Deprotection and Functionalization of Protective N‐Heterocycles Under Mild Conditions

A mild and versatile potassium trimethylsilanolate/butyronitrile (KOTMS/PrCN) reaction system for the deprotection and further functionalization of N‐heterocycles in a single step is developed. A range of N‐heterocycles, attached by various protecting groups, can be well transformed with good yields and functionality tolerance. The protocol features high efficiency, simple operation, and synthetic application.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-04-03
DOI
https://doi.org/10.1002/ejoc.202500165
Citations
1
Primary Topic
Synthesis of Indole Derivatives
Type
article
Field-Weighted Citation Impact
0.94
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article

Deprotection and Functionalization of Protective N‐Heterocycles Under Mild Conditions

Feng Zhao, Qianyu Zhang, Zixuan Tan, Wenjing Liu
1 citations
European Journal of Organic Chemistry
Synthesis of Indole Derivatives
0.94
article

Deprotection and Functionalization of Protective N‐Heterocycles Under Mild Conditions

Feng Zhao, Qianyu Zhang, Zixuan Tan, Wenjing Liu
article en
1 citations

Abstract

A mild and versatile potassium trimethylsilanolate/butyronitrile (KOTMS/PrCN) reaction system for the deprotection and further functionalization of N‐heterocycles in a single step is developed. A range of N‐heterocycles, attached by various protecting groups, can be well transformed with good yields and functionality tolerance. The protocol features high efficiency, simple operation, and synthetic application.

European Journal of Organic ChemistryVol. 28(21)
Hunan University of Traditional Chinese Medicine (CN), Hunan University (CN)
Openalex Percentile: Top 27%
Synthesis of Indole Derivatives
0.94
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