Palladium‐Catalyzed Intramolecular Asymmetric Allylic Amidation: A General Route to 5‐Substituted Chiral Oxazolines

, promotes the cyclization with high efficiency and enantiocontrol. The reaction demonstrates broad substrate scope and excellent functional group tolerance, accommodating a wide range of sterically diverse 2-substituents and electronically varied aryl allylic units, delivering the desired 5-vinyl oxazolines in good yields with high enantioselectivity (up to 99% ee).

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Publication Details

Journal
Chemistry - A European Journal
Published
2026-04-25
DOI
https://doi.org/10.1002/chem.71046
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Palladium‐Catalyzed Intramolecular Asymmetric Allylic Amidation: A General Route to 5‐Substituted Chiral Oxazolines

Xu Bao, Yong Su
Chemistry - A European Journal
Catalytic C–H Functionalization Methods
article

Palladium‐Catalyzed Intramolecular Asymmetric Allylic Amidation: A General Route to 5‐Substituted Chiral Oxazolines

Xu Bao, Yong Su
article en

Abstract

, promotes the cyclization with high efficiency and enantiocontrol. The reaction demonstrates broad substrate scope and excellent functional group tolerance, accommodating a wide range of sterically diverse 2-substituents and electronically varied aryl allylic units, delivering the desired 5-vinyl oxazolines in good yields with high enantioselectivity (up to 99% ee).

Chemistry - A European Journal
Lanzhou University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 8%
Catalytic C–H Functionalization Methods
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