Nippon Nōgeikagaku Kaishi
Online ISSN : 1883-6844
Print ISSN : 0002-1407
ISSN-L : 0002-1407
Synthesis of Cyclodipeptide by the N-Carboxy Amino Acid Anhydride Method
Tomoko TAKAHASHIMuneko KANEKOMasanao OYA
Author information
JOURNAL FREE ACCESS

1982 Volume 56 Issue 4 Pages 277-279

Details
Abstract
Cyclodipeptide (diketopiperazine) consisting of α-amino acids with some polar side chains was synthesized by reaction of α-amino acid benzyl ester p-toluenesulfonate with N-carboxy α-amino acid anhydrides in acetonitrile. The reaction mechanism seems to be similar to the reaction of synthesis of diketopiperazine with alkyl side chains. Tyrosine was used as an ester component without protecting the hydroxyl group.
Content from these authors
© JAPAN SOCIETY FOR BIOSCIENCE,BIOTECHNOLOGY, ANDAGROCHEMISTRY
Previous article Next article
feedback
Top