Palladium(0)-Catalyzed Ring Cleavage of Cyclobutanone Oximes Leading to Nitriles via β-Carbon Elimination
- 14 November 2000
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 122 (48) , 12049-12050
- https://doi.org/10.1021/ja005558l
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Palladium(II)-Catalyzed Oxidative Ring Cleavage of tert-Cyclobutanols under Oxygen AtmosphereJournal of the American Chemical Society, 1999
- Synthesis of Pyrrole Derivatives by the Heck-Type Cyclization of γ,δ-Unsaturated Ketone O-PentafluorobenzoyloximesChemistry Letters, 1999
- Synthesis of Doubly Unsaturated Aldehydes and Ketones by a Novel β‐DecarbopalladationAngewandte Chemie International Edition in English, 1997
- A new and synthetically useful source of iminyl radicals.Tetrahedron Letters, 1991
- Oxygenhydrogen versus nitrogenoxygen bond cleavage in the oxidative addition of oximes to [Os3(CO)10(MeCN)2]: crystal structures of the isomers [Os3H(Me2CNO)(CO)10] and [Os3(OH)(Me2CN) (CO)10]Journal of Organometallic Chemistry, 1990