e.g. Filippa Pettersson or Cancer Res. 75(6) , 1102-12, (2015) or 10.1002/anie.201600521
Journal of organometallic chemistry
Effects of the substituents Y in reactions of compounds of the type (Me3Si) 3CSiH (C6H4Y-p) I. Evidence against the SN2 (intermediate) mechanism for methanolysis …
DB Azarian, C Eaborn, PD Lickiss
Index: Azarian, Davoud B.; Eaborn, Colin; Lickiss, Paul D. Journal of Organometallic Chemistry, 1987 , vol. 328, p. 255 - 262
Abstract The rates of methanolysis of the iodides TsiSiH (C 6 H 4 Yp) I (Y MeO, Me, H, Cl, or CF 3) in 1/1 v/v MeOH/dioxane have been shown to be increased by electron withdrawal by Y and correspondingly decreased by electron release. This is taken to imply that the methanol is covalently involved in the transition state, and thus that, contrary to an earlier suggestion, the reaction cannot have an SN 2 (intermediate) mechanism. No explanation ...