Chemistry of Amino Acids. V. Studies on α-Alkyl-α-amino Acids. IX. Mild Hydrolytic Ring Cleavage of Hydantoin Derivatives
- 31 December 1967
- journal article
- research article
- Published by Pharmaceutical Society of Japan in CHEMICAL & PHARMACEUTICAL BULLETIN
- Vol. 16 (3) , 444-447
- https://doi.org/10.1248/cpb.16.444
Abstract
It was found that hydantoin nuclei(Ia[long dash]d) were easily hydrolyzed with caustic alkali to give hydantoic acid derivatives (IIIa-c) by way of 3-tosylhydantoin derivatives (IIa-d). IIIa-c were further hydrolyzed to amino acids with diluted hydrochloric acid. The hydrolysis of IId with alkali did not furnish the hydantoic acid derivative IIId but gave N-tolylsulfonyl-2-amino-2-isobutyl-4-methylvaleramide, probably due to the steric effect.This publication has 0 references indexed in Scilit: