Glycoside synthesis with anomeric 1-N-glycobiosyl-1,2,3-triazoles

Article abstract of DOI:10.1080/07328309608005667

1,3-Dipolar cycloaddition of the acetylated 1,2-trans-and 1,2-cis-cellobiosyl, -lactosyl, -maltosyl, and -melibiosyl azides with various acetylenedicarboxylic acid esters gave the corresponding 1-N-glycobiosyl-1,2,3-triazoles (1a,b,c-8a,b,c) which have been used as glycosyl donors for the synthesis of oligosaccharides (15-17) and an anthracycline type antibiotic (18).

Full text of DOI:10.1080/07328309608005667

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Journal of Carbohydrate Chemistry
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Glycoside Synthesis with Anomeric 1-N-
1
Glycobiosyl-1,2,3-triazoles
a
a
b
Csaba Pet[otilde] , Gyula Batta , Zoltán Györgydeák & Ferenc
a
Sztaricskai
a
Research Group for Antibiotics of the Hungarian Academy of
Sciences , Lajos Kossuth University of Debrecen , P.O.B. 70, H-4010,
Debrecen, Hungary
b
Department of Organic Chemistry , Lajos Kossuth University of
Debrecen , P.O.B. 20, H-4010, Debrecen, Hungary
Published online: 22 Aug 2006.
To cite this article: Csaba Pet[otilde] , Gyula Batta , Zoltán Györgydeák & Ferenc Sztaricskai (1996)
1
Glycoside Synthesis with Anomeric 1-N-Glycobiosyl-1,2,3-triazoles , Journal of Carbohydrate
Chemistry, 15:4, 465-483, DOI: 10.1080/07328309608005667
To link to this article: http://dx.doi.org/10.1080/07328309608005667
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