54068-77-8Relevant articles and documents
Copper-catalyzed Z-selective semihydrogenation of alkynes with hydrosilane: A convenient approach to cis-alkenes
Wang, Guang-Hui,Bin, Huai-Yu,Sun, Miao,Chen, Shu-Wei,Liu, Ji-Hong,Zhong, Chong-Min
supporting information, p. 2175 - 2179 (2014/03/21)
A copper catalyst generated in situ from widely available copper salt and imidazolium salt in the presence of t-BuOK showed high efficiency for the semihydrogenation of a wide range of internal and terminal alkynes to their corresponding alkenes without obvious over-reduction. Functional groups, such as hydroxyl, nitro, halides, and amino, etc. were tolerated. The Z/E ratios of the obtained alkenes were generally >99%. Finally, semireduction of bulky alkynes also went smoothly.
Stereospecific Synthesis of 1,4-Dienes by Cross-Coupling of Allyl Halides with Alkenylcopper Intermediates from Alkenyldialkylboranes
Brown, Herbert C.,Campbell, James B.
, p. 550 - 552 (2007/10/02)
Alkenylcopper intermediates, generated from alkenyldialkylborane derivatives of 9-borabicyclononane (9-BBN) and dicyclohexylborane (DCB), undergo stereospecific cross-coupling with allylic halides to yield stereodefined 1,4-dienes.