ArticleChemistryOpen2017
Convenient and General Zinc-Catalyzed Borylation of Aryl Diazonium Salts and Aryltriazenes under Mild Conditions.
Article in ChemistryOpen, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 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.
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Who cites it
6 citing papers in PubMed.
- Verdazyl Radical Organocatalysis Overcomes Chain-Propagation Limitations in Borylation of Arenediazonium Salts.The Journal of organic chemistry · 2026Article
- Recent trends in the chemistry of Sandmeyer reaction: a review.Molecular diversity · 2022Review
- New avenues for C-B bond formationChemical science · 2019Review
- Metal-Free Radical Borylation of Alkyl and Aryl Iodides.Angewandte Chemie (International ed. in English) · 2018Article
- Transition Metal-Free 1,2-Carboboration of Unactivated Alkenes.Journal of the American Chemical Society · 2018Article
- Convenient and General Zinc-Catalyzed Borylation of Aryl Diazonium Salts and Aryltriazenes under Mild Conditions.ChemistryOpen · 2017Article
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
A convenient and general zinc-catalyzed borylation of aryl diazonium salts and aryltriazenes has been developed. With bis- (pinacolato)diboron as the borylation reagent, aryldiazonium tetrafluoroborate salts and aryltriazenes were transformed into the corresponding arylboronates in moderate to excellent yields under mild conditions. As a convenient and practical methodology, no additional ligands, base, or any other additives are required here.
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Registered trials
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