Effect of the Leaving Group on the Rate and Mechanism of the Palladium‐Catalyzed Isomerization of Cyclic Allylic Benzoates in Allylic Substitutions
- 14 February 2006
- journal article
- research article
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 2006 (5) , 1185-1192
- https://doi.org/10.1002/ejoc.200500708
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- PhosphinooxazolinesA New Class of Versatile, Modular P,N-Ligands for Asymmetric CatalysisAccounts of Chemical Research, 2000
- Structure and dynamics of chiral allyl complexes of Pd(II): NMR spectroscopy and enantioselective allylic alkylationCoordination Chemistry Reviews, 1996
- Asymmetric Transition Metal-Catalyzed Allylic AlkylationsChemical Reviews, 1996
- Chiral semicorrins and related nitrogen heterocycles as ligands in asymmetric catalysisAccounts of Chemical Research, 1993
- Selectivity in palladium catalysed allylic substitutionTetrahedron: Asymmetry, 1992
- Catalytic asymmetric synthesis by means of secondary interaction between chiral ligands and substratesChemical Reviews, 1992
- Enantioselective homogeneous catalysis involving transition-metal-allyl intermediatesChemical Reviews, 1989
- Asymmetric synthesis catalyzed by chiral ferrocenylphosphine-metal complexesPublished by Walter de Gruyter GmbH ,1988
- Addition of ketone enolates to π-allylpalladlum compounds. Stereochemistry and scope of the reactionJournal of Organometallic Chemistry, 1981
- Stereocontrolled trans and cis nucleophilic attack by acetate on .pi.-allylpalladium complexes. Applications to stereoselective palladium-catalyzed 1,4-diacetoxylation of cyclic 1,3-dienesJournal of the American Chemical Society, 1981