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- TSUCHIYA TAKASHI
- School of Pharmaceutical Sciences, Showa University
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- ARAI HEIHACHIRO
- School of Pharmaceutical Sciences, Showa University
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- TONAMI TATSUO
- School of Pharmaceutical Sciences, Showa University
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- IGETA HIROSHI
- School of Pharmaceutical Sciences, Showa University
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説明
3, 4, 5, 6-Tetraphenylpyridazine 1-oxide (II) was irradiated in acetone or dichloromethane with high pressure mercury lamp (200W) for 3 hr, affording tetraphenylfuran (III), dibenzoylstilbenes (IV and V), 1-(1, 2, 3-triphenylcyclopropeny1)-Δ3, 6-bicyclo [3, 2, 0]-heptadien-2-one (VI), and the deoxygenated starting material (I). 3, 4, 6-Triphenylpyridazine 1-oxide (VIII) gave triphenylfuran (IX), cis-dibenzoylstyrene (X), 3-benzoyl-1, 2-diphenyl-1-cyclopropene (XI), and the deoxygenated starting material (VII). The reaction mechanism is also discussed
収録刊行物
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- CHEMICAL & PHARMACEUTICAL BULLETIN
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CHEMICAL & PHARMACEUTICAL BULLETIN 20 (2), 300-303, 1972
公益社団法人 日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1390001204173234176
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- NII論文ID
- 130003766964
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- ISSN
- 13475223
- 00092363
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- 本文言語コード
- en
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- データソース種別
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- JaLC
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- 使用不可