Indium-mediated annulation of 2-azidoaryl aldehydes with propargyl bromides to [1,2,3]triazolo[1,5-a]quinolines-Reference-Cited by-同舟云学术

Indium-mediated annulation of 2-azidoaryl aldehydes with propargyl bromides to [1,2,3]triazolo[1,5-a]quinolines

Published:2021 Issue:28 Volume:19 Page:6346-6352
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Zhang Xiaomin¹²³⁴⁵,Yang Jiali¹²³⁴⁵,Xiong Ni¹²³⁴⁵,Han Zhe⁶⁴⁵⁷,Duan Xinhua¹²³⁴⁵^ORCID,Zeng Rong¹²³⁴⁵^ORCID

Affiliation:

1. School of Chemistry

2. MOE Key Laboratory for Nonequilibrium Synthesis and Modulation of Condensed Matter

3. Xi'an Key Laboratory of Sustainable Energy Materials Chemistry

4. Xi'an Jiaotong University (XJTU)

5. Xi'an 710049

6. School of Nuclear Science and Technology

7. P. R. China

Abstract

A highly efficient synthesis of [1,2,3]triazolo[1,5-a]quinolines under mild conditions from the cascade annulation of 2-azidoaryl aldehydes with propargyl bromides.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Shaanxi Province

Xi’an Jiaotong University

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/OB/D1OB01183A

Reference76 articles.

1. Triazolopyridines 20. Hydrogenation reactions

2. The chemistry of the triazolopyridines: an update

3. The Chemistry of the [1,2,3]Triazolo[1,5-a]pyridines: An Update

4. The Chemistry of Quinolines.

5. Quinoline, quinazoline and acridone alkaloids

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