Reactivity of endo-3-bromocamphor with sulfur-centered nucleophiles by an electron transfer mechanism. Electrophilic behaviour of the 3-camphoryl radical
作者:Jorge G. Uranga、Ana N. Santiago
DOI:10.1039/c0ob01108h
日期:——
The photostimulated reaction of arylthiolate ions with endo-3-bromocamphor produced both reduction and substitution products. The pKa and proton affinities of the conjugated acids were found to be good indicators of the reactivity.
芳基硫醇盐离子与光合作用的光刺激反应 内-3-溴樟脑生产还原和替代产品。发现共轭酸的p K a和质子亲和力是反应性的良好指标。