Investigation of new methods for the synthesis of C–C bonds is fundamental for the
development of new organic drugs and materials. Aryl-, alkenyl-and alkynylboronic acids …

Organocatalysis has emerged as a powerful synthetic tool in organic chemistry in the last
few decades. Among various classes of organocatalysis, chiral diol-based scaffolds, such as …

Structurally, boronic acids are trivalent boron-containing organic compounds that possess
one alkyl substituent (ie, a C–B bond) and two hydroxyl groups to fill the remaining valences …

Carbohydrate-Catalyzed Enantioselective Alkene Diboration: Enhanced Reactivity of 1,2-Bonded
Diboron Complexes | Journal of the American Chemical Society ACS ACS Publications C&EN …

Bis‐heteroaryl or bis‐aryl stereocenters were formed by an organocatalytic enantioselective
conjugate addition using the respective trifluoroborate salts as nucleophiles. Control studies …

Catalytic enantioselective functionalization of unactivated 1, 1‐disubstituted alkenes is
challenging due to the difficulty to discriminate the enantiotopic faces. Enantioselective …

Bismuth-catalyzed allylation of para -quinone methides - Chemical Communications (RSC
Publishing) DOI:10.1039/C6CC06605D Royal Society of Chemistry View PDF VersionPrevious …

The enantioselective formation of stereocenters proximal to unprotected heterocycles has
been accomplished. Thus, vinyl boronic acids are added to heterocycle-appended enones …

(S)-2, 15-Br2-DHTP-catalyzed asymmetric conjugate addition of boronic acids to β-
trifluoromethyl α, β-unsaturated ketones and enones was studied. The reaction afforded the …

The Suzuki reaction, which couples an organohalide and an organoboron compound,[1] is
an attractive cross-coupling reaction for use in the synthesis of natural products [2] and …