Efficient Syntheses and Chemistry of Indolactam-V and Its Analogs(Organic Chemistry)
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概要
- 論文の詳細を見る
The tumor promoter, indolactam-V (1a), was synthesized in 8 steps and a 15% overall yield from methyl 4-nitroindole-3-carboxylate (2). Several chemical properties of indolactam-V analogs 10a and 10b were investigated.
- 社団法人日本農芸化学会の論文
- 1989-08-23
著者
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Masuda T
Gifu Pharmaceutical Univ. Gifu
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Masuda Toshiya
Laboratory Of Organic Chemistry Faculty Of Agriculture Nagoya University
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Masuda Toshiya
Laboratories Of Cellular Signaling And Bioorganic Chemistry Faculty Of Integrated Arts And Sciences
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Goto T
Department Of Agricultural Chemistry Faculty Of Agriculture Nagoya University
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Masuda T
Laboratory Of Food Chemistry Faculty Of Science Of Living Osaka City University
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NAKATSUKA Shin-ichi
Laboratory of Organic Chemistry, Nagoya University
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Nakatsuka Shin-ichi
Laboratory Of Organic Chemistry Nagoya University
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Nakatsuka Shin-ichi
Central Research Laboratory Hitachi Ltd.
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Goto Toshio
Laboratory Of Organic Chemistry Faculty Of Agriculture Nagoya University
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