A photoinduced SET process enables the direct B− H bond activation of NHC–boranes. In
contrast to common hydrogen atom transfer (HAT) strategies, this photoinduced reaction …

We report the (S)-2, 15-Cl2-DHTP-catalyzed enantioselective conjugate addition of organic
boronic acids to β-enaminones, providing the corresponding addition products in high yields …

The enantioselective organocatalytic conjugate alkenylation of β-substituted alkenyl
benzimidazoles afforded β-stereogenic 2-alkyl benzimidazole derivatives in excellent …

Asymmetric conjugate addition of organic boronic acids to dienones was successfully
achieved by using chiral 3, 3′-disubstituted-BINOLs or hydroxytetraphenylenes as the …

Herein, we report the enantioselective conjugate addition of organic boronic acids to α, β-
unsaturated 2-acyl imidazoles using (R)-3, 3′-I2-BINOL as the catalyst. The catalytic …

Readily available potassium alkynyltrifluoroborates were used for organocatalytic
asymmetric conjugate alkynylation of β-enaminones. The interception of a modified …

Density functional theory calculations have been performed to investigate the mechanism for
the BINOL-catalyzed asymmetric homologation of alkenylboronic acids with CF3 …

A bisperfluorotoluyl–BINOL catalyzed conjugate addition of trifluoroborate salts to doubly
vinylogous esters and aldol condensation synthesized chiral δ-substituted cyclohexenones …

The chiral binaphthol-catalyzed enantioselective conjugate addition of alkenylboronic acids
and heteroarylboronic acids to cyclic N-sulfonyl ketimines is reported, providing the 1, 4 …

The (R)-3, 3′-(3, 5-(CF3) 2-C6H3) 2-BINOL-catalyzed enantioselective conjugate addition
of organic boronic acids to α, β-unsaturated 1, 1, 1-trifluoromethyl ketones affords …