Cobalt-catalyzed cross-coupling reactions of alkyl halides with aryl Grignard reagents and their application to sequential radical cyclization/cross-coupling reactions
Reactions of alkyl halides with arylmagnesium bromides in the presence of cobalt(II)(diphosphine) complexes are discussed. Treatment of 1-bromooctane with phenylmagnesium bromide with the aid of a catalytic amount of CoCl2(dppp) [DPPP=1,3-bis(diphenylphosphino)propane] yielded octylbenzene in good yield. The reaction mechanism would include single electron transfer from an electron-rich cobalt complex
Radical Cyclization Reactions with a Zirconocene-Olefin Complex as an Efficient Single Electron Transfer Reagent
作者:Kazuya Fujita、Hideki Yorimitsu、Koichiro Oshima
DOI:10.1055/s-2002-19777
日期:——
A zirconocene-olefin complex induced reductive radical cyclization of β-haloalkyl allyl acetals in THF. This complex served as a single electrontransferreagent to promote the cyclization. Furthermore, the reaction in DME afforded tetrahydrofuranylmethylzirconium species effectively.
Development of Radical Reactions with Zirconocene Complexes as Electron Transfer Reagents
作者:Kazuya Fujita、Hideki Yorimitsu、Koichiro Oshima
DOI:10.1246/bcsj.77.1727
日期:2004.9
Moreover, the reduction could function by using a catalytic amount of Cp 2 ZrCl 2 . A zirconocene-olefin complex also induced reductive radical cyclization of 2-haloalkyl allyl ethers in THF. This complex served as a single electrontransferreagent to promote the radical cyclization. Furthermore, the cyclization reaction in DME afforded 3-tetrahydrofuranylmethylzirconium efficiently.