Chem. J. Chinese Universities ›› 1990, Vol. 11 ›› Issue (9): 958.
• Articles • Previous Articles Next Articles
Huang Huamin, Zhang Jianing, Wang Jingyang
Received:
Online:
Published:
Abstract: In K2CO3-CH3COCH3-H2O system, N-acyl-a-amino acids (Ⅰa-j) were prepared by the reaction of amino acids with N-acyl thiazolidines-2-thiones and the yields were 76%~95%. The synthesis of saturated 5(4H)-oxazolones(Ⅱa-h) from Iunder mild reaction conditions in yields of 43%~84% by the use of cyanuric chloride as a condensing reagent in the presence of triethylamine was reported. Unsaturated 5(4H)-oxazolones (Ⅲa-j) were obtained from Iin the yields of 43%~93% by the aldol reaction in which Fe2SO4)3 was used as a catalyst.
Key words: N-acyl-a-amino acid, Cyanuric chloride, Saturated 5(4H)-oxazolone, Unsaturated 5(4H)-oxazolone
TrendMD:
Huang Huamin, Zhang Jianing, Wang Jingyang . A New Method foir the Synthesis of 5(4H)-Oxazolones from N-Acyl-a-Amiho Acids[J]. Chem. J. Chinese Universities, 1990, 11(9): 958.
0 / / Recommend
Add to citation manager EndNote|Ris|BibTeX
URL: http://www.cjcu.jlu.edu.cn/EN/
http://www.cjcu.jlu.edu.cn/EN/Y1990/V11/I9/958