Hayashi Sayuri, Hirano Koji, Yorimitsu Hideki, Oshima Koichiro
Department of Material Chemistry, Graduate School of Engineering, Kyoto University, Kyoto-daigaku Katsura, Nishikyo-ku, Kyoto 615-8510, Japan.
J Am Chem Soc. 2006 Feb 22;128(7):2210-1. doi: 10.1021/ja058055u.
Treatment of tertiary homoallyl alcohol with aryl halide under palladium catalysis resulted in the transfer of the allyl moiety of the homoallyl alcohol to aryl halide and yielded the corresponding cross-coupling product stereo- and regiospecifically. The transfer process includes retro-allylation, which proceeds via a conformationally regulated six-membered transition state. The retro-allylation can be regarded as a method for the stereo- and regiospecific preparation of sigma-allylpalladium.
在钯催化下,叔高烯丙醇与芳基卤化物反应,高烯丙醇的烯丙基部分转移至芳基卤化物上,立体和区域特异性地生成相应的交叉偶联产物。转移过程包括逆向烯丙基化反应,该反应通过构象调控的六元过渡态进行。逆向烯丙基化反应可视为一种立体和区域特异性制备σ-烯丙基钯的方法。