Cystinpeptide aus (S‐Acetamidomethyl‐cystein)‐peptiden durch Oxydation mit Jod: Die synthese von cyclo‐L‐cystin
- 20 April 1971
- journal article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 54 (3), 927-930
- https://doi.org/10.1002/hlca.19710540319
Abstract
The conversion of S‐acetamidomethyl cysteine peptides to by a reaction with iodine is described. The method is applied in the synthesis of the hitherto unknown cyclo‐L‐cystine. The structure of this compound was confirmed by molecular weight determination, NMR. and mass spectroscopy.Keywords
This publication has 6 references indexed in Scilit:
- Total synthesis of an enzyme. I. Objective and strategyJournal of the American Chemical Society, 1969
- Eine neue, einfache Methode zur Synthese von CystinpeptidenHelvetica Chimica Acta, 1968
- Simple route to sterically pure diketopiperazinesThe Journal of Organic Chemistry, 1968
- Abbreviated designation of amino acid derivatives and polypeptidesBiochimica et Biophysica Acta (BBA) - General Subjects, 1966
- Synthesen zyklischer Polypeptide. c‐Tetraglycyl und c‐Hexaglycyl. Über aktivierte Ester VIIHelvetica Chimica Acta, 1956
- Herstellung von α‐Aminosäureestern durch Alkoholyse der MethylesterHelvetica Chimica Acta, 1953