Silver‐Catalyzed Oxidative Ring‐Opening of Cyclic Aliphatic Amines for C−H Alkylation of Cyclic Aldimines

Abstract The developed methodology describes the synthesis of distal aminoalkyl‐substituted cyclic aldimines through a silver‐catalyzed site‐selective ring‐opening of N ‐acylated cyclic amines and decarboxylative C−H alkylation of cyclic aldimines. This method enjoys water as a sustainable solvent, which offers advantages including high stereoselectivity, good functional group compatibility, and a broad substrate scope. Preliminary studies indicate that a radical process might be involved in the reaction.

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Publication Details

Journal
Advanced Synthesis & Catalysis
Published
2025-03-17
DOI
https://doi.org/10.1002/adsc.202500002
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.94
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article

Silver‐Catalyzed Oxidative Ring‐Opening of Cyclic Aliphatic Amines for C−H Alkylation of Cyclic Aldimines

Haiqing Luo, Guisheng Chen, Xiaolan Li, Jie Liu
1 citations
Advanced Synthesis & Catalysis
Catalytic C–H Functionalization Methods
0.94
article

Silver‐Catalyzed Oxidative Ring‐Opening of Cyclic Aliphatic Amines for C−H Alkylation of Cyclic Aldimines

Haiqing Luo, Guisheng Chen, Xiaolan Li, Jie Liu
article en
1 citations

Abstract

Abstract The developed methodology describes the synthesis of distal aminoalkyl‐substituted cyclic aldimines through a silver‐catalyzed site‐selective ring‐opening of N ‐acylated cyclic amines and decarboxylative C−H alkylation of cyclic aldimines. This method enjoys water as a sustainable solvent, which offers advantages including high stereoselectivity, good functional group compatibility, and a broad substrate scope. Preliminary studies indicate that a radical process might be involved in the reaction.

Advanced Synthesis & CatalysisVol. 367(11)
Nanchang University (CN), Gannan Normal University (CN)
Openalex Percentile: Top 28%
Catalytic C–H Functionalization Methods
0.94
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