24265-91-6Relevant academic research and scientific papers
Synthesis of alkyloxy stilbenes by one-pot O-alkylation-Wittig and O-alkylation-Wittig-Heck reaction sequence
Patel, Krupa N.,Kamath, Bola V.,Bedekar, Ashutosh V.
, p. 80 - 84 (2013/02/21)
A new route for the synthesis of alkyloxy stilbenes from hydroxy benzaldehydes is developed by a combination of one-pot reactions. Tandem one-pot O-alkylation-Wittig and O-alkylation-Wittig-Heck reactions offer a simple access to conjugated alkyloxy stilbenes. A highly conjugated tetra(p-alkyloxystyryl)benzene was synthesized from 1,2,4,5-tetrabromobenzene involving a series of one-pot operations following the O-alkylation-Wittig-Heck scheme.
Stilbene-based anticancer agents: Resveratrol analogues active toward HL60 leukemic cells with a non-specific phase mechanism
Simoni, Daniele,Roberti, Marinella,Invidiata, Francesco Paolo,Aiello, Enrico,Aiello, Stefania,Marchetti, Paolo,Baruchello, Riccardo,Eleopra, Marco,Di Cristina, Antonietta,Grimaudo, Stefania,Gebbia, Nicola,Crosta, Lucia,Dieli, Francesco,Tolomeo, Manlio
, p. 3245 - 3248 (2007/10/03)
Several stilbenes, related to known resveratrol, have been synthesized and tested for their anticancer effect on HL60 leukemia cell line, taking particular care of the cell cycle analysis. The most potent compound was the known (Z)-3,4′,5-trimethoxystilbe
A novel type of Pd/C-catalyzed hydrogenation using a catalyst poison: Chemoselective inhibition of the hydrogenolysis for O-benzyl protective group by the addition of a nitrogen-containing base
Sajiki, Hironao,Hirota, Kosaku
, p. 13981 - 13996 (2007/10/03)
A mild and chemoselective hydrogenation method for a variety of reducible functional groups distinguishing front aliphatic and aromatic' benzyl ethers was accomplished by the addition of an appropriate nitrogen- containing base to the Pd/C-catalyzed hydrogenation system.
