Total Synthesis of Maturinone through a Regioselective Diels-Alder Reaction of 5-Brominated Benzofurandione
スポンサーリンク
概要
- 論文の詳細を見る
Maturinone was efficiently prepared by means of a regiocontrolled Diels-Alder reaction between 5-bromo-2-ethoxycarbonyl-3-methylbenzo[b]furan-4,7-dione 8 and penta-1,3-diene.
- 公益社団法人日本薬学会の論文
- 1997-03-15
著者
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Fillion Houda
Laboratoire De Chimie Organique Faculte De Pharmacie Universite Claude Bernard Lyon
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Fillion Houda
Laboratoire De Chimie Organique
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Fillion Houda
Laboratoire De Chimie Organique Institut Des Sciences Pharmaceutiques Et Biologiques Universite Clau
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CHERKAOUI Omar
Laboratoire de Chimie Organique, Institut des Sciences Pharmaceutiques et Biologiques, Universite Cl
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NEBOIS Pascal
Laboratoire de Chimie Organique, Institut des Sciences Pharmaceutiques et Biologiques, Universite Cl
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Cherkaoui Omar
Laboratoire De Chimie Organique Institut Des Sciences Pharmaceutiques Et Biologiques Universite Clau
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Nebois P
Univ. Claude Bernard Lyon I Lyon Cedex Fra
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Nebois Pascal
Laboratoire De Chimie Organigue Institut Des Sciences Pharmaceutiques Et Biologiques Universite Clau
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- Total Synthesis of Maturinone through a Regioselective Diels-Alder Reaction of 5-Brominated Benzofurandione
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