Palladium-Catalyzed Domino Heck/Intermolecular Cross Coupling Reaction for the Synthesis of 3-Alkyl Substituted Indene Derivatives

Indene derivatives are one of the core skeletons of many natural products and drugs, and are widely used in medicine, materials and other fields.It is of great significance to develop a simple and efficient method for the synthesis of indene derivatives.In this work, iodobenzenes with proximity linking unactivated olefins undergo palladium-catalyzed intramolecular Heck reaction to generate alkylpalladium(II) intermediates, which induce the intramolecular nucleophilic cyclization of 2-(2-phenylethynyl)phenylmalonate diethyl ester to afford a series of 3-alkyl substituted indene derivatives.The reaction has the advantages of mild conditions, simple operation, high yield and wide applicability of substrates, which provides a new strategy for the synthesis of indene derivatives.

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Publication Details

Journal
Chinese Journal of Organic Chemistry
Published
2025-01-01
DOI
https://doi.org/10.6023/cjoc202407029
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Palladium-Catalyzed Domino Heck/Intermolecular Cross Coupling Reaction for the Synthesis of 3-Alkyl Substituted Indene Derivatives

Tuanli Yao, Tao Li, Linlin Wang
Chinese Journal of Organic Chemistry
Catalytic Alkyne Reactions
article

Palladium-Catalyzed Domino Heck/Intermolecular Cross Coupling Reaction for the Synthesis of 3-Alkyl Substituted Indene Derivatives

Tuanli Yao, Tao Li, Linlin Wang
article en

Abstract

Indene derivatives are one of the core skeletons of many natural products and drugs, and are widely used in medicine, materials and other fields.It is of great significance to develop a simple and efficient method for the synthesis of indene derivatives.In this work, iodobenzenes with proximity linking unactivated olefins undergo palladium-catalyzed intramolecular Heck reaction to generate alkylpalladium(II) intermediates, which induce the intramolecular nucleophilic cyclization of 2-(2-phenylethynyl)phenylmalonate diethyl ester to afford a series of 3-alkyl substituted indene derivatives.The reaction has the advantages of mild conditions, simple operation, high yield and wide applicability of substrates, which provides a new strategy for the synthesis of indene derivatives.

Chinese Journal of Organic ChemistryVol. 45(4)
Xi'an University of Science and Technology (CN), Shaanxi University of Science and Technology (CN)
National Key Research and Development Program of China
Openalex Percentile: Top 92%
Catalytic Alkyne Reactions
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