Methods for the Vinylation of Alcohols (A Review)
Vinyl ethers bearing the fragment RO–CH=CH2, where R is an alkyl or aryl substituent, are valuable substrates for organic synthesis and polymer chemistry. The double carbon–carbon bond is highly reactive and can be used in a wide variety of organic transformations, including addition processes—particularly cycloaddition and polymerization reactions. Recent investigations in this field have demonstrated the significant potential of subsequent transformations: vinylation of alcohols, cycloaddition of vinyl ethers, and alcohol release. Combination of these processes enables the introduction of a C2 fragment into a wide range of organic molecules. Due to these advancements, vinylation of alcohols has become a cornerstone in organic synthesis. This review focuses on an overview of important approaches to the vinylation of alcohols and highlights recent achievements in this field.
Authors
- Vladimir V. Voronin (ORCID: https://orcid.org/0000-0002-5589-4705)
- Maria S. Ledovskaya (ORCID: https://orcid.org/0000-0002-5198-2927)
- Anna A. Reznichenko
Institutions
- St Petersburg University (RU)
Publication Details
- Journal
- Russian Journal of General Chemistry
- Published
- 2025-12-01
- DOI
- https://doi.org/10.1134/s1070363225606313
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.00