Synthesis of 3,3′-bisindoles <i>via</i> demethylenation-Reference-Cited by-同舟云学术

Synthesis of 3,3′-bisindoles via demethylenation

Published:2022 Issue:19 Volume:9 Page:5281-5284
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Chen Hui¹,Cui Ranran¹,Zhang Yahui¹,Gao Yu¹^ORCID,Chen Haijun¹^ORCID

Affiliation:

1. Key Laboratory of Molecule Synthesis and Function Discovery (Fujian Province University), College of Chemistry, Fuzhou University, Fuzhou, Fujian 350116, China

Abstract

This work provides a mild demethylenation for the synthesis of 3,3′-bisindoles.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/QO/D2QO01010K

Reference29 articles.

1. A Mild and Efficient CH2-Extrusion Reaction for the Enantiospecific Synthesis of Highly Configurationally Stable Tröger Bases

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3. RhIII-Catalyzed Synthesis of Cyclopenta[b]carbazoles via Cascade C–H/C–C Bond Cleavage and Cyclization Reactions: Using Amide as a Traceless Directing Group

4. Transition-Metal-Free Tandem Oxidative Removal of Benzylic Methylene Group by C–C and C–N Bond Cleavage Followed by Intramolecular New Aryl C–N Bond Formation under Radical Conditions

5. Transition-Metal-Free Aerobic Oxidative Cleavage of CC Bonds in α-Hydroxy Ketones and Mechanistic Insight to the Reaction Pathway

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