Tripodal amine ligands for accelerating Cu-catalyzed azide–alkyne cycloaddition: efficiency and stability against oxidation and dissociation-Reference-Cited by-同舟云学术

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Tripodal amine ligands for accelerating Cu-catalyzed azide–alkyne cycloaddition: efficiency and stability against oxidation and dissociation

Published:2017 Issue:12 Volume:7 Page:2474-2485
ISSN:2044-4753
Container-title:Catalysis Science & Technology
language:en
Short-container-title:Catal. Sci. Technol.

Author:

Zhu Zhiling¹²³⁴^ORCID,Chen Haoqing¹²³⁴^ORCID,Li Siheng¹²³⁴^ORCID,Yang Xunmo¹²³⁴,Bittner Eric¹²³⁴,Cai Chengzhi¹²³⁴

Affiliation:

1. Department of Chemistry

2. University of Houston

3. Houston

4. USA

Abstract

Oligo(ethylene glycol) tethered Cu(i) ligands sacrificially protect catalysts and biomolecules from being oxidized in the CuAAC reaction.

Funder

National Science Foundation

National Institutes of Health

Publisher

Royal Society of Chemistry (RSC)

Subject

Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2017/CY/C7CY00587C

Reference87 articles.

1. Peptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides

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

3. Click Chemistry: Diverse Chemical Function from a Few Good Reactions

4. Click chemistry reactions in medicinal chemistry: Applications of the 1,3-dipolar cycloaddition between azides and alkynes

5. Click Chemistry, A Powerful Tool for Pharmaceutical Sciences

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