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Dess–Martin periodinane (DMP) is a chemical reagent used in the Dess–Martin oxidation, oxidizing primary alcohols to aldehydes and secondary alcohols to ketones.
Dess-Martin periodinane (DMP) is a hypervalent iodine compound widely used as a mild reagent for the oxidation of primary/secondary alcohols to aldehydes/ketones; oxidation of amides into imides; the dehydrogenation of amines to nitriles, and disulfides to sulfones.
Learn about the Dess-Martin Periodinane (DMP), a hypervalent iodine compound that oxidizes alcohols to aldehydes or ketones. Find out the mechanism, literature, and related reactions of this mild and selective oxidation method.
2,2-Dimethoxypropane (DMP) is an organic compound with the formula (CH 3) 2 C(OCH 3) 2. A colorless liquid, it is the product of the condensation of acetone and methanol. DMP is used as a water scavenger in water-sensitive reactions. Upon acid-catalyzed reaction, DMP reacts quantitatively with water to form acetone and methanol.
Learn how to oxidize primary alcohols to aldehydes using DMP, a mild and selective reagent. See the mechanism, examples and nomenclature of alcohols.
Dess-Martin periodinane | C13H13IO8 | CID 159087 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.
DMP is a hypervalent iodine compound used as an oxidizing agent in organic synthesis. Learn about its name reactions, recent literature, and safety precautions.
