Radical addition/spirocyclization cascade of tryptamine-derived isocyanides with aryl boronic acids: efficient access to spiroindoline derivatives-Reference-Cited by-同舟云学术

Radical addition/spirocyclization cascade of tryptamine-derived isocyanides with aryl boronic acids: efficient access to spiroindoline derivatives

Published:2023 Issue:7 Volume:10 Page:1660-1668
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Jiang Shuai¹,Huang Yu-Xin¹,Wang Xiao-Feng¹,Xu Xiao-Ping¹²^ORCID,Ji Shun-Jun¹³^ORCID

Affiliation:

1. Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science & Collaborative Innovation Center of Suzhou Nano Science and Technology, Soochow University, Suzhou 215123, People's Republic of China

2. Innovation Center for Chemical Science, Soochow University, Suzhou, 215123, People's Republic of China

3. Suzhou Baolidi Functional Materials Research Institute, Suzhou, 215144, People's Republic of China

Abstract

An efficient Mn(iii)-promoted cascade reaction of tryptamine-derived isocyanides with arylboronic acids for accessing spiroindoline derivatives is described.

Funder

Natural Science Foundation of Jiangsu Province

Priority Academic Program Development of Jiangsu Higher Education Institutions

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/QO/D2QO01992B

Reference45 articles.

1. Catalytic asymmetric dearomatization (CADA) reaction-enabled total synthesis of indole-based natural products