Rhodium‐Catalyzed Regioselective Addition of <i>N</i> ‐Hydroxyl Imides to Internal Alkynes

An intermolecular rhodium‐catalyzed regioselective addition of N ‐hydroxyl imides to internal alkynes leads to branched O ‐allyl compounds, which can be readily transformed to allylic alcohols and O ‐allyl hydroxylamines after deprotection. Isotopic labeling experiments suggest a plausible reaction mechanism.

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Publication Details

Journal
Israel Journal of Chemistry
Published
2026-04-02
DOI
https://doi.org/10.1002/ijch.70014
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Rhodium‐Catalyzed Regioselective Addition of N ‐Hydroxyl Imides to Internal Alkynes

Zi Liu, Bernhard Breit
Israel Journal of Chemistry
Catalytic C–H Functionalization Methods
article

Rhodium‐Catalyzed Regioselective Addition of N ‐Hydroxyl Imides to Internal Alkynes

Zi Liu, Bernhard Breit
article en

Abstract

An intermolecular rhodium‐catalyzed regioselective addition of N ‐hydroxyl imides to internal alkynes leads to branched O ‐allyl compounds, which can be readily transformed to allylic alcohols and O ‐allyl hydroxylamines after deprotection. Isotopic labeling experiments suggest a plausible reaction mechanism.

Israel Journal of ChemistryVol. 66(3)
University of Freiburg (DE)
Deutsche Forschungsgemeinschaft
Openalex Percentile: Top 25%
Catalytic C–H Functionalization Methods
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