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Details for article 1 of 11 found articles
| Title: |
An Improved Synthesis of 3,4,6-Tri-O-acetyl-2-azido-2-deoxy-α-d-galactopyranosyl Bromide: A Key Component for Synthesis of Glycopeptides and Glycolipids |
| Author: |
Broddefalk, Johan Nilsson, Ulf Kihlberg, Jan |
| Appeared in: |
Journal of carbohydrate chemistry |
| Paging: | Volume 13 (1994) nr. 1 pages 129-132 |
| Year: |
1994-01-01 |
| Contents: |
Results and discussion The α-glycosidic bond between N-acetylgalactosamine and serine or threonine is one of the most important linkages between the carbohydrate and peptide parts of O-glycoproteins.1 This linkage is found in mucous glycoproteins and is also a characteristic of many serum and membrane bound glycoproteins, including proteins containing the tumour associated TN and T antigens. α-O-Glycosidically linked N-acetylgalactosamine also occurs in the blood group A determinant2 and in glycolipids such as the Forssman antigen.3 |
| Publisher: |
Taylor & Francis |
| Source file: |
Elektronische Wetenschappelijke Tijdschriften |
Details for article 1 of 11 found articles
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