Enantioselective Synthesis of Bicyclo[4.3.0]nonatrienones via Palladium-Catalyzed Desymmetric 1,5-Enyne Cycloisomerization

We herein disclose a palladium-catalyzed asymmetric desymmetric cycloisomerization of alkynyl-tethered cyclohexadienes, providing optically pure hydrindanes with one tertiary and one quaternary stereocenter. This reaction features a broad substrate scope, high atom economy, and good to excellent enantioselectivities. In addition, the diene and enone motifs embedded in the products offer synthetic handles for further structural diversification.

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Publication Details

Journal
Organic Letters
Published
2026-01-21
DOI
https://doi.org/10.1021/acs.orglett.5c05377
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
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article

Enantioselective Synthesis of Bicyclo[4.3.0]nonatrienones via Palladium-Catalyzed Desymmetric 1,5-Enyne Cycloisomerization

Aijun Lin, Jiajun Lu, Shu Sen Wu, Hongyue Dong et al.
Organic Letters
Catalytic Alkyne Reactions
article

Enantioselective Synthesis of Bicyclo[4.3.0]nonatrienones via Palladium-Catalyzed Desymmetric 1,5-Enyne Cycloisomerization

Aijun Lin, Jiajun Lu, Shu Sen Wu, Hongyue Dong, Peng Sun, Cheng Wang
article en

Abstract

We herein disclose a palladium-catalyzed asymmetric desymmetric cycloisomerization of alkynyl-tethered cyclohexadienes, providing optically pure hydrindanes with one tertiary and one quaternary stereocenter. This reaction features a broad substrate scope, high atom economy, and good to excellent enantioselectivities. In addition, the diene and enone motifs embedded in the products offer synthetic handles for further structural diversification.

Organic LettersVol. 28(5)
China Pharmaceutical University (CN), Xinjiang Institute of Materia Medica (CN), China Academy of Chinese Medical Sciences (CN), Institute of Chinese Materia Medica
Industry, innovation and infrastructure
Openalex Percentile: Top 82%
Catalytic Alkyne Reactions
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