Autor:	Jean-Pierre Lavergne, M. L. Roumestant, Abdelrhani Elachqar, A. Ben-Tama, El Mestafa El Hadrami, A. El Hallaoui, Ph. Viallefont
Rok vydání:	2003
Předmět:	Chiral auxiliary chemistry.chemical_compound Nucleophile Chemistry Stereochemistry Organic Chemistry Clinical Biochemistry Glycine Carbohydrate Biochemistry
Zdroj:	Amino Acids. 24:423-426
ISSN:	1438-2199 0939-4451
DOI:	10.1007/s00726-002-0323-7
Popis:	α-Heterocyclic α-aminoesters were obtained in good yields by reaction of a glycine cation equivalent and different heterocyclic nucleophiles; diastereoselectivity using a carbohydrate (galactopyranose) as N-protecting group was modest.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::5032d601285a92f65923c6619dfba78b https://doi.org/10.1007/s00726-002-0323-7 Zobrazit plný text záznamu Full text from SpringerLink