Beiträge zur Synthese von Cystinpeptiden, dargestellt am Beispiel der Totalsynthese von Humaninsulin* / Contributions to the Synthesis of Cystine Peptides Illustrated by the Total Synthesis of Human Insulin
Open Access
- 1 April 1981
- journal article
- research article
- Published by Walter de Gruyter GmbH in Zeitschrift für Naturforschung B
- Vol. 36 (4) , 508-514
- https://doi.org/10.1515/znb-1981-0422
Abstract
The formation of disulfide bonds in separate chemical steps in a cystine peptide containing several cystine residues is exemplified by human insulin synthesis. The synthetic methods which made this approach feasible were the thiol-induced fragmentation of sulfenyl thiocarbonate derivatives and the conversion of S-trityl- and S-acetamidomethyl cysteine peptides to cystine peptides by oxidation with iodine.This publication has 4 references indexed in Scilit:
- The Synthesis of Cystine Peptides by Iodine Oxidation of S‐Trityl‐cysteine and S‐Acetamidomethyl‐cysteine PeptidesHelvetica Chimica Acta, 1980
- Totalsynthese von Humaninsulin. IV. Beschreibung der EndstufenHelvetica Chimica Acta, 1977
- Synthese von Humaninsulin. III. Aufbau des geschützten zweikettigen Fragments A(14‐21) ‐ B(17‐30)Helvetica Chimica Acta, 1976
- Synthese von Humaninsulin. II. Aufbau des cyclischen Fragments A(1–13)Helvetica Chimica Acta, 1976