ArticleACS omega2025
TBACN-Promoted Regioselective Cyanofunctionalization and Benzannulation: Enabling Access to Cyanoindolizine Scaffolds via Alkyne Cyclization.
Article in ACS omega, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
4 authors.
Funding
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Abstract
A novel and regioselective cyanofunctionalization-benzannulation cascade reaction has been developed, utilizing tetrabutylammonium cyanide (TBACN) as a practical and efficient cyanide source. This transformation provides streamlined access to a structurally diverse array of cyano-substituted indolizine scaffolds, which are valuable intermediates in the synthesis of nitrogen-containing heterocycles with potential pharmaceutical applications. The methodology employs readily available
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Registered trials
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