Alkenyl Fluorosulfates—Expedient Partners for Palladium‐Catalyzed Cross‐Coupling Reactions
were documented. Reactivity of alkenyl fluorosulfates in Suzuki, Sonogashira, Heck, Stille, and Buchwald-Hartwig reactions, as well as Miyaura borylation under typical conditions, was studied, and limitations of the methods were established. It was found that alkenyl flurosulfates have similar or even higher reactivity in the cross-coupling reactions as compared to alkenyl triflates.
Authors
- Serhii Zhersh
- Vladyslav Hnativ
- Oleksandr O. Grygorenko (ORCID: https://orcid.org/0000-0002-6036-5859)
- Serhii Aleksandrenko
Institutions
- Taras Shevchenko National University of Kyiv (UA)
- Enamine (Ukraine) (UA)
Publication Details
- Journal
- Chemistry - A European Journal
- Published
- 2026-05-09
- DOI
- https://doi.org/10.1002/chem.71098
- Primary Topic
- Catalytic Cross-Coupling Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Ministry of Education and Science of Ukraine