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DOI: 10.1055/a-2740-4940
Lewis Acid-catalyzed Formal 1,3-Hydroxy Migration of Arylvinyl Carbinols
Autoren
This work was partially supported by a Grant-in-Aid for Scientific Research from the Japan Society for the Promotion of Science.

Abstract
Although the 1,3-hydroxy migration reaction of arylvinyl carbinols is a valuable molecular transformation, examples of Lewis acid-catalyzed reactions remain quite limited. We found that the target Lewis acid-catalyzed reaction proceeded smoothly when acetone was used as the reaction medium. This catalytic system was applicable to arylvinyl carbinols having electron-deficient aromatic rings, a little-studied and challenging topic in 1,3-hydroxy migration chemistry.
Keywords
1,3-Hydroxy migration - Lewis acids - Cinnamyl alcohols - Arylvinyl carbinols - Catalytic reactionPublikationsverlauf
Eingereicht: 26. August 2025
Angenommen nach Revision: 06. November 2025
Accepted Manuscript online:
06. November 2025
Artikel online veröffentlicht:
26. November 2025
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For selected reviews on 1,3-hydroxy migration of allylic alcohols, see:
For selected examples of 1,3-hydroxy migration of allylic alcohols, see:
See, also:
For selected recent examples of Lewis-acid catalyzed reaction developed by our group, see:
Lewis acid-catalyzed 1,3-migration of aminomethyl group developed by our group, see:
Momiyama group also developed same kind of reaction catalyzed by Brønsted acid, see: