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Periodinane information


The Dess-Martin periodinane

Periodinanes also known as λ5-iodanes are organoiodine compounds with iodine in the +5 oxidation state. These compounds are described as hypervalent because the iodine center has more than 8 valence electrons.

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Periodinane

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Periodinanes also known as λ5-iodanes are organoiodine compounds with iodine in the +5 oxidation state. These compounds are described as hypervalent because...

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Alcohol oxidation

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solution of chromium trioxide in aqueous sulfuric acid. The Dess–Martin periodinane is a mild oxidant for the conversion of alcohols to aldehydes or ketones...

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Swern oxidation

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oxidation Albright-Goldman oxidation Corey–Kim oxidation Dess–Martin periodinane oxidation Ley oxidation (TPAP oxidation) TEMPO oxidation Omura, K.; Swern...

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Pyridinium chlorochromate

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oxidations, and hypervalent iodine compounds, such as the Dess–Martin periodinane. One disadvantage to the use of PCC is its toxicity, which it shares...

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Ketone

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or a Cr(VI) compound. Milder conditions make use of the Dess–Martin periodinane or the Moffatt–Swern methods. Many other methods have been developed...

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Oppenauer oxidation

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oxidation methods such as pyridinium chlorochromate (PCC) and Dess–Martin periodinane is that secondary alcohols are oxidized much faster than primary alcohols...

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Aldehyde

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the hypervalent organoiodine compounds (i.e., IBX acid, Dess–Martin periodinane), although these often also oxidize the α position. A Lux-Flood acid...

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Iodine

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October 2017. Boeckman Jr RK, Shao P, Mullins JJ (2000). "Dess–Martin periodinane: 1,1,1-Triacetoxy-1,1-dihydro-1,2-benziodoxol-3(1H)-one" (PDF). Organic...

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List of reagents

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applications ranging from organic synthesis to cloud seeding Dess–Martin periodinane chemical reagent used to oxidize primary alcohols to aldehydes and secondary...

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James Cullen Martin

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his doctoral student Daniel Benjamin Dess, he invented the Dess–Martin periodinane that is used for selective oxidation of alcohols. He is also known for...

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List of Vanderbilt University people

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bidentate ligand and a tridentate analog, co-invented the Dess–Martin periodinane, creator of the Martin sulfurane Emil Wolfgang Menzel Jr. (Ph.D. 1958)...

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Protecting group

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Vicente Samano, Mark D. Johnson: "Nucleic acid-related compounds. 58. Periodinane oxidation, selective primary deprotection, and remarkably stereoselective...

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DMP

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memory-dependent prefetcher, part of some CPU architectures Dess–Martin periodinane, a chemical reagent used to oxidise alcohols Dot matrix printer, a type...

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Hypervalent organoiodine compounds

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and explosive, but acetylation tempers it to the stabler Dess-Martin periodinane. Aliphatic hypoiodites can be synthesized through a variant on the Williamson...

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Hypervalent molecule

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compounds are useful reagents in organic chemistry (e.g. Dess–Martin periodinane) Tetra-, penta- and hexavalent phosphorus, silicon, and sulfur compounds...

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Farinomalein

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the furanone is oxidized to 3-isopropylfuran-2,5-dione by Dess–Martin periodinane, followed by acetic acid reflux with beta-alanine. The white powdered...

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Stahl oxidation

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to be used as the terminal oxidant. Compared to chromium-, DMSO-, or periodinane-mediated oxidations, this proves safe, environmentally-friendly, practical...

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Oseltamivir total synthesis

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alcohol 8 which is subsequently oxidized to ketone 9 with Dess-Martin periodinane. Cyanophosphorylation with diethyl phosphorocyanidate (DEPC) modifies...

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Organoiodine chemistry

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Organofluorine compounds Organochlorine compounds Organobromine compounds Iodanes Periodinanes Alex G. Fallis, Pierre E. Tessier, "2-Iodoxybenzoic acid (IBX)1" Encyclopedia...

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Iodine compounds

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October 2017. Boeckman Jr RK, Shao P, Mullins JJ (2000). "Dess–Martin periodinane: 1,1,1-Triacetoxy-1,1-dihydro-1,2-benziodoxol-3(1H)-one" (PDF). Organic...

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Quinuclidone

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Oxidation of the alcohol to the ketone 6 takes place with Dess-Martin periodinane in dichloromethane. The final step to 2-quinuclidonium tetrafluoroborate...

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Kuwajima Taxol total synthesis

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allowing the oxidation of the C4 alcohol to ketone 3.8 with the Dess-Martin periodinane. Diethylaluminum cyanide reacted in a conjugate addition to the enone...

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