35826-15-4Relevant academic research and scientific papers
Synthesis of (E)-prop-1-ene-1,3-diyldibenzene derivatives via direct decarboxylative coupling of α,β-unsaturated carboxylic acids with benzyl boronic acid pinacol ester
Zhu, Mingxiang,Qiu, Zhenjiang,Zhang, Yun,Du, Hongli,Li, Jingya,Zou, Dapeng,Wu, Yangjie,Wu, Yusheng
, p. 2255 - 2257 (2017)
The first copper-catalyzed cross-coupling reaction between benzyl boronic acid pinacol ester and α,β-unsaturated carboxylic acids was described. The ready availability of the starting materials and excellent E selectivity make this protocol a safe and operationally convenient strategy for the efficient synthesis of (E)-prop-1-ene-1,3-diyldibenzene derivatives.
Direct olefination of benzaldehydes into 1,3-diarylpropenes via a copper-catalyzed heterodomino Knoevenagel-decarboxylation-Csp3-H activation sequence
Zhao, Yaping,Sun, Lu,Zeng, Tieqiang,Wang, Jiayi,Peng, Yanqing,Song, Gonghua
, p. 3493 - 3498 (2014/05/20)
Copper-catalyzed direct olefination of benzaldehydes into 1,3-diarylpropenes by a novel domino Knoevenagel-decarboxylation-Csp 3-H activation sequence is reported. This method provides a concise and effective route toward the synthesis of unsymmetrical 1,3-diarylpropene derivatives. the Partner Organisations 2014.
Iron-catalyzed direct alkenylation of sp3(C-H) bonds via decarboxylation of cinnamic acids under ligand-free conditions
Yang, Hailong,Yan, Hong,Sun, Peng,Zhu, Yan,Lu, Linhua,Liu, Defu,Rong, Guangwei,Mao, Jincheng
supporting information, p. 976 - 981 (2013/07/26)
An example of highly efficient low-cost ferrocene-catalyzed decarboxylative C(sp2)-C(sp3) coupling reactions via C-H functionalization has been developed successfully. It is noteworthy that nanoparticles of Fe3O4 could be used as a reusable catalyst for 7 times in the absence of ligand.
