Ruthenium(II)-Catalyzed\nRemote C–H Alkylation\nof Arenes Using Diverse N‑Directing Groups through Aziridine\nRing Opening

An efficient approach for the remote C–H alkylation\nof arenes,\nemploying a variety of N-directing groups is described. This method\nfacilitates the straightforward synthesis of valuable phenylethylamine\nderivatives by exclusively cleaving the benzylic C–N bond in\naziridines. Furthermore, these products can easily remove the protecting\ngroups, resulting in a variety of meta-substituted compounds, such\nas amines and ketones, which hold significance in synthetic chemistry.

Publication Details

Journal
Figshare
Published
2024-09-12
DOI
https://doi.org/10.1021/acs.orglett.4c02254.s001
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
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article

Ruthenium(II)-Catalyzed\nRemote C–H Alkylation\nof Arenes Using Diverse N‑Directing Groups through Aziridine\nRing Opening

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Catalytic C–H Functionalization Methods
article

Ruthenium(II)-Catalyzed\nRemote C–H Alkylation\nof Arenes Using Diverse N‑Directing Groups through Aziridine\nRing Opening

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Abstract

An efficient approach for the remote C–H alkylation\nof arenes,\nemploying a variety of N-directing groups is described. This method\nfacilitates the straightforward synthesis of valuable phenylethylamine\nderivatives by exclusively cleaving the benzylic C–N bond in\naziridines. Furthermore, these products can easily remove the protecting\ngroups, resulting in a variety of meta-substituted compounds, such\nas amines and ketones, which hold significance in synthetic chemistry.

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Openalex Percentile: Top 72%
Catalytic C–H Functionalization Methods
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Ruthenium(II)-Catalyzed\nRemote C–H Alkylation\nof Arenes Using Diverse N‑Directing Groups through Aziridine\nRing Opening · Figshare (2024) | TGRS Research Map | TGRS