Arginine side-chain modification that occurs during copper-catalysed azide–alkyne click reactions resembles an advanced glycation end product-Reference-Cited by-同舟云学术

Arginine side-chain modification that occurs during copper-catalysed azide–alkyne click reactions resembles an advanced glycation end product

Published:2016 Issue:26 Volume:14 Page:6205-6211
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Conibear Anne C.¹²³⁴⁵^ORCID,Farbiarz Karine¹²³⁴⁵,Mayer Rupert L.¹²⁶⁴⁵^ORCID,Matveenko Maria¹²³⁴⁵,Kählig Hanspeter¹²⁷⁴⁵,Becker Christian F. W.¹²³⁴⁵

Affiliation:

1. University of Vienna

2. Faculty of Chemistry

3. Institute of Biological Chemistry

4. 1090 Vienna

5. Austria

6. Institute of Analytical Chemistry

7. Institute of Organic Chemistry

Abstract

An adduct of dehydroascorbate with arginine forms during copper-catalysed azide–alkyne click reactions and resembles an advanced glycation end product.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/OB/C6OB00932H

Reference43 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 impact of click chemistry on drug discovery

4. Cu-Catalyzed Azide−Alkyne Cycloaddition

5. Reliable and Efficient Procedures for the Conjugation of Biomolecules through Huisgen Azide-Alkyne Cycloadditions

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