Unexpected Electronic Behavior of Organic Azide and Metal‐Carbyne in Their 1, 3‐Dipolar Cycloaddition Reaction-Reference-Cited by-同舟云学术

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Unexpected Electronic Behavior of Organic Azide and Metal‐Carbyne in Their 1, 3‐Dipolar Cycloaddition Reaction

Published:2020-09-24 Issue:12 Volume:38 Page:1565-1570
ISSN:1001-604X
Container-title:Chinese Journal of Chemistry
language:en
Short-container-title:Chin. J. Chem.

Author:

Zhang Jing‐Xuan¹,Sheong Fu Kit¹²,Lu Zhengyu³,Zhang Hong³,Lin Zhenyang¹

Affiliation:

1. Department of Chemistry, The Hong Kong University of Science and Technology Clear Water Bay Hong Kong, China

2. Institute for Advanced Study, The Hong Kong University of Science and Technology, Clear Water Bay Hong Kong, China

3. College of Chemistry and Chemical Engineering, Xiamen University Xiamen Fujian 361005 China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cjoc.202000216

Reference38 articles.

1. 1,3‐Dipolar Cycloadditions;Huisgen R.;Proc. Chem. Soc.,1961

2. The Huisgen Reaction: Milestones of the 1,3‐Dipolar Cycloaddition

3. A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes

4. The copper(I)-catalyzed alkyne-azide cycloaddition (CuAAC) “click” reaction and its applications. An overview

5. Access to tetracyclic aromatics with bridgehead metals via metalla-click reactions

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