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 | Tokyo Chemical Industry Co., Ltd.(APAC)
Catalytic radical generation of π-allylpalladium complexes | Nature Catalysis
Tsuji-Trost Reaction (Pi-allyl Palladium Complex) - YouTube
Tsuji–Trost reaction - Wikipedia
Synthesis, characterization, and reactivity of (π-allyl)palladium(II) wrap-around complexes with 1,3-dienes - ScienceDirect
Palladium‐Catalyzed Electrophilic Allylation Reactions via Bis(allyl) palladium Complexes and Related Intermediates - Szabó - 2004 - Chemistry – A European Journal - Wiley Online Library
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
Mechanism of allyl deprotection through catalytic palladium π-allyl... | Download Scientific Diagram
Tsuji-Trost Reaction
Iridium-catalyzed allylic alkylations - Organic Reactions Wiki
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
Synthesis and characterization of (π-allyl)palladium(II) complexes containing dialkylbiaryl phosphine ligands - ScienceDirect
Allylpalladium chloride dimer - Wikipedia
Introduction
π-Allyl)palladium Complexes Bearing Diphosphinidenecyclobutene Ligands (DPCB): Highly Active Catalysts for Direct Conversion of Allylic Alcohols | Journal of the American Chemical Society
Trimethylenemethane Palladium Catalysed Cycloaddition - Overview
Palladium-catalyzed tetraallylation of C60 with allyl chloride and allylstannane: Mechanism, regioselectivity, and enantioselectivity | Itami Organic Chemistry Laboratory, Nagoya University
Transition-metal allyl complex - Wikiwand
![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)
Tsuji-Trost Reaction
Tsuji–Trost reaction - Wikipedia
Determination of Absolute Configuration of (π‐Allyl)Palladium Complexes by NMR Spectroscopy and Stereoselective Complexation - Gogoll - 2001 - Chemistry – A European Journal - Wiley Online Library
Palladium-Catalyzed Asymmetric Allylic Alkylation/α-Iminol Rearrangement: A Facile Access to 2-Spirocyclic-Indoline Derivatives | CCS Chem
Catalytic nucleophilic 'umpoled' π-allyl reagents - Chemical Society Reviews (RSC Publishing) DOI:10.1039/C7CS00449D
