Safe and efficient Boc-SPPS for the synthesis of glycopeptide-α-thioesters-Reference-Cited by-同舟云学术

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Safe and efficient Boc-SPPS for the synthesis of glycopeptide-α-thioesters

Published:2014-01-06 Issue:2 Volume:20 Page:98-101
ISSN:1075-2617
Container-title:Journal of Peptide Science
language:en
Short-container-title:J. Pept. Sci.

Author:

Izumi Masayuki¹,Murakami Masumi¹,Okamoto Ryo¹,Kajihara Yasuhiro¹²

Affiliation:

1. Department of Chemistry, Graduate School of Science; Osaka University; 1-1 Machikaneyama Toyonaka Osaka 560-0043 Japan

2. Japan Science and Technology Agency (JST); ERATO, Ito Glycotrilogy Project; 2-1 Hirosawa Wako Saitama 351-0198 Japan

Publisher

Wiley

Subject

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

Reference10 articles.

1. Synthesis of proteins by native chemical ligation;Dawson;Science,1994

2. Chemoselective ligation and modification strategies for peptides and proteins;Hackenberger;Angew. Chem. Int. Ed. Engl.,2008

3. Peptide and protein thioester synthesis via N -> S acyl transfer;Kang;Org. Biomol. Chem.,2010

4. In situ neutralization in boc-chemistry solid phase peptide synthesis - Rapid, high yield assembly of difficult sequences;Schnölzer;Int. J. Pept. Res. Ther.,2007

5. Chemical synthesis of an erythropoietin glycoform containing a complex-type disialyloligosaccharide;Murakami;Angew. Chem. Int. Ed.,2012

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