80253-12-9Relevant academic research and scientific papers
Iron-promoted synthesis of substituted 1-halo-1,4-pentadienes by reaction of 1,3-diarylpropenes with ethynylbenzenes via sp3 C-H bond activation
Mo, Hanjie,Bao, Weiliang
supporting information; experimental part, p. 4856 - 4859 (2010/10/21)
(Figure Presented) An iron-promoted sp3 C-H bond activation and C-C bond formation reaction between 1,3-diarylpropenes and ethynylbenzenes was realized with BQ (benzoquinone) as an oxidant. The reaction afforded 1-halo-1,4-pentadiene derivative
A NOVEL CARBON-CARBON BOND FORMATION BY THE LEWIS ACID CATALYZED REACTION OF β-STYRYLSILANE WITH ACETAL
Hirao, Toshikazu,Kohno, Shuichiro,Enda, Jun,Ohshiro, Yoshiki,Agawa, Toshio
, p. 3633 - 3636 (2007/10/02)
Treatment of (E)- and (Z)-β-styryltrimethylsilanes with benzaldehyde diethyl acetal in the presence of Lewis acid affords selectively 1,3,5-triphenyl-(E,E)- and (E,Z)-1,4-pentadienes, respectively.
