Asymmetric synthesis of isoindolines <i>via</i> a palladium-catalyzed enantioselective intramolecular oxidative aminoacetoxylation reaction

Here, we report a palladium-catalyzed asymmetric intramolecular oxidative aminoacetoxylation reaction employing triazole-oxazoline ligands, which enables the direct construction of a chiral isoindoline scaffold. A series of chiral isoindolines bearing vicinal stereocenters were obtained in moderate to high yields and good enantiomeric ratios under mild conditions.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-12-04
DOI
https://doi.org/10.1039/d5ob01595b
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

Asymmetric synthesis of isoindolines via a palladium-catalyzed enantioselective intramolecular oxidative aminoacetoxylation reaction

Kewei Hu, Binggang Wang, Jongseok Kang, Zhiguang Song et al.
Organic & Biomolecular Chemistry
Catalytic C–H Functionalization Methods
article

Asymmetric synthesis of isoindolines via a palladium-catalyzed enantioselective intramolecular oxidative aminoacetoxylation reaction

Kewei Hu, Binggang Wang, Jongseok Kang, Zhiguang Song, Dongyuan Ju
article en

Abstract

Here, we report a palladium-catalyzed asymmetric intramolecular oxidative aminoacetoxylation reaction employing triazole-oxazoline ligands, which enables the direct construction of a chiral isoindoline scaffold. A series of chiral isoindolines bearing vicinal stereocenters were obtained in moderate to high yields and good enantiomeric ratios under mild conditions.

Organic & Biomolecular ChemistryVol. 24(3)
Jilin University (CN)
Openalex Percentile: Top 71%
Catalytic C–H Functionalization Methods
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