156173-75-0Relevant academic research and scientific papers
Scope and limitations of a modified hantzsch reaction for the synthesis of oxazole-dehydroamino acid derivatives from dehydroamino acid amides
Nagaya, Akihiro,Yamagishi, Yoji,Yonezawa, Yasuchika,Akai, Shoji,Shin, Chung-Gi,Sato, Ken-Ichi
experimental part, p. 313 - 331 (2012/03/26)
A variety of oxazole derivatives that possess an α,β-unsaturated substituent at the 2-position were conveniently synthesized in good yields via a Hantzsch-type reaction between dehydroamino acid amides and β-bromopyruvate derivatives. Furthermore, oxazole
Convenient Syntheses of Thiazoles Incorporated with α-Dehydroamino Acid and Dehydropeptide Structures
Nakamura, Yutaka,Shin, Chung-gi,Umemura, Kazuyuki,Yoshimura, Juji
, p. 1005 - 1008 (2007/10/02)
The convenient syntheses of various thiazole α-dehydroamino acids, thiazole valine ethyl ester, and their dehydrodi- and tripeptides, which are important moieties and segment of micrococcin P1 and noshiheptide, macrocyclic peptide antibiotics,
