBC Protection for Civilian, Beijing 102205, China.

Fanhua Meng (F)

State Key Laboratory of NBC Protection for Civilian, Beijing 102205, China.

Zhenhua Gao (Z)

State Key Laboratory of NBC Protection for Civilian, Beijing 102205, China.

Yujun Si (Y)

Sichuan University of Science & Engineering, Zigong 643000, China.

Yongbiao Guo (Y)

State Key Laboratory of NBC Protection for Civilian, Beijing 102205, China.

Classifications MeSH