CpxM(iii)-catalyzed enantioselective C-H functionalization through migratory insertion of metal-carbenes/nitrenes. Academic Article uri icon

Overview

abstract

  • CpxM(iii)-catalyzed enantioselective C-H functionalization reactions have progressed rapidly using either chiral cyclopentadienyl ligands or appropriate chiral carboxylic acids. In this context, highly reactive carbene and nitrene precursors can serve as effective C-H coupling partners, providing a straightforward and efficient approach to access chiral molecules. In this review, we highlight the developments in CpxM(iii)-catalyzed enantioselective C-H functionalization reactions through migratory insertion of metal-carbenes/nitrenes by employing chiral CpxM(iii) complexes or achiral CpxM(iii) complexes combined with chiral carboxylic acids.

publication date

  • August 17, 2021

Identity

Scopus Document Identifier

  • 85114254514

Digital Object Identifier (DOI)

  • 10.1039/d1ob01248g

PubMed ID

  • 34612356

Additional Document Info

volume

  • 19

issue

  • 34