The Stereochemical Dichotomy in Palladium(0)- and Nickel(0)-Catalyzed Allylic Substitution
- 13 June 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 120 (27), 6661-6672
- https://doi.org/10.1021/ja980222l
Abstract
No abstract availableKeywords
This publication has 62 references indexed in Scilit:
- Heteroatom-Directed, Palladium-Catalyzed, Regioselective Allylation: Substitution with InversionThe Journal of Organic Chemistry, 1998
- Designing a Receptor for Molecular Recognition in a Catalytic Synthetic Reaction: Allylic AlkylationAccounts of Chemical Research, 1996
- Reversal of stereochemical path in allylic alkylations promoted by palladium and molybdenum complexesOrganometallics, 1988
- New method for the classification of nucleophiles in the palladium-catalyzed substitution of allylic acetatesThe Journal of Organic Chemistry, 1987
- Stereo- and regioselective palladium-catalyzed 1,4-acetoxychlorination of 1,3-dienes. 1-Acetoxy-4-chloro-2-alkenes as versatile synthons in organic transformationsJournal of the American Chemical Society, 1985
- Asymmetric synthesis. Mechanism of asymmetric catalytic allylationJournal of the American Chemical Society, 1985
- Asymmetric synthesis. Asymmetric catalytic allylation using palladium chiral phosphine complexesJournal of the American Chemical Society, 1985
- anti-Stereospecificity in the palladium-catalysed reactions of alkenyl- or aryl-metal derivatives with allylic electrophilesJournal of the Chemical Society, Chemical Communications, 1982
- 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
- New rules of selectivity: allylic alkylations catalyzed by palladiumAccounts of Chemical Research, 1980