954412-46-5Relevant academic research and scientific papers
One-Pot Ketone Synthesis with Alkylzinc Halides Prepared from Alkyl Halides via a Single Electron Transfer (SET) Process: New Extension of Fukuyama Ketone Synthesis
Lee, Jung Hwa,Kishi, Yoshito
supporting information, p. 7178 - 7186 (2016/07/06)
One-pot ketone synthesis has been developed with in situ activation of alkyl halides to alkylzinc halides in the presence of thioesters and Pd-catalyst. The new method provides us with a reliable option for a coupling at a late stage in a convergent synth
Iron-catalyzed cross-coupling of alkyl halides with alkenyl Grignard reagents
Guerinot, Amandine,Reymond, Sebastien,Cossy, Janine
, p. 6521 - 6524 (2008/09/16)
(Chemical Equation Presented) Cheap and safe: An iron-catalyzed cross-coupling reaction between alkyl halides and alkenyl Grignard reagents is described. This C-C bond coupling reaction is promoted by the cheap and nontoxic FeCl3 and displays good tolerance against various functional groups.
