Hexafluoroacetone and methyl trifluoropyruvate as precursors of modified esters of N-acyl-N-phenyl-?-amino acids

Autor:	N. D. Chkanikov, V. Yu. Tyutin, A. V. Fokin, A. F. Kolomiets, V. D. Sviridov, A. E. Zelenin
Rok vydání:	1992
Předmět:	Acylation chemistry.chemical_classification Hexafluoroacetone chemistry.chemical_compound chemistry fungi Automotive Engineering Organic chemistry General Chemistry Fungus Diseases Amino acid
Zdroj:	Bulletin of the Russian Academy of Sciences Division of Chemical Science. 41:1415-1424
ISSN:	1573-9171 1063-5211
DOI:	10.1007/bf00864339
Popis:	The C-oxyalkylation of N-aryl-α-amino acids by hexafluoroacetone (1) and methyl trifluoropyruvate (2), followed by acylation of the products3–13, 15, and17 formed, was carried out. The activity of the synthesized anilides against pathogens of plant fungus diseases was studied.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::4c23bf06946c84b62ac9cb5586cde30a https://doi.org/10.1007/bf00864339 Zobrazit plný text záznamu Full text from SpringerLink