Diverse Reaction Pathways Tuned by Nucleophilicity: Studies on Reactions of <i>N</i> -Methoxymethyl- <i>N</i> -(trimethylsilyl)methylbenzylamine and Different Double Bonds

-(trimethylsilyl)methylbenzylamine and unsaturated compounds and guidance on the structural prediction of products generated from unsymmetric azomethine ylide precursors.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-04-30
DOI
https://doi.org/10.1021/acs.joc.5c03256
Primary Topic
Organic Chemistry Cycloaddition Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Diverse Reaction Pathways Tuned by Nucleophilicity: Studies on Reactions of N -Methoxymethyl- N -(trimethylsilyl)methylbenzylamine and Different Double Bonds

Yuliang Wei, Jiaxi Xu
The Journal of Organic Chemistry
Organic Chemistry Cycloaddition Reactions
article

Diverse Reaction Pathways Tuned by Nucleophilicity: Studies on Reactions of N -Methoxymethyl- N -(trimethylsilyl)methylbenzylamine and Different Double Bonds

Yuliang Wei, Jiaxi Xu
article en

Abstract

-(trimethylsilyl)methylbenzylamine and unsaturated compounds and guidance on the structural prediction of products generated from unsymmetric azomethine ylide precursors.

The Journal of Organic Chemistry
Beijing University of Chemical Technology (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 14%
Organic Chemistry Cycloaddition Reactions
DOISourceOpenAlex
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Diverse Reaction Pathways Tuned by Nucleophilicity: Studies on Reactions of <i>N</i> -Methoxymethyl- <i>N</i> -(trimethylsilyl)methylbenzylamine and Different Double Bonds — Yuliang Wei, Jiaxi Xu · The Journal of Organic Chemistry (2026) | TGRS Research Map | TGRS