Dehydroxyselenocyanation of alcohols under grinding conditions

A novel strategy for dehydroxyselenocyanation of alcohols, utilizing a readily available electrophilic selenocyanating reagent <i>N</i>-selenocyanatophthalimide in combination with triphenylphosphine under grinding conditions within 2 min at room temperature was developed. This solvent-free methodology is time-efficient and features a broad substrate scope, enabling the late-stage functionalization of diverse pharmaceutical molecules and natural products.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ob00305a
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
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article

Dehydroxyselenocyanation of alcohols under grinding conditions

Hongquan Yin, Xinzhe Zhao, Fu‐Xue Chen
Organic & Biomolecular Chemistry
Sulfur-Based Synthesis Techniques
article

Dehydroxyselenocyanation of alcohols under grinding conditions

Hongquan Yin, Xinzhe Zhao, Fu‐Xue Chen
article en

Abstract

A novel strategy for dehydroxyselenocyanation of alcohols, utilizing a readily available electrophilic selenocyanating reagent <i>N</i>-selenocyanatophthalimide in combination with triphenylphosphine under grinding conditions within 2 min at room temperature was developed. This solvent-free methodology is time-efficient and features a broad substrate scope, enabling the late-stage functionalization of diverse pharmaceutical molecules and natural products.

Organic & Biomolecular ChemistryVol. 23(19)
Beijing Institute of Technology (CN), Shanghai Liangyou (China) (CN)
Openalex Percentile: Top 94%
Sulfur-Based Synthesis Techniques
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