Reaction of cyclopropylcarbene–metal complexes with nucleophiles, halogens and HX
…, L Tirado, J Zhang, N Dike, JW Herndon
文献索引:Reid, Margaret D.; Tirado, Liz; Zhang, Jianwei; Dike, Nwamara; Herndon, James W. Journal of Organometallic Chemistry, 2005 , vol. 690, # 24-25 p. 5759 - 5776
The reaction of halogens, pseudohalogens, and HX with cyclopropyl (phenylthio) carbene- chromium complexes leads to the formation of 1, 4-dihalo-1-thiophenyl-1-butene systems with a moderate-high degree of stereocontrol in the formation of the alkene. A mechanism involving electrophilic activation of the carbene complex followed by nucleophilic attack at the cyclopropane carbon has been proposed.
[Hughes, Simon; Griffiths, Gwerydd; Stirling, Charles J. M. Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1987 , p. 1253 - 1264]