Reduction of 2,2,2-Trichloroethylamines with Lithium Aluminum Hydride
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概要
- 論文の詳細を見る
It has been found that the lithium aluminum hydride reduction of 2,2,2-trichloroethylamines occurs to give amines with rearranged carbon skeletons or aziridines, depending on the precise substrate structure.
- 公益社団法人日本薬学会の論文
- 1981-03-25
著者
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関屋 実
School Of Pharmaceutical Sciences University Of Shizuoka
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関屋 実
Shizuoka College of Pharmacy
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高松 正典
Shizuoka College of Pharmacy
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高松 正典
Osaka College Of Pharmacy:(present Address)pharmaceuticals Research Center Kanebo Ltd.
関連論文
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- Thermal Rearrangements of Allyl 2,2-Dichloro-, 1,2-Dichloro- and 1,2,2-Trichloro-substituted Vinyl Sulfides
- Novel Rearrangements of α-N-Alkylamido-substituted Sulfides and Sulfones
- Syntheses and Reactions of Phenylthio-and Propylthioacetylenic Compounds
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