18435-37-5Relevant articles and documents
Convenient Synthesis of Diene-Zirconocenes and Regioselective Partial Reduction of the More Highly Substituted Double Bonds of Conjugated Dienes via Complexation with Zirconocenes and Protonolysis
Maye, John P.,Negishi, Ei-ichi
, p. 1830 - 1831 (1993)
Conjugated dienes can be initially converted to their zirconocene complexes most conveniently by their reaction with (C5H5)2ZrCl2 and freshly ground Mg; the resultant complexes can then be protonolysed with 3 mol dm-3 HCl to give regioselectively monoenes corresponding to partial hydrogenation of the more highly substituted double bond.
Ni-catalyzed alkylative dimerization of vinyl Grignard reagents using alkyl fluorides
Terao, Jun,Watabe, Hiroyasu,Kambe, Nobuaki
, p. 3656 - 3657 (2007/10/03)
Alkyl halides underwent unique cross-coupling reaction with vinylmagnesium chloride in the presence of Ni catalyst to give 2-alkyl-3-butenyl Grignard reagent (1) in high yields. This reaction proceeded efficiently at 25 °C in THF using primary and seconda