Catalytic asymmetric preparation of pyrroloindolines: strategies and applications to total synthesis-Reference-Cited by-同舟云学术

Catalytic asymmetric preparation of pyrroloindolines: strategies and applications to total synthesis

Published:2021 Issue:10 Volume:50 Page:5985-6012
ISSN:0306-0012
Container-title:Chemical Society Reviews
language:en
Short-container-title:Chem. Soc. Rev.

Author:

Mei Guang-Jian¹²³⁴⁵^ORCID,Koay Wai Lean⁵⁶⁷⁸⁶^ORCID,Tan Chuan Xiang Alvin⁵⁶⁷⁸⁶,Lu Yixin⁵⁶⁷⁸⁶^ORCID

Affiliation:

1. Green Catalysis Center, and College of Chemistry

2. Zhengzhou University

3. Zhengzhou 450001

4. China

5. Department of Chemistry

6. National University of Singapore

7. Singapore

8. Graduate School for Integrative Sciences & Engineering (NGS)

Abstract

Pyrroloindolines are widely present in natural products. In this review, we summarize state-of-the-art of catalytic asymmetric synthesis of pyrroloindolines, as well as related applications to natural products total synthesis.

Funder

National Research Foundation Singapore

National Natural Science Foundation of China

Faculty of Science, National University of Singapore

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/CS/D0CS00530D

Reference139 articles.

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

3. Recent Developments in the Catalytic, Asymmetric Construction of Pyrroloindolines Bearing All-Carbon Quaternary Stereocenters

4. Flexibility versus “rigidity” of the functional architecture of AChE active center

5. Accommodation of physostigmine and its analogues by acetylcholinesterase is dominated by hydrophobic interactions

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