Solvolysis of 2-m-chlorobenzoyloxy-4-isopropyl-2h-1,4-thiazin-3-one generation of a stable carbocation
作者:M. Hojo、R. Masuda、T. Ichi、K. Yoshinaga、M. Yamada
DOI:10.1016/s0040-4039(00)85760-3
日期:1982.1
The title compound 2b undergoes nucleophilic substition reactions with exclusive aklyl-oxygen bond fission and its rate of solvolysis is highly sensitive toward change in polarity of solvents, as is shown by its highest m-value of all reported so far in logK - logk0 = mY.
独家aklyl -氧键裂变和其溶剂分解的速率的标题化合物2b经历核取代反应是朝向在溶剂中的极性变化高度敏感的,如通过所有的它的最高m值示于的logK迄今报道-稳定常数0 =我的。