Research shows regioselective hydroalkynylation improves chiral nitrile synthesis, implying potential for selective synthesis.
Unactivated alkenes represent a challenging substrate for selective functionalization, particularly in achieving both regioselectivity and enantioselectivity. In this study, we present a strategy for the regio- and enantioselective hydroalkynylation of unactivated alkenes through the integration of noncovalent π⋯π interactions between the cyano group of the substrate and a chiral bis(oxazoline) ligand. The weak π⋯π interaction was supported by control experiments and computational studies. The method provides a reliable approach for synthesizing chiral nitriles with remote (β-, γ-, and δ-) stereocenters, which exhibit orthogonal reactivities and serve as valuable intermediates for further derivatization into otherwise difficult-to-access compounds. Our work provides a strategy for olefin functionalization and opens up avenues for the selective synthesis of chiral nitriles with remote stereocenters.
No takes yet. Share an insight, caveat, or question.
Chao Wang (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: