Organic photochemistry. V. Dethioacetalization by photolysis in the presence of molecular oxygen.
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Photolysis (a 200 W high pressure mercury lamp) under oxygen stream of ethylene dithioacetals of 5, 6-dimethoxy-α-indanone, α-and β-indanone, α-tetralone, 5α-and 5β-cholestan-3-ones, cholest-4-en-3-one, and cyclohexanone in an appropriate solvent (nhexane, ethanol or benzene) was carried out to give the parent ketones. Ethylene dithioacetal of cholest-5-en-3-one on photolysis followed by NaBH4 reduction gave cholest-4-en-3β-o1, showing photo-induced isomerization of the double bond.
収録刊行物
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- CHEMICAL & PHARMACEUTICAL BULLETIN
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CHEMICAL & PHARMACEUTICAL BULLETIN 27 (2), 538-540, 1979
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
- 1390282679145323520
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- NII論文ID
- 110003623643
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- NII書誌ID
- AA00602100
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- COI
- 1:CAS:528:DyaE1MXktVClurk%3D
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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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- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可