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・ 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
・ 1,3-Dipolar cycloaddition
・ 1,3-dipole
・ 1,3-Dithietane
・ 1,3-Indandione
・ 1,3-Propane sultone
・ 1,3-Propanediol
・ 1,3-propanediol dehydrogenase
1,3-Propanedithiol
・ 1,3-Thiazepine
・ 1,4,2-Dithiazole
・ 1,4,6-Androstatriene-3,17-dione
・ 1,4,7-Triazacyclononane
・ 1,4,7-Trithiacyclononane
・ 1,4-a-glucan 6-a-glucosyltransferase
・ 1,4-Benzodioxine
・ 1,4-Benzoquinone
・ 1,4-beta-D-xylan synthase
・ 1,4-Butanediol
・ 1,4-Butynediol
・ 1,4-Cycloheptadiene
・ 1,4-Cyclohexadiene
・ 1,4-Cyclohexanedione


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1,3-Propanedithiol : ウィキペディア英語版
1,3-Propanedithiol

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1,3-Propanedithiol is the chemical compound with the formula HSCH2CH2CH2SH. This dithiol is a useful reagent in organic synthesis. This liquid, which is readily available commercially, has an intense stench.
==Use in organic synthesis==
1,3-Propanedithiol is mainly used for the protection of aldehydes and ketones via their reversible formation of dithianes.〔
〕 A prototypical reaction is its formation of 1,3-dithiane from formaldehyde. The reactivity of this dithiane illustrates the concept of umpolung.
The unpleasant odour of 1,3-propanedithiol has encouraged the development of alternative reagents that generate similar derivatives.

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-Propanedithiol」の詳細全文を読む



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