Water-soluble, stable and azide-reactive strained dialkynes for biocompatible double strain-promoted click chemistry-Reference-Cited by-同舟云学术

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Water-soluble, stable and azide-reactive strained dialkynes for biocompatible double strain-promoted click chemistry

Published:2019 Issue:34 Volume:17 Page:8014-8018
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Sharma Krishna¹²³⁴^ORCID,Strizhak Alexander V.¹²³⁴,Fowler Elaine¹²³⁴^ORCID,Wang Xuelu⁵²⁶⁴^ORCID,Xu Wenshu⁷²⁸⁴,Hatt Jensen Claus¹²³⁴,Wu Yuteng¹²³⁴,Sore Hannah F.¹²³⁴^ORCID,Lau Yu Heng⁹¹⁰¹¹¹²^ORCID,Hyvönen Marko⁵²⁶⁴^ORCID,Itzhaki Laura S.⁷²⁸⁴^ORCID,Spring David R.¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. University of Cambridge

3. Cambridge CB2 1EW

4. UK

5. Department of Biochemistry

6. Cambridge CB2 1GA

7. Department of Pharmacology

8. Cambridge CB2 1PD

9. School of Chemistry

10. Eastern Ave

11. The University of Sydney

12. Australia

Abstract

The Sondheimer dialkyne is extensively used in double strain-promoted azide–alkyne cycloadditions.

Funder

Engineering and Physical Sciences Research Council

Royal Society

Cambridge Philosophical Society

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/OB/C9OB01745C

Reference38 articles.

1. A Strain-Promoted [3 + 2] Azide−Alkyne Cycloaddition for Covalent Modification of Biomolecules in Living Systems

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

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

4. Copper toxicity, oxidative stress, and antioxidant nutrients

5. Strain-promoted double-click reaction for chemical modification of azido-biomolecules

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