Beilstein J. Org. Chem.2026,22, 882–887, doi:10.3762/bjoc.22.68
facial selectivity during electrophilic trapping. These findings expand the synthetic utility of α-boryl lithium intermediates and provide insight into the origins of their diastereoselectivity.
Keywords: α-boryl lithium; diastereoselectivity; (iodomethyl)cyclopropylboronicesters; ring-opening
PDF
Graphical Abstract
Scheme 1:
Synthesis and reactivity of α-boryl lithium species.