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The syntheses of various 1-N-(L-aspart-4-oyl)-glycosylamines and their analogs

โœ Scribed by Michio Tanaka; Ikuo Yamashina

Book ID
108308143
Publisher
Elsevier Science
Year
1973
Tongue
English
Weight
697 KB
Volume
27
Category
Article
ISSN
0008-6215

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๐Ÿ“œ SIMILAR VOLUMES

The synthesis of disaccharide-L-asparagi
The synthesis of disaccharide-L-asparagine compounds: derivatives of N-(L-aspart-4-oyl)-4-O-ฮฒ-D-galactopyranosyl-ฮฒ-D-glucopyranosylamine (lactosyl-L-asparagine), 2-acetamido-N-(L-aspart-4-oyl)-2-deoxy-4-O-ฮฒ-D-galactopyranosyl-ฮฒ-D-glucopyranosylamine (N-acetyllactosaminyl-L-asparagine), and 2-acetamido-N-(L-aspart-4-oyl)-2-deoxy-6-O-ฮฒ-D-galactopyranosyl-ฮฒ-D-glucopyranosylamine
โœ Massimiliano Spinola; Roger W. Jeanloz ๐Ÿ“‚ Article ๐Ÿ“… 1970 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 722 KB
Hydrazinolysis-N-reacetylation of glycop
Hydrazinolysis-N-reacetylation of glycopeptides and glycoproteins. Model studies using 2-acetamido-1-N-(l-aspart-4-oyl)-2-deoxy-ฮฒ-d-glucopyranosylamine
โœ Brad Bendiak; Dale A. Cumming ๐Ÿ“‚ Article ๐Ÿ“… 1985 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 729 KB

2-Acetamido-1-N-(L-aspart-4-oyl)-2-deoxy-beta-D-glucopyranosyla mine (1) was used as a model glycopeptide to study the hydrazinolysis-N-reacetylation procedure. The major, initial product was the beta-acetohydrazide derivative of 2-acetamido-2-deoxy-D-glucose (2) which gave 2-acetamido-2-deoxy-D-glu