Stereoselectivity in glycosylation by means of 2-azido-2-desoxy-D-galactopyranose derivatives and the synthesis of the determinative oligosaccharide of blood group A, type 1

Autor:	A. Ya. Khorlin, N. V. Bovin, S. E. Zurabyan
Rok vydání:	1982
Předmět:	chemistry.chemical_classification chemistry.chemical_compound Glycosylation Chemistry Stereochemistry medicine Organic chemistry DESOXY Stereoselectivity General Chemistry Oligosaccharide Chloride medicine.drug
Zdroj:	Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 31:1023-1030
ISSN:	1573-9171 0568-5230
DOI:	10.1007/bf00949960
Popis:	1. The stereoselectivity of the glycosylation of 2-azido-2-desoxy-D-galactopyranosylhalides was studied. 2. 2-Azido-3,4,6-tri-O-benzyl-2-desoxy-β-D-galactopyranosyl chloride was proposed as a new glycosylating agent for the synthesis ofα-galactosaminides.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::72352e5f17225a10e830a361f70f7f59 https://doi.org/10.1007/bf00949960 Zobrazit plný text záznamu Full text from SpringerLink