翻訳と辞書 ・ 1,3-Benzodioxolyl-N-methylpentanamine ・ 1,3-Benzodioxolylbutanamine ・ 1,3-beta-D-glucan phosphorylase ・ 1,3-beta-galactosyl-N-acetylhexosamine phosphorylase ・ 1,3-Beta-glucan synthase ・ 1,3-beta-oligoglucan phosphorylase ・ 1,3-Bis(dicyanomethylene)squarate ・ 1,3-Bis(diphenylphosphino)propane ・ 1,3-Bisphosphoglyceric acid ・ 1,3-Butadiene ・ 1,3-Butadiene (data page) ・ 1,3-Butanediol ・ 1,3-Cycloheptadiene ・ 1,3-Cyclohexadiene ・ 1,3-DCP ・ 1,3-Dehydroadamantane ・ 1,3-Diaminopropane ・ 1,3-Diazepine ・ 1,3-Dibromopropane ・ 1,3-Dichlorobenzene ・ 1,3-Dichloropropane ・ 1,3-Dichloropropene ・ 1,3-Difluoro-2-propanol ・ 1,3-Dihydroxyanthraquinone ・ 1,3-Diisocyanatobenzene ・ 1,3-Dimethyl-2-imidazolidinone ・ 1,3-Dimethylbutylamine ・ 1,3-Dioxane ・ 1,3-Dioxetane ・ 1,3-Dioxetanedione
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1,3-Dehydroadamantane : ウィキペディア英語版 | 1,3-Dehydroadamantane
1,3-Dehydroadamantane, formally tetracyclo()decane, is an organic compound with formula C10H14, which can be obtained from adamantane by removal of two hydrogen atoms to create an internal bond. It is a polycyclic hydrocarbon, and can be viewed also as being derived from ()propellane by addition of a methylene bridge between the two larger rings. Like other small-ring propellanes, this compound is substantially strained and unstable. ==Synthesis== 1,3-Dehydroadamantane was obtained in 1969 by R. Pincock and E. Torupka, by reduction of 1,3-dibromoadamantane according to the scheme below: :
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「1,3-Dehydroadamantane」の詳細全文を読む
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