688773-63-9Relevant academic research and scientific papers
Palladium-catalyzed regio- and stereoselective hydrosilylation of electron-deficient alkynes
Sumida, Yuto,Kato, Tomoe,Yoshida, Suguru,Hosoya, Takamitsu
, p. 1552 - 1555 (2012/06/15)
Highly regio- and stereoselective hydrosilylation applicable to a broad range of electron-deficient alkynes has been established using palladium catalysis. The synthetic utility of the method has been demonstrated by further transformations of α-silylalke
Novel stereoselective synthesis of (Z)-α,β-unsaturated esters by hydrostannylation-Stille tandem reaction of alkynyl esters with aryl iodides
Li, Jianying,Yu, Yan,Cheng, Mingzhu,Cai, Mingzhong
, p. 637 - 639,3 (2020/07/30)
(Z)-α,β-Unsaturated esters can be stereoselectively synthesised in one pot under mild conditions and in good yields, by the hydrostannylation of alkynyl esters followed by Stille cross-coupling with aryl iodides.
Palladium-catalyzed hydroarylation of alkynes with arenediazonium salts
Cacchi, Sandro,Fabrizi, Giancarlo,Goggiamani, Antonella,Persiani, Daniela
supporting information; experimental part, p. 1597 - 1600 (2009/04/10)
The palladium-catalyzed hydroarylation of arenediazonium tetrafluoroborates with alkynes in the presence of triphenylsilane affords stereoselectively hydroarylation products in moderate to high yields. The reaction tolerates a variety of substituents including keto, ester, cyano, and nitro groups and can be performed as a one-pot procedure generating the arenediazonium salt in situ. With ethyl phenylpropynoate as the starting alkyne, the hydroarylation affords ethyl (2)-2-arylcinnamates stereo- and regioselectively.
