Palladium-catalyzed tetraallylation of C60 with allyl chloride and allylstannane: Mechanism, regioselectivity, and enantioselectivity | Itami Organic Chemistry Laboratory, Nagoya University
Allylpalladium(II) Chloride Dimer 12012-95-2 | TCI EUROPE N.V.
Stereochemistry of the palladium-catalyzed allylic substitution: the syn-anti dichotomy in the formation of (π-allyl)palladium complexes and their equilibration - ScienceDirect
Development of a radical strategy for the generation of... | Download Scientific Diagram
Asymmetric allylic substitution by chiral palladium catalysts: Which is more reactive, major π-allyl Pd(II) species or minor π-allyl species? - ScienceDirect
Palladium/N-heterocyclic carbene catalysed regio and diastereoselective reaction of ketones with allyl reagents via inner-sphere mechanism | Nature Communications
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
Buy Reactivity of Cationic (Pi-Allyl)Palladium(ii) Complexes with Olefins and Dienes. Book Online at Low Prices in India | Reactivity of Cationic (Pi- Allyl)Palladium(ii) Complexes with Olefins and Dienes. Reviews & Ratings - Amazon.in
Formation of pi-allyl Pd cation complex - Chemistry Stack Exchange
Tsuji–Trost reaction - Wikiwand
Tsuji-Trost Reaction
Tsuji–Trost reaction - Wikipedia
π‐Allyl)Pd Complexes Containing N‐Heterocyclic Carbene and Pseudohalogen Ligands – Synthesis, Reactivity toward Organic Isothiocyanates and Isocyanides, and Their Catalytic Activity in Suzuki–Miyaura Cross‐Couplings - Kim - 2013 - European Journal of ...
Palladium-Catalyzed Carbene Insertion into C-X Bonds
Catalytic nucleophilic 'umpoled' π-allyl reagents - Chemical Society Reviews (RSC Publishing) DOI:10.1039/C7CS00449D
Introduction
Ligand-controlled regiodivergent π-allyl palladium catalysis enables a switch between [3+2] and [3+3] cycloadditions - Chemical Communications (RSC Publishing)