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Recent Advances and Strategies for the Transition-Metal-Catalyzed C−H Functionalization of N-Nitrosoanilines

dc.contributor.authorChaudhary P.; Kandasamy J.; Macabeo A.P.G.; Tamargo R.J.I.; Lee Y.R.
dc.date.accessioned2025-05-23T11:26:32Z
dc.description.abstractThe challenges faced in the activation and functionalization of C−H bonds while producing high-value aromatic intermediates are significant for synthetic organic chemistry. This review summarizes the advancements made toward the C−H functionalization of N-nitrosoanilines in the past decade, in which the nitroso group coordinates to a transition metal, such as rhodium, palladium, cobalt, iridium, and ruthenium, acting as a directing group to allow the activation of the ortho C−H bond. The versatility of this synthetic approach has led to the regio- and chemoselective introduction of various functional groups giving rise to aromatic congeners with diverse functional and structural properties. C−H functionalized nitroso compounds can be further transformed into valuable synthetic intermediates and unique heterocyclic compounds. A description of the mechanism underlying each reaction is also included. This review includes the following sections:. (Figure presented.). © 2021 Wiley-VCH GmbH
dc.identifier.doihttps://doi.org/10.1002/adsc.202001613
dc.identifier.urihttp://172.23.0.11:4000/handle/123456789/10413
dc.relation.ispartofseriesAdvanced Synthesis and Catalysis
dc.titleRecent Advances and Strategies for the Transition-Metal-Catalyzed C−H Functionalization of N-Nitrosoanilines

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