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New tris-alkoxycarbonyl arginine derivatives for peptide synthesis.
Authors:Jan Izdebski,Tomasz Gers,Danuta Kunce,Pawe&#x   Markowski
Affiliation:Peptide Laboratory, Department of Chemistry, Warsaw University, Poland. izdebski@chem.uw.edu.pl
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.
Keywords:arginine protection  dynorphin  guanidinylation  SPPS
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