1402355-07-0Relevant academic research and scientific papers
Zinc-mediated regiodiverse synthesis of vinyl bromide derivatives and their in situ palladium-catalysed cross-coupling reactions
Miersch, Anne,Kohlmeyer, Corinna,Hilt, Gerhard
, p. 3228 - 3232 (2013/12/04)
The synthesis of vinyl bromide derivatives was realised by a zinc-mediated addition of a benzylic bromide to a terminal alkyne. The geometry of the C=C bond is dependent on the amount of zinc powder applied. When 5 mol% of Zn is used, the Z-configured vinyl bromide is generated while with 150 mol% the E-geometry is obtained predominantly. In a three-component one-pot reaction, the in situ generated vinyl bromides were reacted further in a palladium-catalysed Suzuki cross-coupling reaction utilizing aromatic boronic acids to obtain trisubstituted double bonds in good overall yields. The reactions were conducted on a 5-20 mmol scale to visualise that the reactions are also capable of generating larger amounts of products. Georg Thieme Verlag Stuttgart New York.
Stereodivergent zinc-mediated three-component synthesis of tri- and tetrasubstituted alkenes
Miersch, Anne,Hilt, Gerhard
supporting information; experimental part, p. 9798 - 9801 (2012/09/07)
Zinc simple: The loading-dependent zinc-mediated addition of benzyl bromides to alkynes is the key step for the formation of vinyl bromides. In combination with a palladium-catalyzed Suzuki cross-coupling reaction with boronic acids, tri- and tetrasubstit
