tempo has been researched along with allyl-alcohol* in 2 studies
2 other study(ies) available for tempo and allyl-alcohol
Article | Year |
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A Mn(III)/TEMPO-co-mediated tandem azidation-1,2-carbon migration reaction of allylic silyl ethers.
A novel Mn(III)/TEMPO-co-mediated tandem azidation-1,2-carbon migration reaction of allylic silyl ethers with an unactivated C=C bond has been explored, generating α-aryl-alkyl β-azido ketones with an α-quaternary stereocenter. Topics: Azides; Carbon; Cyclic N-Oxides; Ethers; Ketones; Manganese; Propanols; Stereoisomerism | 2014 |
TEMPO/NaIO4-SiO2: a catalytic oxidative rearrangement of tertiary allylic alcohols to beta-substituted alpha,beta-unsaturated ketones.
The novel catalytic method for the oxidative rearrangement of tertiary allylic alcohols to beta-substituted alpha,beta-unsaturated ketones is described. TEMPO/NaIO4-SiO2 causes facile and efficient oxidative rearrangement of various acyclic substrates as well as medium-sized and macrocyclic substrates. Topics: Alkylation; Catalysis; Cyclic N-Oxides; Ketones; Molecular Structure; Oxidation-Reduction; Periodic Acid; Propanols; Silicon Dioxide | 2008 |