Sc(OTf)3/Cu(CH3CN)4PF6-Catalyzed Highly Chemo- and Regio-Selectivity Prenylation of Phenols with 1,1-Dimethylallylalkohols

Herein, we reported Sc(OTf)3/Cu(CH3CN)4PF6-catalyzed prenylation of phenols with highly chemo- and region-selectivity under mild condition via easy available catalysts, affording the corresponding prenylated products in good to excellent yield. Through this catalytic system alkylation of phenols with various allylic alcohols was also achieved in excellent selectivity and yield. Furthermore, this methodology was used to modification of nature products containing phenols, which might be used for investigating the structure-activity relationship.

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Publication Details

Journal
Synlett
Published
2026-06-18
DOI
https://doi.org/10.1055/a-2899-0609
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.00
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article

Sc(OTf)3/Cu(CH3CN)4PF6-Catalyzed Highly Chemo- and Regio-Selectivity Prenylation of Phenols with 1,1-Dimethylallylalkohols

Y Zhang, Xudong Gao, Yueqi Zhu, Xiaolei Wang et al.
Synlett
Catalytic Alkyne Reactions
article

Sc(OTf)3/Cu(CH3CN)4PF6-Catalyzed Highly Chemo- and Regio-Selectivity Prenylation of Phenols with 1,1-Dimethylallylalkohols

Y Zhang, Xudong Gao, Yueqi Zhu, Xiaolei Wang, Panpan Wang, Xue Zhang
article en

Abstract

Herein, we reported Sc(OTf)3/Cu(CH3CN)4PF6-catalyzed prenylation of phenols with highly chemo- and region-selectivity under mild condition via easy available catalysts, affording the corresponding prenylated products in good to excellent yield. Through this catalytic system alkylation of phenols with various allylic alcohols was also achieved in excellent selectivity and yield. Furthermore, this methodology was used to modification of nature products containing phenols, which might be used for investigating the structure-activity relationship.

Synlett
Lanzhou Petrochemical Polytechnic (CN), Lanzhou University (CN)
Openalex Percentile: Top 11%
Catalytic Alkyne Reactions
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