Efficient construction of functionalized pyrroloindolines through cascade radical cyclization/intermolecular coupling

Author:

Jiang Yonggang1,Liu Dongxiang1,Zhang Lening1,Qin Cuirong1,Li Hui1,Yang Haitao1,Walsh Patrick J.2ORCID,Yang Xiaodong1ORCID

Affiliation:

1. Key Laboratory of Medicinal Chemistry for Natural Resources, Ministry of Education, Yunnan Provincial Center for Research & Development of Natural Products, School of Pharmacy, Yunnan University, Kunming 650091, P. R. China

2. Roy and Diana Vagelos Laboratories, Penn/Merck Laboratory for High-Throughput Experimentation, Department of Chemistry, University of Pennsylvania, 231 South 34th Street, Philadelphia, Pennsylvania 19104, USA

Abstract

A novel tandem radical cyclization/intermolecular coupling between 2-azaallyl anions and indole N-aryloxy acetamides is developed, which enables the synthesis of C3a-substituted pyrroloindolines under mild conditions.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

National Science Foundation

Publisher

Royal Society of Chemistry (RSC)

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