Enantioselective Dearomatization of Indoles by an Azoalkene‐Enabled (3+2) Reaction: Access to Pyrroloindolines-Reference-Cited by-同舟云学术

Enantioselective Dearomatization of Indoles by an Azoalkene‐Enabled (3+2) Reaction: Access to Pyrroloindolines

Published:2019-10-24 Issue:2 Volume:132 Page:658-662
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Mei Guang‐Jian¹,Tang Xiwen¹,Tasdan Yildiz¹,Lu Yixin¹²³^ORCID

Affiliation:

1. Department of ChemistryNational University of Singapore 3 Science Drive 3 117543 Singapore Singapore

2. Joint School of National University of Singapore and Tianjin University International Campus of Tianjin University, Binhai New City Fuzhou Fujian 359297 P. R. China

3. National University of Singapore (Suzhou) Research Institute 377 Lin Quan Street, Suzhou Industrial Park Suzhou Jiangsu 215123 P. R. China

Funder

National Research Foundation Singapore

National University of Singapore

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.201911686

Reference131 articles.

1. For selected reviews see:

2. Chemistry of the Hexahydropyrrolo[2,3-b]indoles: Configuration, Conformation, Reactivity, and Applications in Synthesis

3. Structure, Bioactivity and Synthesis of Natural Products with Hexahydropyrrolo[2,3-b]indole

4. For related reviews see:

5. Enantioselective synthesis of all-carbon quaternary stereogenic centers in acyclic systems

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