trans-1-Propen - 1 - acide ylboronique, >=95 %

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

Reactant forPalladium-phosphine-catalyzed Suzuki-Miyaura coupling reactions Cu(II)-mediated Ullmann-type coupling Palladium-catalyzed Sonogashira cross-coupling Reactant for preparation ofAlkynylphenoxyacetic acids as DP₂ receptor antagonists for treatment of allergic inflammatory diseases Tetrahydrobenzothiophenes as conformationally restricted enol-mimic inhibitors of type II dehydroquinase via Paal-Knorr synthesis involving Suzuki coupling Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-mediated cyclization Stereospecific dienes via nickel-catalyzed three-component reductive coupling with alkynes and enones

Reactant for:•Palladium-phosphine-catalyzed Suzuki-Miyaura coupling reactions•Cu(II)-mediated Ullmann-type couplingReactant for preparation of:•Alkynylphenoxyacetic acids as DP2 receptor antagonists for treatment of allergic inflammatory diseases•Tetrahydrobenzothiophenes as conformationally restricted enol-mimic inhibitors of type II dehydroquinase via Paal-Knorr synthesis involving Suzuki coupling•Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-mediated cyclization•Stereospecific dienes via nickel-catalyzed three-component reductive coupling with alkynes and enones

Other Notes

Contains varying amounts of anhydride

Packaging

1, 5 g in glass bottle