Alkali ion-controlled chemoselective indolation of allylic alcohols by base catalysis-Reference-Cited by-同舟云学术

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Alkali ion-controlled chemoselective indolation of allylic alcohols by base catalysis

Published:2024 Issue:17 Volume:11 Page:4794-4804
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Wang Ning¹²,Chen Ruzhao¹,Chen Zhe²,Li Weikang²^ORCID,Wen Xiuling³,Zhao Cunyuan¹,Ke Zhuofeng¹²^ORCID

Affiliation:

1. School of Chemistry, PCFM Lab, Sun Yat-sen University, Guangzhou 510275, China

2. School of Materials Science and Engineering, the Key Laboratory of Low-carbon Chemistry & Energy Conservation of Guangdong Province, Sun Yat-sen University, Guangzhou 510275, China

3. Health College of Traditional Chinese Medicine, Guangzhou Nanfang University, Guangzhou 510970, China

Abstract

A highly efficient, and transition-metal-free base-mediated catalytic system for selective indolation of allylic alcohols tuned by an alkali metal ion.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D4QO00777H

Reference81 articles.

1. Indole based cyclooxygenase inhibitors: Synthesis, biological evaluation, docking and NMR screening

2. Indoles as therapeutics of interest in medicinal chemistry: Bird's eye view

3. Mushroom-Derived Indole Alkaloids

4. Chemical Evolution of Natural Product Structure

5. Discovery of 4-[3-(trans-3-Dimethylaminocyclobutyl)-1H-indol-5-ylmethyl]- (4S)-oxazolidin-2-one (4991W93), a 5HT1B/1D Receptor Partial Agonist and a Potent Inhibitor of Electrically Induced Plasma Extravasation

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