Regioselective Catalytic Allylic Alkylation Directed by Removable 2-PyMe2Si Group
- 23 June 2001
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 123 (28) , 6957-6958
- https://doi.org/10.1021/ja0157346
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Palladium-Catalyzed Cross-Coupling Reaction of Alkenyldimethyl(2-pyridyl)silanes with Organic Halides: Complete Switch from the Carbometalation Pathway to the Transmetalation PathwayJournal of the American Chemical Society, 2001
- Pyridyl Group Assisted Deprotonation of a Methyl Group on Silicon: Complex Induced Proximity Effect and Novel HydroxymethylationThe Journal of Organic Chemistry, 2001
- Highly Efficient Carbopalladation Across Vinylsilane: Dual Role of the 2-PyMe2Si Group as a Directing Group and as a Phase TagJournal of the American Chemical Society, 2000
- [Bis(2-pyridyldimethylsilyl)methyl]lithium. New Reagent for the Stereoselective Synthesis of VinylsilanesOrganic Letters, 2000
- Oxidation of 2-Pyridyldimethylsilyl Group to Hydroxyl Group by H2O2/KF. Implication of Fluoride Ion Accelerated 2-Pyridyl−Silyl Bond CleavageThe Journal of Organic Chemistry, 1999
- 2-Pyridylsilyl group as a multifunctional “phase tag" for solution phase synthesisTetrahedron Letters, 1999
- Chelation-Assisted Intermolecular Hydroacylation: Direct Synthesis of Ketone from Aldehyde and 1-AlkeneThe Journal of Organic Chemistry, 1997
- Directed Regio- and Stereoselective Nickel-Catalyzed Addition of Alkyl Grignard Reagents to Allylic EthersJournal of the American Chemical Society, 1995
- Substrate-directable chemical reactionsChemical Reviews, 1993
- Palladium-catalyzed coupling of allylic acetates with aryl- and vinylstannanesThe Journal of Organic Chemistry, 1990