vicine and nitroxyl

vicine has been researched along with nitroxyl* in 1 studies

Other Studies

1 other study(ies) available for vicine and nitroxyl

Article	Year
Nitroxyl radical/PhI(OAc)2: one-pot oxidative cleavage of vicinal diols to (di)carboxylic acids. Organic letters, 2012, Oct-05, Volume: 14, Issue:19 A mild and user-friendly one-pot oxidative cleavage of vicinal diols to their corresponding (di)carboxylic acids using AZADOs and PhI(OAc)(2) is described. 1,2-Diols and 2,3-diols as well as 1,2,3-triol gave one- or two-carbon-unit-shorter carboxylic acids. Internal vicinal diols also smoothly underwent one-pot oxidative cleavage to afford the corresponding dicarboxylic acids. Cyclic vicinal diols are converted to their corresponding open-form dicarboxylic acids. Topics: Carboxylic Acids; Catalysis; Free Radicals; Glucosides; Iodobenzenes; Molecular Structure; Nitrogen Oxides; Oxidation-Reduction; Pyrimidinones	2012

Article

Year

Nitroxyl radical/PhI(OAc)2: one-pot oxidative cleavage of vicinal diols to (di)carboxylic acids.

Organic letters, 2012, Oct-05, Volume: 14, Issue:19

A mild and user-friendly one-pot oxidative cleavage of vicinal diols to their corresponding (di)carboxylic acids using AZADOs and PhI(OAc)(2) is described. 1,2-Diols and 2,3-diols as well as 1,2,3-triol gave one- or two-carbon-unit-shorter carboxylic acids. Internal vicinal diols also smoothly underwent one-pot oxidative cleavage to afford the corresponding dicarboxylic acids. Cyclic vicinal diols are converted to their corresponding open-form dicarboxylic acids.

Topics: Carboxylic Acids; Catalysis; Free Radicals; Glucosides; Iodobenzenes; Molecular Structure; Nitrogen Oxides; Oxidation-Reduction; Pyrimidinones

2012