Copper promoted synthesis of substituted quinolines from benzylic azides and alkynes-Reference-Cited by-同舟云学术

Copper promoted synthesis of substituted quinolines from benzylic azides and alkynes

Published:2015 Issue:128 Volume:5 Page:106012-106018
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Luo Ching-Zong¹²³⁴,Gandeepan Parthasarathy¹²³⁴,Wu Yun-Ching¹²³⁴,Chen Wei-Chen¹²³⁴,Cheng Chien-Hong¹²³⁴

Affiliation:

1. Department of Chemistry

2. National Tsing Hua University

3. Hsinchu 30013

4. Taiwan

Abstract

A novel method for the synthesis of substituted quinolines from benzylic azides and internal alkynes using Cu(OTf)₂is described. The reaction features a broad substrate scope, high product yields and excellent regioselectivity.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA23065A

Reference40 articles.

1. Quinoline, quinazoline and acridone alkaloids

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3. Quinoline, quinazoline and acridonealkaloids

4. Quinoline as a Privileged Scaffold in Cancer Drug Discovery

5. 1,8-Naphthyridines IV. 9-Substituted N,N-dialkyl-5-(alkylamino or cycloalkylamino) [1,2,4]triazolo[4,3-a][1,8]naphthyridine-6-carboxamides, new compounds with anti-aggressive and potent anti-inflammatory activities

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