Literature DB >> 15635728

New tris-alkoxycarbonyl arginine derivatives for peptide synthesis.

Jan Izdebski1, Tomasz Gers, Danuta Kunce, Paweł Markowski.   

Abstract

alpha-Alkoxycarbonyl protected ornithines were treated with N,N'-[Z(2Cl)](2)-S-methylisothiourea and N,N'-[Z(2Br)](2)-S-methylisothiourea, N,N'-Z(2)-S-methylisothiourea and N,N'-Boc(2)-S-methylisothiourea to form N(alpha, omega, omega')-tris-alkoxycarbonyl arginines. Two of them, Boc-Arg-{omega,omega'-[Z(2Br)](2)}-OH and Boc-Arg-{omega,omega'-[Z(2Cl)](2)}-OH, were used for the synthesis of dermorphin fragments containing two or three arginine residues. Examination of the products by HPLC and ESI-MS revealed that the purity of the materials obtained with the use of the new derivatives was higher than that obtained in concurrent syntheses in which Boc-Arg(Tos) was used. Copyright (c) 2004 European Peptide Society and John Wiley & Sons, Ltd.

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Year:  2005        PMID: 15635728     DOI: 10.1002/psc.585

Source DB:  PubMed          Journal:  J Pept Sci        ISSN: 1075-2617            Impact factor:   1.905


  2 in total

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Authors:  Edward A Hall; Erkin Kuru; Michael S VanNieuwenhze
Journal:  Org Lett       Date:  2012-05-21       Impact factor: 6.005

2.  A modular approach to synthetic RNA binders of the hepatitis C virus internal ribosome entry site.

Authors:  Maia Carnevali; Jerod Parsons; David L Wyles; Thomas Hermann
Journal:  Chembiochem       Date:  2010-07-05       Impact factor: 3.164

  2 in total

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