Cu-catalyzed cyclization to construct indoles from N-(ortho-chloromethyl)aryl carbamates and terminal alkynes via a one-pot reaction-Reference-Cited by-同舟云学术

Cu-catalyzed cyclization to construct indoles from N-(ortho-chloromethyl)aryl carbamates and terminal alkynes via a one-pot reaction

Published:2020 Issue:34 Volume:44 Page:14477-14480
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Shi Yang¹²³⁴⁵^ORCID,Wang Gangqiang¹²³⁴⁵,Wang Hang¹²³⁴⁵,Deng Bin¹²³⁴⁵,Gao Tao¹²³⁴⁵,Wang Jian¹²³⁴⁵,Guo Haibing¹²³⁴⁵,Wu Minghu¹²³⁴⁵,Sun Shaofa¹²³⁴⁵

Affiliation:

1. Hubei Key Laboratory of Radiation Chemistry and Functional Materials

2. Non-power Nuclear Technology Collaborative Innovation Center

3. School of Nuclear Technology and Chemistry & Biology

4. Hubei University of Science and Technology

5. Xianning 437100

Abstract

In this reaction, a new strategy for the synthesis of indoles from N-(ortho-chloromethyl)aryl carbamates and terminal alkynes via Cu-catalyzed coupling–cyclization has been developed.

Funder

National College Students Innovation and Entrepreneurship Training Program

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2020/NJ/D0NJ01981J

Reference44 articles.

1. G. W. Gribble , Indole Ring Synthesis: From Natural Products to Drug Discovery , John Wiley & Sons , 2016

2. Heterocycles from cyclopropanes: applications in natural product synthesis

3. Indoles — A promising scaffold for drug development

4. Indole Alkaloids from Plants as Potential Leads for Antidepressant Drugs: A Mini Review

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