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Oxidative 1,2-carboamination of alkenes with alkyl nitriles and amines toward ?-amino alkyl nitriles.

ABSTRACT: Difunctionalization of alkenes has become a powerful tool for quickly increasing molecular complexity in synthesis. Despite significant progress in the area of alkene difunctionalization involving the incorporation of a nitrogen atom across the C-C double bonds, approaches for the direct 1,2-carboamination of alkenes to produce linear N-containing molecules are scarce and remain a formidable challenge. Here we describe a radical-mediated oxidative intermolecular 1,2-alkylamination of alkenes with alkyl nitriles and amines involving C(sp³)-H oxidative functionalization catalysed by a combination of Ag₂CO₃ with iron Lewis acids. This three-component alkene 1,2-alkylamination method is initiated by the C(sp³)-H oxidative radical functionalization, which enables one-step formation of two new chemical bonds, a C-C bond and a C-N bond, to selectively produce ?-amino alkyl nitriles.

SUBMITTER: Liu YY

PROVIDER: S-EPMC5394231 | biostudies-literature | 2017 Apr

REPOSITORIES: biostudies-literature

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Oxidative 1,2-carboamination of alkenes with alkyl nitriles and amines toward γ-amino alkyl nitriles.

Liu Yan-Yun YY Yang Xu-Heng XH Song Ren-Jie RJ Luo Shenglian S Li Jin-Heng JH

Nature communications 20170410

Difunctionalization of alkenes has become a powerful tool for quickly increasing molecular complexity in synthesis. Despite significant progress in the area of alkene difunctionalization involving the incorporation of a nitrogen atom across the C-C double bonds, approaches for the direct 1,2-carboamination of alkenes to produce linear N-containing molecules are scarce and remain a formidable challenge. Here we describe a radical-mediated oxidative intermolecular 1,2-alkylamination of alkenes wit ...[more]

PMID: 28393864

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