Lewis Acid-catalyzed Formal 1,3-Hydroxy Migration of Arylvinyl Carbinols

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.

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Publication Details

Journal
Synlett
Published
2025-11-06
DOI
https://doi.org/10.1055/a-2740-4940
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.00
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article

Lewis Acid-catalyzed Formal 1,3-Hydroxy Migration of Arylvinyl Carbinols

Keiji Mori, Tomoko Kawasaki‐Takasuka, Koutarou Amano
Synlett
Catalytic C–H Functionalization Methods
article

Lewis Acid-catalyzed Formal 1,3-Hydroxy Migration of Arylvinyl Carbinols

Keiji Mori, Tomoko Kawasaki‐Takasuka, Koutarou Amano
article en

Abstract

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.

SynlettVol. 37(04)
Tokyo University of Agriculture and Technology (JP)
Openalex Percentile: Top 75%
Catalytic C–H Functionalization Methods
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