Tandem cyclization of o-alkynylanilines with isocyanides triggered by intramolecular nucleopalladation: access to heterocyclic fused 2-aminoquinolines-Reference-Cited by-同舟云学术

Tandem cyclization of o-alkynylanilines with isocyanides triggered by intramolecular nucleopalladation: access to heterocyclic fused 2-aminoquinolines

Published:2018 Issue:50 Volume:54 Page:6855-6858
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Wu Wanqing¹²³⁴⁵^ORCID,Li Meng⁵⁶²³⁴,Zheng Jia⁵⁶²³⁴,Hu Weigao⁵⁶²³⁴,Li Chunsheng⁵⁶²³⁴,Jiang Huanfeng⁵⁶²³⁴^ORCID

Affiliation:

1. State Key Laboratory of Luminescent Materials and Devices

2. South China University of Technology

3. Guangzhou 510640

4. China

5. Key Laboratory of Functional Molecular Engineering of Guangdong Province

6. School of Chemistry and Chemical Engineering

Abstract

A novel strategy for the synthesis of heterocyclic fused 2-aminoquinolines via palladium-catalyzed tandem cyclization of o-alkynylanilines and isocyanides has been developed.

Funder

National Natural Science Foundation of China

Pearl River S and T Nova Program of Guangzhou

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2018/CC/C8CC02028K

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4. A review on anticancer potential of bioactive heterocycle quinoline

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