Electronic effects in asymmetric hydroboration
To determine whether electronic effects are operative in asymmetric hydroboration, a series of para-substituted 2-aryl-1-propenes were prepared and reacted with four asymmetric borane reagents. A significant correlation between the electronic nature of the para-substituent and the degree of asymmetric induction was observed only for a chloroborane-ether complex, not for any of several simple alkylboranes. A quantitative analysis of the relative reactivities is also given. © 2002 Elsevier Science Ltd. All rights reserved.
Garner, C., Chiang, S., Nething, M., & Monestel, R. (2002). Electronic effects in asymmetric hydroboration. Tetrahedron Letters, 43 (46), 8339-8342. https://doi.org/10.1016/S0040-4039(02)02013-0