Synthetic Studies on Oligosaccharide of a Glycolipid from the Spermatozoa of Bivalves. VII. The Synthesis of Di-, Tri-, Tetrasaccharides Related to Glycosphingolipid
スポンサーリンク
概要
- 論文の詳細を見る
The three kinds of oligosaccharides that constitute the partial structure of lipid IV (1) were synthesized as follows. The disaccharide O-β-D-mannopyranosyl-(1→4)-D-glucopyranose (13), the trisaccharide O-α-D-mannopyranosyl-(1→3)-O-β-D-mannopyranosyl-(1→4)-D-glucopyranose (21), and the tetrasaccharide O-α-D-mannopyranosyl-(1→3)-O-[β-D-xylopyranosyl-(1→2)]-O-β-D-mannopyranosyl-(1→4)-D-glucopyranose (25) were each synthesized by stepwise condensation of suitably protected monosaccharide units. A 1,6-anhydro-D-glucopyranose derivative was used as the glycosyl acceptor, and bromide derivatives of D-mannose and D-xylose as donors.
- 社団法人日本薬学会の論文
- 1992-07-25
著者
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荻原 幸夫
Faculty of Pharmaceutical Sciences, Nagoya City University
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羽田 紀康
共立薬科大学天然医薬資源学教室
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荻原 幸夫
Faculty Of Pharmaceutical Sciences Nagoya City University
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竹田 忠紘
Faculty Of Pharmaceutical Sciences Nagoya City University
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竹田 忠紘
共立薬科大学天然医薬資源学教室
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羽田 紀康
Faculty of Pharmaceutical Sciences, Nagoya City University
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