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Chromium reagents dimethylformamide

Snatzke has found that a solution prepared from chromium trioxide and dimethylformamide with a small amount of sulfuric acid has similar chemical properties as the Sarett reagent. It is useful with acid sensitive compounds and oxidation occurs at such a moderate rate that selective oxidations are often possible. Although the position allylic to a A -double bond is not attacked, the 3-hydroxy-A -system cannot be oxidized satisfactorily to the cor-... [Pg.231]

Chromium(II) sulfate is a versatile reagent for the mild reduction of a variety of bonds. Thus aqueous dimethylformamide solutions of this reagent at room temperature couple benzylic halides, reduce aliphatic monohalides to alkanes, convert vicinal dihalides to olefins, convert geminal halides to carben-oids, reduce acetylenes to /raw5-olefins, and reduce a,j3-unsatu-rated esters, acids, and nitriles to the corresponding saturated derivatives. These conditions also reduce aldehydes to alcohols. The reduction of diethyl fumarate described in this preparation illustrates the mildness of the reaction conditions for the reduction of acetylenes and o ,j8-unsaturated esters, acids, and nitriles. [Pg.52]

III. Chromium VI Reagents / 227 Chromium Vi-acetic acid / 227 Chromium Vl-acetone / 228 Chromium trioxide-pyridine complex / 229 Chromic acid-dimethylformamide / 231 Two-phase oxidations / 232... [Pg.269]


See other pages where Chromium reagents dimethylformamide is mentioned: [Pg.207]    [Pg.223]    [Pg.713]    [Pg.243]    [Pg.113]    [Pg.34]    [Pg.383]    [Pg.65]    [Pg.25]    [Pg.382]    [Pg.181]   


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Chromium reagents

Dimethylformamide

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