Controllable synthesis of pyrido[2,3-b]indol-4-ones or indolo[3,2-b]quinolines via formal intramolecular C(sp2)–H functionalization-Reference-Cited by-同舟云学术

Controllable synthesis of pyrido[2,3-b]indol-4-ones or indolo[3,2-b]quinolines via formal intramolecular C(sp2)–H functionalization

Published:2019 Issue:46 Volume:17 Page:9960-9965
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Song Bo¹²³⁴⁵^ORCID,Wang Mengdan¹²³⁴⁵,Xu Murong¹²³⁴⁵^ORCID,Kong Lingkai¹²³⁴⁵^ORCID,Xie Huihui¹²³⁴⁵,Wang Chengyu⁶⁷⁸⁵^ORCID,Li Yanzhong¹²³⁴⁵^ORCID

Affiliation:

1. Shanghai Key Laboratory of Green Chemistry and Chemical Processes

2. School of Chemistry and Molecular Engineering

3. East China Normal University

4. Shanghai

5. China

6. School of Chemistry and Chemical Engineering

7. Linyi University

8. Linyi

Abstract

An atom-economical Fe-catalyzed protocol for the controllable synthesis of pyrido[2,3-b]indol-4-ones or indolo[3,2-b]quinolines through C–H/N–H coupling reactions. The natural product quindolinone was conveniently prepared by this reaction.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/OB/C9OB02108F

Reference46 articles.

1. Synthesis and Functionalization of Indoles Through Palladium-catalyzed Reactions

2. Marine Indole Alkaloids: Potential New Drug Leads for the Control of Depression and Anxiety

3. Indoles in Multicomponent Processes (MCPs)

4. Constructing Iboga Alkaloids via C–H Bond Functionalization: Examination of the Direct and Catalytic Union of Heteroarenes and Isoquinuclidine Alkenes

5. Solid-Phase Synthesis of Biologically Active Benzoannelated Nitrogen Heterocycles: An Update

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