Electrooxidative tandem cyclization of N-propargylanilines with sulfinic acids for rapid access to 3-arylsulfonylquinoline derivatives-Reference-Cited by-同舟云学术

Electrooxidative tandem cyclization of N-propargylanilines with sulfinic acids for rapid access to 3-arylsulfonylquinoline derivatives

Published:2021 Issue:13 Volume:23 Page:4733-4740
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Liu Jie¹²³⁴⁵,Wang Min¹²³⁴⁵,Li Laiqiang¹²³⁴⁵,Wang Lei¹²³⁴⁵^ORCID

Affiliation:

1. Key Laboratory of Green and Precise Synthetic Chemistry and Applications

2. Ministry of Education

3. Department of Chemistry

4. Huaibei Normal University

5. Huaibei

Abstract

An environmentally friendly electrochemical protocol for cyclization has been developed, which offers rapid access to structurally functional 3-arylsulfonylquinoline derivatives.

Funder

Natural Science Foundation of Anhui Province

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/GC/D1GC00171J

Reference50 articles.

1. A review on anticancer potential of bioactive heterocycle quinoline

2. Synthesis and therapeutic potential of quinoline derivatives

3. Recent advances in research of natural and synthetic bioactive quinolines

4. Antiprotozoal activity of chloroquinoline based chalcones

5. Synthesis and Antibacterial Evaluation of Certain Quinolone Derivatives

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