Thiosugars. VII. Synthesis of Methyl 2,3,5,6-Tetradeoxy-2,3,5,6-tetrathio-β-L-galactofuranoside and -a-D-Altrofuranoside
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概要
- 論文の詳細を見る
The 5,6-dimethanesulfonyl derivative (2) of methyl 2,3-di-S-benzyl-2,3-dideoxy-2,3-dithio-α-D-altrofuranoside (1) reacted with sodium ethyl xanthate to give methyl 2,3-di-S-benzyl-2,3,5,6-tetradeoxy-2,3-dithio-5,6-(thiocarbonyl) dithio-β-L-galactofuranoside (3) and -α-D-altrofuranoside (4). Reduction of 3 and 4 with liquid ammonia-metallic sodium gave methyl 2,3,5,6-tetradeoxy-2,3,5,6-tetrathio-β-L-galactofuranoside (5) and -α-D-altrofuranoside (6), respectively.
- 公益社団法人日本薬学会の論文
- 1980-01-25
著者
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渡辺 正純
Faculty Of Pharmaceutical Sciences Kyushu University:(present Address)research Division Takeda Chemi
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小嶋 正治
Faculty Of Pharmaceutical Sciences Kyusyu University
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山口 忠敏
Faculty Of Pharmaceutical Sciences Kyushu University:(present Address)department Of Hygiene Miyazaki
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小嶋 正治
Faculty Of Pharmaceutical Sciences Kyushu University
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