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.
Authors
- Hongquan Yin
- Xinzhe Zhao
- Fu‐Xue Chen (ORCID: https://orcid.org/0000-0002-9091-2147)
Institutions
- Beijing Institute of Technology (CN)
- Shanghai Liangyou (China) (CN)
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
- Field-Weighted Citation Impact
- 0.00