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Redox Mechanisms Displaying 32 mechanisms: Redox- Oxidation- alcohol to ketone using CrO3 Redox- Oxidation- alcohol to aldehyde (DCC)- Pfitzner-Moffatt oxidation Redox- Oxidation- alcohol to carbonyl- bromine water Redox- Oxidation- alcohol to carbonyl- Dess Martin Redox- Oxidation- alcohol to carbonyl- Oppenauer Redox- Oxidation- alcohol to carbonyl- Swern Oxidation Redox- Oxidation- Aldehyde to carboxylic acid using CrO3 Redox- Oxidation- alkene using Pb(OAc)4 Redox- Oxidation- alkenes to ketones (Wacker) Redox- Oxidation- alkenes using SeO2 to form allylic alcohol Redox- Oxidation- autoxidation using O2 Redox- Oxidation- formation of PCC (CrO3 equivalent) Redox- Oxidation- oxidation of alkene to alcohol and amine using osmium compund Redox- Oxidation- oxidation of alkene to alcohol and amine using Sharpless method Redox- Oxidation- oxidation of alkene to allylic alcohol using CrO3 Redox- Oxidation- oxidation of alkene to diol using OsO4 Redox- Oxidation- oxidation of alpha-hydroxy carboxylic acid to aldehyde Redox- Oxidation- oxidation of cyclohexene to cyclopentane aldehyde uisng thallium Redox- Oxidation- oxidation of diol to dialdehyde using NaIO4 Redox- Oxidation- oxidation of diol using Pb(OAc)4 Redox- Oxidation- oxidation of phenol using Fe(III) Redox- Oxidation- reaction of diol with CrO3 Redox- Oxidation- SeO2 oxidation of ketone Redox- Reduction- Birch reduction of benzene Redox- Reduction- Birch reduction- with carbonyl functional group Redox- Reduction- Diborane reduction of carboxylic acids/amides Redox- Reduction- Evans- beta hydroxy-ketone to 1,3-diol Redox- Reduction- metal ammonia reduction of alpha-beta unsaturated ketone (trans-decalin) Redox- Reduction- methylation of amines using formaldehyde and formic acid (Eschweiler-Clark) Redox- Reduction- Red-Al? reduction of alkyne Redox- Reduction- reduction of ester to ketone using DIBAL-H Redox- Reduction- reduction of ketone- Meerwein-Pondorf-Verley reaction