Diastereoselective synthesis of non-proteinogenic α-amino acids

Autor:	L. Lecointe, M. L. Roumestant, Valérie Rolland, Philippe Viallefont, J. Martine, L. Pappalardo
Rok vydání:	2000
Předmět:	Alanine chemistry.chemical_classification Stereochemistry Chemistry Alpha (ethology) Phenylalanine Protonation Stereoisomerism Alkylation Biochemistry Amino acid Endocrinology Azatyrosine Organic chemistry
Zdroj:	The Journal of Peptide Research. 55:300-307
ISSN:	1397-002X
DOI:	10.1034/j.1399-3011.2000.00681.x
Popis:	The synthesis of enantiomerically pure azatyrosine, tribromophenylalanine and trichlorophenylalanine is described, using two methods, diastereoselective alkylation and (or) diastereoselective protonation of chiral enolates.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::7e04c9a707ca9b0ff976226a1f53782d https://doi.org/10.1034/j.1399-3011.2000.00681.x Zobrazit plný text záznamu Plný text ve formátu PDF