Asymmetric synthesis of ?-methylaminoacids by the alkylation of glycine, alanine, and phenylalanine in chiral Ni(II) complexes

Autor:	N. S. Garbalinskaya, N. I. Chernoglazova, Yu. N. Belokon, Vladimir I. Bakhmutov, V. M. Belikov
Rok vydání:	1987
Předmět:	Alanine Chromatographic separation Chemistry Stereochemistry Glycine Diastereomer Enantioselective synthesis Organic chemistry Phenylalanine General Chemistry Alkylation
Zdroj:	Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 36:2595-2601
ISSN:	1573-9171 0568-5230
DOI:	10.1007/bf00957242
Popis:	Alkylation of alanine, phenylalanine, and glycine in the Ni(II) complexes of their Schiffs bases with S-2-N-(N′-benzylpropyl)aminobenzophenone followed by Chromatographic separation of the diastereomers has given optically pure S- and R-α-methyl-α-aminoacids.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::2909ae15062dc5b52598875dcaf099a7 https://doi.org/10.1007/bf00957242 Zobrazit plný text záznamu Full text from SpringerLink