Halide inhibition of the copper-catalysed azide–alkyne cycloaddition-Reference-Cited by-同舟云学术

Halide inhibition of the copper-catalysed azide–alkyne cycloaddition

Published:2015 Issue:7 Volume:13 Page:1974-1978
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Moorman Rebekah M.¹²³⁴,Collier Matthew B.¹²³⁴,Frohock Bram H.¹²³⁴,Womble Michael D.¹²³⁴,Chalker Justin M.¹²³⁴

Affiliation:

1. The University of Tulsa

2. Department of Chemistry and Biochemistry

3. Tulsa

4. USA

Abstract

Halides are inhibitors of the copper-catalysed azide–alkyne cycloaddition. Case studies in this inhibition are presented, along with experimental measures useful in accommodating halides in this widely used reaction.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/OB/C4OB02479F

Reference28 articles.

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

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

3. The growing applications of click chemistry

4. Cu-Catalyzed Azide−Alkyne Cycloaddition

5. The Atom Economy—A Search for Synthetic Efficiency

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