Copper-Catalyzed Diamination of Alkenes using <i>o</i>‑Benzoylhydroxylamines to Access the Four Azaindoline\nFamilies

A mild\nand efficient method for the copper-catalyzed diamination\nof alkenes is described. In this reaction, <i>o</i>-benzoylhydroxylamine\nserves as an electrophilic nitrogen source for the regioselective\nformation of C–N bonds. This transformation provides a novel\nstrategy for synthesizing all four isomeric 2,3-disubstituted azaindoline\nfamilies and offers a wide substrate scope.

Publication Details

Journal
Figshare
Published
2024-10-04
DOI
https://doi.org/10.1021/acs.orglett.4c02585.s001
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

Copper-Catalyzed Diamination of Alkenes using o‑Benzoylhydroxylamines to Access the Four Azaindoline\nFamilies

Figshare
Catalytic C–H Functionalization Methods
article

Copper-Catalyzed Diamination of Alkenes using o‑Benzoylhydroxylamines to Access the Four Azaindoline\nFamilies

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Abstract

A mild\nand efficient method for the copper-catalyzed diamination\nof alkenes is described. In this reaction, <i>o</i>-benzoylhydroxylamine\nserves as an electrophilic nitrogen source for the regioselective\nformation of C–N bonds. This transformation provides a novel\nstrategy for synthesizing all four isomeric 2,3-disubstituted azaindoline\nfamilies and offers a wide substrate scope.

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Catalytic C–H Functionalization Methods
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Copper-Catalyzed Diamination of Alkenes using <i>o</i>‑Benzoylhydroxylamines to Access the Four Azaindoline\nFamilies · Figshare (2024) | TGRS Research Map | TGRS