Acide vinylboronique pinacol ester, contient de la phénothiazine comme stabilisateur, 95 %

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

Application

Reagent used forSuzuki-Miyaura coupling reactionsMizoroki-Heck reactions (cascade reaction)Intramolecular Nozaki-Hiyama-Kishi reactionsStereoselective Cu-catalyzed γ-selective and stereospecific couplingControl of stereoselectivity and mechanistic portrait on intramolecular (4+1)-cycloaddition of dialkoxycarbenesRegio- and stereoselective synthesis of trisubstituted alkenes via gold(I)-catalyzed hydrophosphoryloxylation of haloalkynes followed by Pd-catalyzed consecutive cross-coupling reactionsAsymmetric Birch reductive alkylationReagent used in Preparation of Molecular tubes for lipid sensingEnzymatic inhibitors, antibiotics, receptor analogs, and other biologically significant compounds (including total syntheses)

Employed in a "double" Heck-Mizoroki arylation leading to β,β-diarylated vinyl boronates which react with an additional aryl halide to form Π-extended systems. This approach was used to prepare conjugated dendrimers. Also used to prepare γ-carbonyl vinyl boronates via a light-induced radical addition of xanthates.

Packaging

1, 10 g in glass bottle