Kinetics of the Reactions of Carboxonium Ions and Aldehyde Boron Trihalide Complexes with Alkenes and Allylsilanes
Kinetics of the Reactions of Carboxonium Ions and Aldehyde Boron Trihalide Complexes with Alkenes and Allylsilanes
复制标题
碳鎓离子和醛三卤化硼配合物与烯烃和烯丙基硅烷的反应动力学
DOI:
10.1021/ja00135a002
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发表时间:
1995
影响因子:
15
通讯作者:
Gorden Gorath
中科院分区:
文献类型:
--
作者:
H. Mayr;Gorden Gorath
Second order rate constants for the reactions of carboxonium ions Ar (MeO) CH+ and aldehyde—boron trihalide complexes ArCH= 0—3 with allylsilanes and alkenes have been determined in CH2CI2 solution. The relative reactivities of these electrophiles are almost independent of the nature of the-nucleophiles, and it is possible to give an averaged reactivity order. For the electrophiles PhCH= 0—BF3, PhCH= 0—BCI3, Phtp-MeOCstDCH4", and Ph (MeO) CH+, ie, for PhCHX+ with X= F3BO™, CI3BO™, p-MeOCsHt, MeO relative averaged reactivities of1: 5 x 10* 12: 1 x 104: 4 x 105 (CH2CI2,-70 C) are determined indicating that the electrophilicities of aldehyde-BHaly complexes are only 3-6 orders of magnitude smaller than those of the corresponding carboxonium ions. The-methoxy substituted benzyl cations Ar (MeO) CH+ are 3—16 times more reactive (CH2CI2, 20 C) than their phenylogous benzhydryl analogues ArCp-MeOCeH/OCH4".