Directed, Remote Dirhodium C(sp3)-H Functionalization, Desaturative Annulation, and Desaturation

Iminodirhodium reactive intermediates generated in situ from O-tosyloximes using Rh2(esp)2 in CH2Cl2 at rt were exploited for an agile trichotomy of challenging transformations: (1) remote C-H functionalizations using an exceptionally broad diversity of inorganic and organic nucleophiles including several unconventional examples, for example, ethers and acyl silanes; (2) desaturative annulation, a biomimetic 1,3-methylene C-C ring-closure with an overall loss of two hydrogens; and (3) directed desaturation for the acceptor-less, regioselective creation of gamma,5- or gamma,5,e,C-olefins. Compared with typical iminyl transition-metal-mediated and 1,5-hydrogen atom-transfer (1,5-HAT) processes, iminodirhodium intermediates are largely underexplored, especially with respect to C(sp3)-H centers and, yet, have the potential to be transformative by virtue of their substrate breadth, regiocontrol, and elusive reaction modality. A substrate scope includes benzylic, allylic, propargylic, tertiary, and alpha-alkyloxy centers.

Automated summary

In this study, Iminodirhodium reactive intermediates were generated from O-tosyloximes and utilized for three challenging transformations, including remote C-H functionalization, desaturative annulation, and directed desaturation. These reactions, which have been underexplored in previous studies, were successfully achieved under mild conditions.