. 2020 Apr 24;39(14):2594–2601. doi: 10.1021/acs.organomet.0c00167

Table 1. Reductive Hydroboration of Nitriles Catalyzed by 3a^a.

Reaction conditions: 0.33 mmol substrate, 0.72 mmol HBpin (2.2 equiv), 3a (4 mol %), 1 mL of benzene.

Isolated yields as hydrochloride.

Conversion determined by ¹⁹F{¹H} NMR spectroscopy.

Table 1. Reductive Hydroboration of Nitriles Catalyzed by 3aa.