ArticleNature communications2025
Borylated strain rings synthesis via photorearrangements enabled by energy transfer catalysis.
Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
7 citing papers in PubMed.
- Redirecting radical phosphonylation via energy-transfer-enabled diradical rearrangement.Science advances · 2026Article
- Converting 1,1-Bisborylalkanes into 1,2-Bisborylalkanes Enabled by Iron Ligand-to-Metal Charge Transfer (LMCT) Photocatalysis.Angewandte Chemie (International ed. in English) · 2026Article
- (Poly)Borylated Species as Modern Reactive Groups toward Unusual Synthetic Applications.Angewandte Chemie (International ed. in English) · 2026Review
- Fused 3D boron heterocyclesChemical science · 2026Article
- Photochemical rearrangement of isonitriles via energy transfer catalysis.Nature communications · 2025Article
- The Curious Case of β-Boryl Triplet States.Trends in chemistry · 2025Article
- Synthesis of Borylated Orphaned Cyclopropanes through a Boron-Enabled Cycloisomerization Reaction.Journal of the American Chemical Society · 2025Article
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
Borylated carbocycles occupy a pivotal position as essential components in synthetic chemistry, drug discovery, and materials science. Herein, we present a photorearrangement that uniquely involves a boron atom enabled by energy transfer catalysis under visible light conditions. The boron functional group could be translocated through energy transfer mechanism and valuable borylated cyclopropane scaffolds could be generated smoothly. Furthermore, we showcase a 1,5-HAT (hydrogen atom transfer)/cyclization reaction, which is also enhanced by energy transfer catalysis excited by visible light. This method enables the synthesis of borylated cyclobutane frameworks. These boron-involved photorearrangement and cyclization reactions represent two techniques for synthesizing highly desirable borylated strained ring structures, which offering avenues for the synthesis of complex organic molecules with medicinal and material science applications.
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Registered trials
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.