Photoinduced molecular transformations. 114. An efficient synthesis of 5,7-dihydroxy-4-methylisobenzofuran-1(3H)-one, a metabolite of aspergillus flavus and a key intermediate in the synthesis of mycophenolic acid.
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概要
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An efficient new synthesis of 5,7-dihydroxy-4-methylisobenzofuran-1(3<I>H</I>)-one, a metabolite of <I>aspergillus flavus</I> and a key intermediate in the synthesis of mycophenolic acid, is reported. The new synthesis involves the preparation of 1,2-dihydro-4,6-dimethoxy-3-methylbenzocyclobuten-1-ol and a regioselective β-scission of alkoxyl radical generated from it with lead tetraacetate as the key steps.
- 公益社団法人 日本化学会の論文
著者
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Suginome Hiroshi
Organic Synthesis Division, Department of Chemical Process Engineering, Faculty of Engineering, Hokkaido University
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Kobayashi Kazuhiro
Organic Synthesis Division, Department of Chemical Process Engineering, Faculty of Engineering, Hokkaido University
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Kobayashi Kazuhiro
Organic Synthesis Division, Faculty of Engineering, Hokkaido University
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Shimizu Hideki
Organic Synthesis Division, Faculty of Engineering, Hokkaido University
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Itoh Masahito
Organic Synthesis Division, Faculty of Engineering, Hokkaido University
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- Photoinduced molecular transformations. 114. An efficient synthesis of 5,7-dihydroxy-4-methylisobenzofuran-1(3H)-one, a metabolite of aspergillus flavus and a key intermediate in the synthesis of mycophenolic acid.