An isocyanide insertion approach to substituted pyrrolo[2,3-b]quinolines under metal-free and azide-free conditions-Reference-Cited by-同舟云学术

An isocyanide insertion approach to substituted pyrrolo[2,3-b]quinolines under metal-free and azide-free conditions

Published:2016 Issue:10 Volume:3 Page:1299-1303
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Liu Cheng-Guo¹²³⁴⁵,Gu Zheng-Yang¹²³⁴⁵,Bai Hui-Wen¹²³⁴⁵,Wang Shun-Yi¹²³⁴⁵,Ji Shun-Jun¹²³⁴⁵

Affiliation:

1. Key Laboratory of Organic Synthesis of Jiangsu Province

2. College of Chemistry

3. Chemical Engineering and Materials Science & Collaborative Innovation Center of Suzhou Nano Science and Technology

4. Soochow University

5. Suzhou

Abstract

An isocyanide insertion approach to construct the pyrrolo[2,3-b]quinoline skeleton by an I₂/CHP mediated reaction of aminome-thylenecyclo-propanes (amino-MCPs) is developed.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/QO/C6QO00373G

Reference67 articles.

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5. A facile synthesis of pyrrolo[2,3-b]quinolines via a Rh(i)-catalyzed carbodiimide-Pauson–Khand-type reaction

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