Optimized syntheses of Fmoc azido amino acids for the preparation of azidopeptides-Reference-Cited by-同舟云学术

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Optimized syntheses of Fmoc azido amino acids for the preparation of azidopeptides

Published:2017-01-25 Issue:3 Volume:23 Page:202-214
ISSN:1075-2617
Container-title:Journal of Peptide Science
language:en
Short-container-title:J. Pept. Sci.

Author:

Pícha Jan¹,Buděšínský Miloš¹,Macháčková Kateřina¹,Collinsová Michaela¹,Jiráček Jiří¹

Affiliation:

1. Institute of Organic Chemistry and Biochemistry; Czech Academy of Sciences; v.v.i., Flemingovo nám. 2 166 10 Prague 6 Czech Republic

Funder

Medical Research Council

Akademie Věd České Republiky

Grantová Agentura České Republiky

Publisher

Wiley

Subject

Organic Chemistry,Drug Discovery,Pharmacology,Molecular Biology,Molecular Medicine,General Medicine,Biochemistry,Structural Biology

Reference71 articles.

1. Peptidotriazoles on solid phase: 1,2,3-triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides;Tornoe;J. Org. Chem.,2002

2. A stepwise Huisgen cycloaddition process: copper(I)-catalyzed regioselective ‘ligation’ of azides and terminal alkynes;Rostovtsev;Angew. Chem.-Int. Edit.,2002

3. Copper(I)-catalyzed synthesis of azoles. DFT study predicts unprecedented reactivity and intermediates;Himo;J. Am. Chem. Soc.,2005

4. Cu-I-catalyzed alkyne-azide ‘click’ cycloadditions from a mechanistic and synthetic perspective;Bock;Eur. J. Org. Chem.,2006

5. On resin side-chain cyclization of complex peptides using CuAAC;Ingale;Org. Lett.,2011

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