Direct <i>N</i>-methyl C–H esterification of <i>O</i>-tosyl hydroxamates to enable facile synthesis of hemiaminal esters

Here we present a new method for synthesizing amide hemiaminal esters through the direct <i>N</i>-methyl C-H esterification of <i>O</i>-tosyl hydroxamates. This approach demonstrates good tolerance for a variety of functional groups and operates under mild, transition-metal-free conditions, thus providing an accessible and effective pathway to hemiaminal esters.

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Journal
Chemical Communications
Published
2025-01-01
DOI
https://doi.org/10.1039/d5cc02570b
Citations
1
Primary Topic
Synthesis and Catalytic Reactions
Type
article
Field-Weighted Citation Impact
0.94
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article

Direct N-methyl C–H esterification of O-tosyl hydroxamates to enable facile synthesis of hemiaminal esters

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1 citations
Chemical Communications
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article

Direct N-methyl C–H esterification of O-tosyl hydroxamates to enable facile synthesis of hemiaminal esters

Jianjun Dai, Hua Xiao, Zhiwen Luo, Yan Pan, Heng Yang, Jicheng Wu, Fei Cao
article en
1 citations

Abstract

Here we present a new method for synthesizing amide hemiaminal esters through the direct <i>N</i>-methyl C-H esterification of <i>O</i>-tosyl hydroxamates. This approach demonstrates good tolerance for a variety of functional groups and operates under mild, transition-metal-free conditions, thus providing an accessible and effective pathway to hemiaminal esters.

Chemical CommunicationsVol. 61(57)
Hefei University of Technology (CN)
Openalex Percentile: Top 25%
Synthesis and Catalytic Reactions
0.94
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