Ontology highlight
ABSTRACT:
SUBMITTER: Gillis EP
PROVIDER: S-EPMC7249414 | biostudies-literature | 2008 Oct
REPOSITORIES: biostudies-literature
Journal of the American Chemical Society 20081007 43
Due to its sensitivity to most synthetic reagents, it is typically necessary to introduce the boronic acid functional group just prior to its utilization. Overcoming this important limitation, we herein report that air- and chromatographically stable MIDA boronates are compatible with a wide range of common reagents which enables the multistep synthesis of complex boronic acid building blocks from simple B-containing starting materials. X-ray and variable temperature NMR studies link the unique ...[more]