Asymmetric synthesis of S-5-benzyloxytryptophan, S-?-allylglycine and S-?-(2-naphthyl)alanine

Autor:	V. M. Belikov, N. N. Suvorov, E. V. Ivanova, M. B. Saporovskaya, A. N. Popkov, N. I. Chernoglazova, Yu. N. Belokon
Rok vydání:	1988
Předmět:	Alanine chemistry.chemical_compound Schiff base chemistry 5-benzyloxytryptophan Allylglycine Stereochemistry Glycine Enantioselective synthesis Diastereomer General Chemistry Alkylation
Zdroj:	Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 37:2541-2544
ISSN:	1573-9171 0568-5230
DOI:	10.1007/bf00952636
Popis:	The synthesis of optically pure S-5-benzyloxytryptophan, S-β-(2-naphthyl)alanine, and S-α-allylglycine was carried out by alkylating glycine in the Ni(II) complex of its Schiff base with S-2-N-(N′-benzylpropyl)aminobenzophenone, followed by Chromatographic separation of the mixture of diastereomeric alkylated complexes.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::0bb89f8b72f2fbd9fc2ac5a3444bd087 https://doi.org/10.1007/bf00952636 Zobrazit plný text záznamu Full text from SpringerLink