Ce(OTf)<sub>3</sub>-Catalyzed Asymmetric 6π Cyclization of Triaryldivinyl Ketones

The rare-earth Ce(OTf)<sub>3</sub>-catalyzed asymmetric 6π cyclization of triaryldivinyl ketones is realized, affording methyl (<i>R</i>,<i>E</i>)-1-aryl-2-arylmethylidene-3-hydroxy-1,4-dihydronaphthalene-2-carboxylates in moderate to good yields with good to excellent enantioselectivities. The reaction provides a new strategy for the construction of optically active 3-hydroxy-1,4-dihydronaphthalene-2-carboxylic acid derivatives.

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Publication Details

Journal
Organic Letters
Published
2025-05-01
DOI
https://doi.org/10.1021/acs.orglett.5c01081
Citations
6
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
5.62

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article

Ce(OTf)3-Catalyzed Asymmetric 6π Cyclization of Triaryldivinyl Ketones

Wei Hao, Zhanhui Yang, Liu Li, Jiaxi Xu
6 citations
Organic Letters
Catalytic Alkyne Reactions
5.62
article

Ce(OTf)3-Catalyzed Asymmetric 6π Cyclization of Triaryldivinyl Ketones

Wei Hao, Zhanhui Yang, Liu Li, Jiaxi Xu
article en
6 citations

Abstract

The rare-earth Ce(OTf)<sub>3</sub>-catalyzed asymmetric 6π cyclization of triaryldivinyl ketones is realized, affording methyl (<i>R</i>,<i>E</i>)-1-aryl-2-arylmethylidene-3-hydroxy-1,4-dihydronaphthalene-2-carboxylates in moderate to good yields with good to excellent enantioselectivities. The reaction provides a new strategy for the construction of optically active 3-hydroxy-1,4-dihydronaphthalene-2-carboxylic acid derivatives.

Organic LettersVol. 27(19)
Beijing University of Chemical Technology (CN)
National Key Research and Development Program of China
Openalex Percentile: Top 4%
Catalytic Alkyne Reactions
5.62
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