53560-31-9Relevant academic research and scientific papers
An efficient microwave-promoted route to (Z)-stilbenes from trans-cinnamic acids: Synthesis of combretastatin A-4 and analogues
Bazin, Marc-Antoine,Jouanne, Marie,El-Kashef, Hussein,Rault, Sylvain
scheme or table, p. 2789 - 2794 (2010/03/03)
cis-Stilbenes were synthesized from trans-cinnamic acids, involving ethylenic-bond bromination and a subsequent one-pot microwave-promoted stereoselective debrominative decarboxylation-Suzuki cross-coupling strategy. This sequence represents a useful way to prepare a variety of combretastatin A-4 derivatives.
Kumada-Corriu cross coupling route to the anti-cancer agent combretastatin A-4
Camacho-Davila, Alejandro A.
, p. 3823 - 3833 (2008/12/23)
A short and efficient synthesis of the anticancer agent combretastatin A-4 was accomplished from inexpensive starting materials using the iron-catalyzed cross-coupling of a Grignard reagent and a bromostilbene as the key step. Copyright Taylor & Francis Group, LLC.
