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- Dess–Martin_periodinane abstract "Dess–Martin periodinane (DMP) is a chemical reagent used to oxidize primary alcohols to aldehydes and secondary alcohols to ketones. This periodinane has several advantages over chromium- and DMSO-based oxidants that include milder conditions (room temperature, neutral pH), shorter reaction times, higher yields, simplified workups, high chemoselectivity, tolerance of sensitive functional groups, and a long shelf life. It is named after the American chemists Daniel Benjamin Dess and James Cullen Martin who developed the reagent in 1983. It is based on IBX, but due to the acetate groups attached to the central iodine atom, DMP is much more reactive than IBX and is much more soluble in organic solvents.Reaction scheme↑ ↑ ↑".
- Dess–Martin_periodinane thumbnail Dess-Martin_periodinane.svg?width=300.
- Dess–Martin_periodinane wikiPageID "1880262".
- Dess–Martin_periodinane wikiPageRevisionID "606227546".
- Dess–Martin_periodinane imagefile "Dess-Martin periodinane.svg".
- Dess–Martin_periodinane imagefile "Dess-Martin-periodinane-DFT-2009-3D-balls.png".
- Dess–Martin_periodinane imagename "Ball-and-stick model of the Dess–Martin periodinane".
- Dess–Martin_periodinane imagename "Chemical structure of the Dess–Martin periodinane".
- Dess–Martin_periodinane iupacname "111".
- Dess–Martin_periodinane iupacname "12".
- Dess–Martin_periodinane name "Dess–Martin periodinane".
- Dess–Martin_periodinane othernames "Dess–Martin periodinane".
- Dess–Martin_periodinane subject Category:Iodates.
- Dess–Martin_periodinane subject Category:Name_reactions.
- Dess–Martin_periodinane subject Category:Oxidizing_agents.
- Dess–Martin_periodinane subject Category:Periodinanes.
- Dess–Martin_periodinane type ChemicalCompound.
- Dess–Martin_periodinane type ChemicalSubstance.
- Dess–Martin_periodinane type ChemicalObject.
- Dess–Martin_periodinane type Thing.
- Dess–Martin_periodinane comment "Dess–Martin periodinane (DMP) is a chemical reagent used to oxidize primary alcohols to aldehydes and secondary alcohols to ketones. This periodinane has several advantages over chromium- and DMSO-based oxidants that include milder conditions (room temperature, neutral pH), shorter reaction times, higher yields, simplified workups, high chemoselectivity, tolerance of sensitive functional groups, and a long shelf life.".
- Dess–Martin_periodinane label "Dess-Martin-Periodinan".
- Dess–Martin_periodinane label "Dess-Martin-perjodinaan".
- Dess–Martin_periodinane label "Dess–Martin periodinane".
- Dess–Martin_periodinane label "Periodinane de Dess-Martin".
- Dess–Martin_periodinane label "デス・マーチン酸化".
- Dess–Martin_periodinane label "戴斯-马丁氧化剂".
- Dess–Martin_periodinane sameAs Dess%E2%80%93Martin_periodinane.
- Dess–Martin_periodinane sameAs Dess-Martin-Periodinan.
- Dess–Martin_periodinane sameAs Periodinane_de_Dess-Martin.
- Dess–Martin_periodinane sameAs デス・マーチン酸化.
- Dess–Martin_periodinane sameAs Dess-Martin-perjodinaan.
- Dess–Martin_periodinane sameAs Q420909.
- Dess–Martin_periodinane sameAs Q420909.
- Dess–Martin_periodinane wasDerivedFrom Dess–Martin_periodinane?oldid=606227546.
- Dess–Martin_periodinane depiction Dess-Martin_periodinane.svg.