Microwave-Assisted Palladium-Catalyzed Crossover-Annulation: Access to Fused Polycyclic Benzofuran Scaffolds

This study demonstrates quick access to heteroatom-embodied complex fused polycyclic frameworks through a palladium-catalyzed domino process facilitated by microwave-assisted crossover annulation of <i>o</i>-alkynylarylhalides and dihydrobenzofurans derivatives. The overall success of this process lies in the careful design of dihydrobenzofuran precursors that direct the initial palladium-mediated annulation step to proceed in a highly regioselective manner to furnish a single regioisomeric product. Notably, this one-pot method has witnessed good substrate scope and has furnished products with excellent yields.

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Publication Details

Journal
Organic Letters
Published
2024-12-25
DOI
https://doi.org/10.1021/acs.orglett.4c03917
Citations
4
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
1.00

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article

Microwave-Assisted Palladium-Catalyzed Crossover-Annulation: Access to Fused Polycyclic Benzofuran Scaffolds

Gedu Satyanarayana, Komal Goel
4 citations
Organic Letters
Catalytic Cross-Coupling Reactions
1.00
article

Microwave-Assisted Palladium-Catalyzed Crossover-Annulation: Access to Fused Polycyclic Benzofuran Scaffolds

Gedu Satyanarayana, Komal Goel
article en
4 citations

Abstract

This study demonstrates quick access to heteroatom-embodied complex fused polycyclic frameworks through a palladium-catalyzed domino process facilitated by microwave-assisted crossover annulation of <i>o</i>-alkynylarylhalides and dihydrobenzofurans derivatives. The overall success of this process lies in the careful design of dihydrobenzofuran precursors that direct the initial palladium-mediated annulation step to proceed in a highly regioselective manner to furnish a single regioisomeric product. Notably, this one-pot method has witnessed good substrate scope and has furnished products with excellent yields.

Organic LettersVol. 27(1)
Indian Institute of Technology Hyderabad (IN)
University Grants Commission, Science and Engineering Research Board
Openalex Percentile: Top 25%
Catalytic Cross-Coupling Reactions
1.00
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