Mechanistic duality of indolyl 1,3-heteroatom transposition-Reference-Cited by-同舟云学术

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Mechanistic duality of indolyl 1,3-heteroatom transposition

Published:2023 Issue:28 Volume:14 Page:7688-7698
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Lee Yujin¹,Nam Yun Seung¹,Kim Soo Young¹,Ki Jeong Eun¹,Lee Hong Geun¹^ORCID

Affiliation:

1. Department of Chemistry, Seoul National University, 1, Gwanak-ro, Gwanak-gu, Seoul 08826, South Korea

Abstract

A novel mechanistic duality has been revealed from the indolyl 1,3-heteroatom transposition (IHT) of N-hydroxyindole derivatives.

Funder

National Research Foundation of Korea

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/SC/D3SC00716B

Reference111 articles.

1. Indole alkaloids in medicine

2. Rings in Drugs

3. Analysis of the Structural Diversity, Substitution Patterns, and Frequency of Nitrogen Heterocycles among U.S. FDA Approved Pharmaceuticals

4. Indole: A privileged scaffold for the design of anti-cancer agents

5. D. S.Seigler , in Plant Secondary Metabolism , Springer , 1998 , pp. 628–654

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