C-glycosides III. Cyclo-additions dipolaires - 1,3 d'oxydes de nitriles et de nitrilimines. Communication préliminaire

Autor:	N. Le Hong, J. M. Chalet, C. Sebastian, Melle F. Perret, A. Jotterand, Mme J. Tronchet, Melles L. Faivre, C. Hausser, Mme S. Thorndahl-Jaccard, Jean M. J. Tronchet
Rok vydání:	1970
Předmět:	animal structures Stereochemistry Chemistry Organic Chemistry macromolecular substances Biochemistry Medicinal chemistry Catalysis Cycloaddition carbohydrates (lipids) Inorganic Chemistry Drug Discovery lipids (amino acids peptides and proteins) Physical and Theoretical Chemistry
Zdroj:	Helvetica Chimica Acta. 53:1484-1489
ISSN:	0018-019X
DOI:	10.1002/hlca.19700530631
Popis:	1.3-dipolar cycloaddition of alkenes (or alkynes) on sugars-nitriloxides and nitrilimines led respectively to 3-glycosyl-isoxazolines (or isoxazoles) and 3-glycosyl-pyrazolines (or pyrazoles). 5-glycosyl-isoxazolines were similarly prepared from arylnitriloxides and α- or ω-unsaturated sugars. These new C-glycosides are potential antiviral and anti-tumor agents.
Databáze:	OpenAIRE
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