The application of an aryl hydrazine linker prevents ß-elimination side products in the SPPS of C -terminal cysteine peptides-Reference-Cited by-同舟云学术

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The application of an aryl hydrazine linker prevents ß-elimination side products in the SPPS of C -terminal cysteine peptides

Published:2010-05-07 Issue:6 Volume:16 Page:309-313
ISSN:1075-2617
Container-title:Journal of Peptide Science
language:en
Short-container-title:J. Peptide Sci.

Author:

Ni Shuaijian,Zhang Huibin,Huang Wenlong,Zhou Jinpei,Qian Hai,Chen Wei

Funder

Chinese Ministry of Education

Graduate Students' Scientific Research Program of Jiangsu Province

Publisher

Wiley

Subject

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

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/psc.1240/fullpdf

Reference19 articles.

1. Somatostatin analogues: multiple roles in cellular proliferation, neoplasia, and angiogenesis;Dasgupta;Pharmacol. Ther.,2004

2. Drugs from slugs-past, present and future perspectives of [omega]-conotoxin research;Bingham;Chem. Biol. Interact.,2010

3. Solid phase peptide synthesis utilizing 9-fluorenylmethoxycarbonyl amino acids;Fields;Int. J. Pept. Protein. Res.,1990

4. 3-(1-Piperidinyl)alanine formation during the preparation of C-terminal cysteine peptides with the Fmoc/t-Bu strategy;Lukszo;Lett. Pept. Sci.,1996

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