Synthesis of 5"-deoxy-5"-fluorolividomycin B.
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概要
- 論文の詳細を見る
A masked lividomycin B derivative in which only the C-5″ hydroxyl group remains free has been prepared and treated with diethylaminosulfur trifluoride as the key step to give the title compound. A macrocyclic compound, that is, 2′,5″-carbamate was also obtained by the above reaction, and the structure was determined chemically and by the NMR-spectrum of its deblocked derivative.
- 公益社団法人 日本化学会の論文
著者
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UMEZAWA HAMAO
Institute of Microbial Chemistry
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Tsuchiya Tsutomu
Institute of Bioorganic Chemistry
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Umezawa Sumio
Institute of Bioorganic Chemistry
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Umezawa Hamao
Institute of Bioorganic Chemistry
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Torii Takahiro
Institute of Bioorganic Chemistry
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