Litcius/Paper detail

Single‐Step Synthesis of Atropisomers with Vicinal C−C and C−N Diaxes by Cobalt‐Catalyzed Atroposelective C−H Annulation

Bingjie Wang, Guo‐Xiong Xu, Zong‐Wei Huang, Xu Wu, Xin Hong, Qi‐Jun Yao, Bing‐Feng Shi

2022Angewandte Chemie International Edition114 citationsDOIOpen Access PDF

Abstract

The atroposelective synthesis of atropisomers with vicinal diaxes remains rare and challenging, due to the steric influence between the two axes and their unique topology. Herein, we disclose a single-step construction of atropisomers with vicinal C-C and C-N chiral diaxes by cyclopentadiene (Cp)-free cobalt-catalyzed intramolecular atroposelective C-H annulation, providing the desired diaxial atropisomers of unique structures with decent stereocontrols of both axes (up to >99 % ee and 70 : 1 dr). The optically pure products bearing fluorophores show circular polarized luminescence (CPL) properties, being candidate materials for potential CPL applications. Atropisomerization experiments and density function theory (DFT) calculations are conducted to study the rotational barriers and rotation pathways of the diaxes.

Topics & Concepts

VicinalAtropisomerAnnulationCobaltCatalysisChemistryStereochemistryCombinatorial chemistryOrganic chemistryAxial and Atropisomeric Chirality SynthesisCatalytic C–H Functionalization MethodsMetal-Organic Frameworks: Synthesis and Applications