Catalytic allylic functionalization via π-allyl palladium chemistry - Organic & Biomolecular Chemistry (RSC Publishing)
π-Allylpalladium Complex | TCI AMERICA
Trimethylenemethane Palladium Catalysed Cycloaddition - Overview
Synthesis, characterization, and reactivity of (π-allyl)palladium(II) wrap-around complexes with 1,3-dienes - ScienceDirect
Allylpalladium chloride dimer - Wikipedia
Palladium‐Catalyzed Allylic Substitution at Four‐Membered‐Ring Systems: Formation of η1‐Allyl Complexes and Electrocyclic Ring Opening - Audisio - 2013 - Angewandte Chemie International Edition - Wiley Online Library
Palladium‐Catalyzed Electrophilic Allylation Reactions via Bis(allyl) palladium Complexes and Related Intermediates - Szabó - 2004 - Chemistry – A European Journal - Wiley Online Library
organic chemistry - Formation of pi-allyl Pd cation complex - Chemistry Stack Exchange
Determination of Absolute Configuration of (π‐Allyl)Palladium Complexes by NMR Spectroscopy and Stereoselective Complexation - Gogoll - 2001 - Chemistry – A European Journal - Wiley Online Library
Kinetics and Inverse Temperature Dependence of a Tsuji–Trost Reaction in Aqueous Buffer
Iridium-catalyzed allylic alkylations - Organic Reactions Wiki
Asymmetric allylic substitution by chiral palladium catalysts: Which is more reactive, major π-allyl Pd(II) species or minor π-allyl species?,Molecular Catalysis - X-MOL
Tsuji-Trost Reaction
Mechanism of allyl deprotection through catalytic palladium π-allyl... | Download Scientific Diagram
π-Allyl)palladium Complexes Bearing Diphosphinidenecyclobutene Ligands (DPCB): Highly Active Catalysts for Direct Conversion of Allylic Alcohols | Journal of the American Chemical Society
Transition-metal allyl complex - Wikiwand
The Tsuji–Trost reaction (also called the Trost allylic alkylation or allylic alkylation) is a palladium-catalysed substitution reaction involving a substrate that contains a leaving group in an allylic position. The palladium catalyst
Development of a radical strategy for the generation of... | Download Scientific Diagram
π-Allyl)palladium Complexes Bearing Diphosphinidenecyclobutene Ligands (DPCB): Highly Active Catalysts for Direct Conversion of Allylic Alcohols | Journal of the American Chemical Society
Allylpalladium(II) Chloride Dimer | 12012-95-2
![Ligand-controlled regiodivergent π-allyl palladium catalysis enables a switch between [3+2] and [3+3] cycloadditions - Chemical Communications (RSC Publishing)](https://pubs.rsc.org/en/Content/Image/GA/C9CC00611G "Ligand-controlled regiodivergent π-allyl palladium catalysis enables a switch between [3+2] and [3+3] cycloadditions - Chemical Communications (RSC Publishing)")
Ligand-controlled regiodivergent π-allyl palladium catalysis enables a switch between [3+2] and [3+3] cycloadditions - Chemical Communications (RSC Publishing)
Synthesis and characterization of (π-allyl)palladium(II) complexes containing dialkylbiaryl phosphine ligands - ScienceDirect
Tsuji-Trost Reaction
Tsuji-Trost Reaction (Pi-allyl Palladium Complex) - YouTube
