Palladium-catalyzed highly diastereoselective cascade dihalogenation of alkyne-tethered cyclohexadienones via Umpolung of palladium enolate - Chemical Communications (RSC Publishing) DOI:10.1039/C9CC07164D
Palladium-catalyzed highly diastereoselective cascade dihalogenation of alkyne-tethered cyclohexadienones via Umpolung of palladium enolate - Chemical Communications (RSC Publishing)
![Reductions of chalcones by ammonium formate/ palladium on carbon [12,13]. | Download Table](https://www.researchgate.net/profile/Wender_Silva/publication/233600118/figure/tbl1/AS:654364133830661@1533023975997/Reductions-of-chalcones-by-ammonium-formate-palladium-on-carbon-12-13.png "Reductions of chalcones by ammonium formate/ palladium on carbon [12,13]. | Download Table")
Reductions of chalcones by ammonium formate/ palladium on carbon [12,13]. | Download Table
Effective fields at Fe57 nuclei and magnetic structure of palladium-iron alloys
Chemoselective Luche-Type Reduction of α,β-Unsaturated Ketones by Magnesium Catalysis.,Organic Letters - X-MOL
Colloidal Palladium Nanoparticles with In Situ H2: Reducing System for α,β-Unsaturated Carbonyl Compounds
Palladium-catalyzed highly diastereoselective cascade dihalogenation of alkyne-tethered cyclohexadienones via Umpolung of palladium enolate - Chemical Communications (RSC Publishing) DOI:10.1039/C9CC07164D
Palladium‐Catalyzed Intramolecular ipso‐Friedel–Crafts Allylic Alkylation of Phenols via Arylative Activation of Allenes - Nemoto - 2013 - Advanced Synthesis & Catalysis - Wiley Online Library
Palladium-catalyzed asymmetric dearomative cyclization in natural product synthesis - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/D0OB00818D
Palladium‐Catalyzed Decarboxylative Asymmetric Allylic Alkylation: Development, Mechanistic Understanding and Recent Advances - James - 2019 - Advanced Synthesis & Catalysis - Wiley Online Library
Palladium-catalysed enantioselective synthesis of Ibuprofen - ScienceDirect
PDF) Palladium-catalyzed propargylic vs. allylic alkylation | Eric Bosch - Academia.edu
Extrapolation of the gold-catalyzed cycloisomerization to the palladium-catalyzed cross-coupling/cycloisomerization of acetylenic alcohols for the synthesis of polysubstituted furans: Scope and application to tandem processes - ScienceDirect
Palladium‐Catalyzed Decarboxylative Asymmetric Allylic Alkylation: Development, Mechanistic Understanding and Recent Advances - James - 2019 - Advanced Synthesis & Catalysis - Wiley Online Library
PDF) Asymmetric Allylation of Aryl Aldehydes: Studies on the Scope and Mechanism of the Palladium Catalyzed Diethylzinc Mediated Umpolung Using Phosphoramidite Ligands.
A stereoselective synthesis of digitoxin and digitoxigen mono- and bisdigitoxoside from digitoxigenin via a palladium-catalyzed glycosylation. - Abstract - Europe PMC
A stereoselective synthesis of digitoxin and digitoxigen mono- and bisdigitoxoside from digitoxigenin via a palladium-catalyzed glycosylation. - Abstract - Europe PMC
Palladium-catalyzed asymmetric dearomative cyclization in natural product synthesis - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/D0OB00818D
PDF) Synthesis of Cyclophellitol Utilizing a Palladium Chloride Mediated-Ferrier-II Rearrangement
Palladium-catalysed coupling of vinyl triflates with enynes and its application to the synthesis of 1α,25-dihydroxyvitamin D3 - ScienceDirect
Palladium-catalyzed asymmetric dearomative cyclization in natural product synthesis - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/D0OB00818D
Palladium | Syntheticnature
PDF) Palladium(0) Nanoparticles Immobilized onto Silica/Starch Composite: Sustainable Catalyst for Hydrogenations and Suzuki Coupling
Palladium | Syntheticnature
γ-Carboline AC190 analogues via palladium catalysed allene insertion stereo and regioselective 3- and 5-component cascades - ScienceDirect
Luche Reduction - an overview | ScienceDirect Topics
Palladium-catalyzed asymmetric dearomative cyclization in natural product synthesis - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/D0OB00818D
