Regioselective synthesis of 3-nitroindoles under non-acidic and non-metallic conditions-Reference-Cited by-同舟云学术

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Regioselective synthesis of 3-nitroindoles under non-acidic and non-metallic conditions

Published:2023 Issue:38 Volume:13 Page:26581-26586
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Zhang Hua¹²^ORCID,Su Rong-Chuan¹²^ORCID,Qin Yu-Li¹²,Wang Xiao-Juan³,Chen Dan¹²,Liu Xiao-Rong¹²,Jiang Yu-Xin¹²,Zhao Peng¹²^ORCID

Affiliation:

1. Department of Pharmacology, North Sichuan Medical College, Nanchong 637100, China

2. Institute of Materia Medica of North Sichuan Medical College, China

3. Department of Innovation & Entrepreneurship of NSMC, China

Abstract

An electrophilic substitution reaction, without acid and metal, of indole with ammonium tetramethylnitrate for accessing 3-nitroindole has been developed.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/RA/D3RA03193D

Reference67 articles.

1. Indole, a Privileged Structural Core Motif

2. Indole-based allosteric inhibitors of HIV-1 integrase

3. A review on recent developments of indole-containing antiviral agents

4. Palladium(0)-Catalyzed Dearomative [3 + 2] Cycloaddition of 3-Nitroindoles with Vinylcyclopropanes: An Entry to Stereodefined 2,3-Fused Cyclopentannulated Indoline Derivatives

5. Enantioselective Formal [4+2] Cycloadditions to 3-Nitroindoles by Trienamine Catalysis: Synthesis of Chiral Dihydrocarbazoles

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