Cu(I)-Catalyzed Highly Regioselective C–H Amidation\nof Quinoline <i>N</i>‑Oxides with Dioxazolones

A Cu(I)-catalyzed\nhighly regioselective synthesis of 2-acetamidequinoline <i>N</i>-oxides using dioxazolones with quinoline <i>N</i>-oxides\nhas been reported. The reaction possesses mild reaction conditions\nand excellent functional group compatibility. Furthermore, the addition\nof hydrochloric acid promotes the decomposition of copper complexes,\nwhich is beneficial for postprocessing.

Publication Details

Journal
Figshare
Published
2024-09-30
DOI
https://doi.org/10.1021/acs.orglett.4c03118.s002
Primary Topic
Diverse Scientific and Economic Studies
Type
article
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article

Cu(I)-Catalyzed Highly Regioselective C–H Amidation\nof Quinoline N‑Oxides with Dioxazolones

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Diverse Scientific and Economic Studies
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Cu(I)-Catalyzed Highly Regioselective C–H Amidation\nof Quinoline N‑Oxides with Dioxazolones

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Abstract

A Cu(I)-catalyzed\nhighly regioselective synthesis of 2-acetamidequinoline <i>N</i>-oxides using dioxazolones with quinoline <i>N</i>-oxides\nhas been reported. The reaction possesses mild reaction conditions\nand excellent functional group compatibility. Furthermore, the addition\nof hydrochloric acid promotes the decomposition of copper complexes,\nwhich is beneficial for postprocessing.

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Openalex Percentile: Top 49%
Diverse Scientific and Economic Studies
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Cu(I)-Catalyzed Highly Regioselective C–H Amidation\nof Quinoline <i>N</i>‑Oxides with Dioxazolones · Figshare (2024) | TGRS Research Map | TGRS