tempo and allyl-alcohol

tempo has been researched along with allyl-alcohol* in 2 studies

Other Studies

2 other study(ies) available for tempo and allyl-alcohol

Article	Year
A Mn(III)/TEMPO-co-mediated tandem azidation-1,2-carbon migration reaction of allylic silyl ethers. Chemical communications (Cambridge, England), 2014, Sep-25, Volume: 50, Issue:74 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. Organic letters, 2008, Nov-06, Volume: 10, Issue:21 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

Article

Year

A Mn(III)/TEMPO-co-mediated tandem azidation-1,2-carbon migration reaction of allylic silyl ethers.

Chemical communications (Cambridge, England), 2014, Sep-25, Volume: 50, Issue:74

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.

Organic letters, 2008, Nov-06, Volume: 10, Issue:21

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