Terpenoids. XXXVII. Hypoiodite Reactions with 6-Hydroxy-17-norkaurane- and 7-Norgibberellane-derivatives
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概要
- 論文の詳細を見る
On the hypoiodite reaction, 17-norkauran-6α-ols 3,5,13,17,and 22 gave 4,6,14,18,and 28,respectively. The same reactions on 7-norgibberellane derivatives, 30 and 32 afforded 31 and 33,respectively. Finally 17-norkauran-6β-ols 36,38,and 41 on the same reaction yielded 37,a mixture of 39 and 40,and 42,respectively. Thus, the O-functionalization of the inactive C-19 methyl group of 17-norkauran-6-ols was achieved by means of the hypoiodite reaction with 6β-ols.
- 公益社団法人日本薬学会の論文
- 1976-09-25
著者
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野出 学
Kyoto Pharmaceutical University
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野出 学
Institute For Chemical Research Kyoto University
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堀 均
Institute For Chemical Research Kyoto University
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藤田 栄一
京都大学化学研究所
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藤田 栄一
Osaka University Of Pharmaceutical Sciences
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藤田 栄一
Institute for Chemical Research, Kyoto University
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藤田 栄一
Institute For Chemical Research Kyoto University
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