Stereospecific synthesis of cis-stilbenes from benzaldehydes and phenylacetic acids via sequential Perkin condensation and decarboxylation
-
Add time:09/24/2019 Source:sciencedirect.com
cis-Stilbenes were synthesized stereospecifically in high yields from the cuprous oxide-catalyzed decarboxylation of α-aryl-trans-cinnamic acids that were prepared from the Perkin condensation of benzaldehydes and phenylacetic acids.
We also recommend Trading Suppliers and Manufacturers of CIS-STILBENE OXIDE (cas 1689-71-0). Pls Click Website Link as below: cas 1689-71-0 suppliers
Prev:Photosolvolysis of 9-FLUORENOL (cas 1689-64-1) derivatives in aqueous solution—exploratory studies of reactivity of photogenerated 9-fluorenyl cations
Next:Induction of metallothionein synthesis by glutathione depletion after trans- and CIS-STILBENE OXIDE (cas 1689-71-0) administration in rats☆) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Catalytic activity of Mn(III) and Fe(III) complexes of meso-tetra(n-propyl)porphyrin in oxidation of olefins: Meso-alkyl substituent in comparison with the alkenyl and aryl ones09/29/2019
- Dynamics of cis-stilbene photoisomerization: the adiabatic pathway to excited trans-stilbene09/28/2019
- Stereoselective hydrolysis of cis- and trans-stilbene oxides by hepatic microsomal epoxide hydrolase10/01/2019
- Preliminary communicationA novel one-pot synthesis and preliminary biological activity evaluation of cis-restricted polyhydroxy stilbenes incorporating protocatechuic acid and cinnamic acid fragments09/27/2019
- Liquid-phase epoxidation of trans-stilbene and cis-cyclooctene over vanadium-exchanged faujasite zeolite catalysts09/26/2019
- Induction of metallothionein synthesis by glutathione depletion after trans- and CIS-STILBENE OXIDE (cas 1689-71-0) administration in rats☆09/25/2019