Palladium-acetate catalyst for regioselective direct arylation at C2 of 3-furanyl or 3-thiophenyl acrylates with inhibition of Heck type reaction
-
Add time:07/18/2019 Source:sciencedirect.com
Pd(OAc)2/KOAc was found to be an efficient catalytic system for the direct arylation of thiophene and furan derivatives bearing an acrylate at C3. The selectivity of the reaction strongly depends on the nature of the coordinating base. Na2CO3 and Li2CO3 favours the Heck type reaction; whereas the use of KOAc or CsOAc promotes regioselective arylation at C2 of the heteroarene and inhibits the Heck type reaction. The direct arylation products were obtained in moderate to good yields using only 0.1 mol % of catalyst. Electron-withdrawing substituent on aryl bromide, such as acetyl, formyl, ester, nitrile or nitro, favours the reaction; whereas electron-donating ones are unfavourable.
We also recommend Trading Suppliers and Manufacturers of (E)-ethyl 3-(4-Methyl-2-nitrophenyl)acrylate (cas 105910-05-2). Pls Click Website Link as below: cas 105910-05-2 suppliers
Prev:Formation of mixed halogenated dibenzo-p-dioxins and dibenzofurans (PXDD/Fs)
Next:β-Isocupreidine–hexafluoroisopropyl acrylate method for asymmetric Baylis–Hillman reactions) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Chlorhexidine delivery system from titanium/polybenzyl acrylate coating: Evaluation of cytotoxicity and early bacterial adhesion07/24/2019
- On the reactivity of aromatic acrylates in free-radical copolymerization with SO2 and terpolymerization with SO2 and 1-heptene07/23/2019
- The reactivities of nuclear-substituted phenyl acrylates in radical copolymerization with methyl methacrylate07/22/2019
- The reactions of aryl acrylates under Baylis-Hillman conditions07/20/2019
- Reactive thiol-ene emulsion-templated porous polymers incorporating pentafluorophenyl acrylate07/21/2019
- β-Isocupreidine–hexafluoroisopropyl acrylate method for asymmetric Baylis–Hillman reactions07/19/2019
-
Health and Chemical more >


