Development of Configurationally Labile Biaryl Reagents for Atropisomer Synthesis
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DOI: 10.1002/ejoc.202400402
Abstract: Axially chiral biaryl scaffolds are important in pharmaceuticals, natural products, and asymmetric synthesis. Atroposelective ring‐opening of configurationally labile biaryl reagents via dynamic kinetic asymmetric transformation provides a valuable approach to access axially chiral biaryl atropisomers.… read more here.
Keywords: development configurationally; configurationally labile; labile biaryl; biaryl reagents ... See more keywords