ArticleOrganic letters2026
Cascade Synthesis of Structurally Diverse B-X-Doped Polycyclic Aromatic Hydrocarbons.
Article in Organic letters, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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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
5 authors.
Funding
Abstract
A modular, metal-free, cascade cyclization of functionalized enynes provides rapid access to structurally diverse boron-doped polycyclic aromatic hydrocarbons. The method simultaneously constructs the polycyclic framework and B-O, B-N, or C-B bonds while allowing straightforward boron functionalization. The alkene substitution pattern dictates the cyclization pathway, enabling selective formation of five- or six-membered rings. Photophysical studies reveal how structural variations govern the optical and fluorescence properties of these π-conjugated materials.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.