16424-50-3Relevant articles and documents
Catalytic Chemoselective and Stereoselective Semihydrogenation of Alkynes to E-Alkenes Using the Combination of Pd Catalyst and ZnI2
Maazaoui, Radhouan,Abderrahim, Raoudha,Chemla, Fabrice,Ferreira, Franck,Perez-Luna, Alejandro,Jackowski, Olivier
supporting information, p. 7544 - 7549 (2019/01/03)
An efficient E-selective semihydrogenation of internal alkynes was developed under low dihydrogen pressure and low reaction temperature from commercially available reagents: Cl2Pd(PPh3)2, Zn0, and ZnI2. Kinetic studies and control experiments underline the significant role of ZnI2 in this process under H2 atmosphere, establishing that the transformation involves syn-hydrogenation followed by isomerization. This simple and easy-to-handle system provides a route to E-alkenes under mild conditions.
Palladium-catalyzed hydrophenylation of alkynes with sodium tetraphenylborate under mild conditions
Zeng, Hanxiang,Hua, Ruimao
, p. 558 - 562 (2008/09/17)
(Chemical Equation Presented) In an aqueous solution of acetic acid, PdCl2(PPh3)2 showed high catalytic activity for the hydrophenylation of both terminal and internal alkynes with sodium tetraphenylborate (NaBPh4) under mild conditions, affording phenyl alkenes in moderate to excellent yields.
Cobalt(I)-catalyzed stereoselective olefination of alkylzinc reagents with aldehydes
Wang, Jin-Xian,Fu, Ying,Hu, Yulai,Wang, Kehu
, p. 1506 - 1510 (2007/10/03)
The efficient olefination from organozinc reagents with aldehydes is exploited in a new synthesis of aryl and alkyl olefins.