A mild reductive conversion of oximes to ketones

DP Curran, JF Brill, DM Rakiewicz

Index: Journal of Organic Chemistry, , vol. 49, p. 1654 - 1656

Full Text: HTML

Citation Number: 83

Abstract

... University of Pittsburgh, Pittsburgh, Pennsylvania 15260 Received October 28, 1983 A large number of ketone functional group equivalents are routinely employed in organic synthesis. ... (1) Recipient of a Camille and Henry Dreyfus Grant for Young Faculty in Chemistry. ... J. Org. ...

Related Articles:

Oxidation of Unactivated Primary Aliphatic Amines Catalyzed by an Electrogenerated 3, 4??Azaquinone Species: A Small??Molecule Mimic of Amine Oxidases

[Largeron, Martine; Neudorffer, Anne; Fleury, Maurice-Bernard Angewandte Chemie - International Edition, 2003 , vol. 42, # 9 p. 1026 - 1029]

Novel Synthesis, Properties, and NAD+-NADH Type Redox Ability of 1, 3-Dimethylcyclohepta [4, 5] pyrrolo [2, 3-d] pyrimidine-2, 4 (1, 3 H)-dionylium Ions Annulated …

[Journal of Organic Chemistry, , vol. 70, # 24 p. 9780 - 9788]

New Synthesis, Properties, and Oxidizing Ability of 1, 3-Dimethyl-5, 10-methanocycloundeca [4, 5] furo [2, 3-d] pyrimidin-2, 4 (1, 3 H)-dionylium Tetrafluoroborate

[Journal of Organic Chemistry, , vol. 69, # 26 p. 9184 - 9190]

The application of intramolecular radical cyclizations of acylsilanes in the regiospecific formation of cyclic silyl enol ethers

[Journal of Organic Chemistry, , vol. 66, # 26 p. 8983 - 8991]

A convenient and mild dethioacetalization method using Fe (bpy) 3 (ClO4) 33H2O.

[Chemical and Pharmaceutical Bulletin, , vol. 34, # 9 p. 3595 - 3598]

More Articles...