Bis(dibenzylideneacetone)palladium(0),

Code: 227994-2G D2-231

Application

Bis(dibenzylideneacetone)palladium(0) (Pd(dba)2) was employed as catalyst in the following studies:Synthesis of isomeric 2-aryl-2,5-dihydrofurans, via ...


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Your Price
€138.00 2G
€169.74 inc. VAT

Application

Bis(dibenzylideneacetone)palladium(0) (Pd(dba)2) was employed as catalyst in the following studies:Synthesis of isomeric 2-aryl-2,5-dihydrofurans, via Heck coupling of aryl bromides with alkenes using neopentyl phosphine ligands. Heck reaction of benzyl trifluoroacetate and 2,3-dihydrofuran phosphoramidite ligand.Allylation of stabilized anions.Cross coupling of allyl, alkenyl and aryl halides with organostannanes.Cross coupling of vinyl halides with alkenyl zinc species.Carbonylation of alkenyl and aryl halides.Employed with cyclic thiourea ligands in an efficient aerobic oxidation of alcohols to aldehydes and ketones.

Application Guide for Palladium Catalyzed Cross-Coupling Reactions

General description

Bis(dibenzylideneacetone)palladium(0) (Pd(dba)2) is an air stable Pd0 complex. It is a reagent for the synthesis of allylic substituted cyclopentadienes. It is a homogeneous catalyst. It catalyzes the alkylation of allyl acetates by various nucleophiles under mild conditions.

Packaging

500 mg in glass bottle

2, 5, 50 g in glass bottle

formpowder
InChI keyUKSZBOKPHAQOMP-SVLSSHOZSA-N
InChI1S/2C17H14O.Pd/c2*18-17(13-11-15-7-3-1-4-8-15)14-12-16-9-5-2-6-10-16;/h2*1-14H;/b2*13-11+,14-12+;
Quality Level100
reaction suitabilityreaction type: Buchwald-Hartwig Cross Coupling Reaction, reaction type: Hiyama Coupling, reaction type: Heck Reaction, reaction type: Sonogashira Coupling, reaction type: Suzuki-Miyaura Coupling, core: palladium, reaction type: Negishi Coupling, reaction type: Stille Coupling, reagent type: catalyst
SMILES string[Pd].O=C(/C=C/c1ccccc1)C=Cc2ccccc2.O=C(/C=C/c3ccccc3)C=Cc4ccccc4
Cas Number32005-36-0
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