Synthesis of α-Branched Amines by Three- And Four-Component C–H Functionalization Employing a Readily Diversifiable Hydrazone Directing Group

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Abstract

Efficient syntheses of α-branched amines by three- and four-component C–H functionalization employing a diversifiable hydrazone directing group have been developed. The hydrazone in the α-branched amine products has been readily converted to multiple desirable functionalities such as a nitrile, a carboxylic acid, alkenes, and heterocycles using diverse heterolytic chemistry and homolytic transition metal- or photoredox-catalyzed processes. This study represents the first example of a four-component C–H functionalization reaction.

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Brandes, D. S., Muma, A. D., & Ellman, J. A. (2021). Synthesis of α-Branched Amines by Three- And Four-Component C–H Functionalization Employing a Readily Diversifiable Hydrazone Directing Group. Organic Letters, 23(24), 9597–9601. https://doi.org/10.1021/acs.orglett.1c03807

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