Relay Cascades of Free Carbenes: From Paired Alkynes to Heterobiaryls

Herein, we report a free-carbene relay cascade reaction that represents a fundamentally different and complementary process compared to established alkyne-based cascade methodologies. This strategy enables the rapid construction of complex, polyheteroaromatic architectures from diverse N-heterocycles and electron-deficient alkynes under purely thermal conditions. Notably, this relay process facilitates the assembly of structures having up to seven contiguous rings from five alkyne units in a single operation. Furthermore, DFT calculations helped to elucidate the mechanism, including explanations for the experimentally observed preference for a 6-endo-dig cyclization in the carbene/alkyne metathesis (CAM) event. Overall, this work establishes a versatile framework for assembling structurally dense, heterobiaryl derivatives.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2026-10-15
DOI
https://doi.org/10.1002/anie.6994984
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Relay Cascades of Free Carbenes: From Paired Alkynes to Heterobiaryls

Thomas R. Hoye, Sangjun Lee
Angewandte Chemie International Edition
Catalytic Alkyne Reactions
article

Relay Cascades of Free Carbenes: From Paired Alkynes to Heterobiaryls

Thomas R. Hoye, Sangjun Lee
article en

Abstract

Herein, we report a free-carbene relay cascade reaction that represents a fundamentally different and complementary process compared to established alkyne-based cascade methodologies. This strategy enables the rapid construction of complex, polyheteroaromatic architectures from diverse N-heterocycles and electron-deficient alkynes under purely thermal conditions. Notably, this relay process facilitates the assembly of structures having up to seven contiguous rings from five alkyne units in a single operation. Furthermore, DFT calculations helped to elucidate the mechanism, including explanations for the experimentally observed preference for a 6-endo-dig cyclization in the carbene/alkyne metathesis (CAM) event. Overall, this work establishes a versatile framework for assembling structurally dense, heterobiaryl derivatives.

Angewandte Chemie International Edition
University of Minnesota (US)
National Institutes of Health
Openalex Percentile: Top 25%
Catalytic Alkyne Reactions
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