ArticleThe Journal of organic chemistry2017
Method for Accessing Nitrogen-Containing, B-Heteroaryl-Substituted 2,1-Borazaronaphthalenes.
Article in The Journal of organic chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
What it found
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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
9 citing papers in PubMed.
- 1,2-Migratory ring expansion of a BN-naphthalene.Organic & biomolecular chemistry · 2025Article
- Modular synthesis of 1,2-azaborines via ring-opening BN-isostere benzannulation.Nature chemistry · 2024Article
- A Pyridyl-1,2-azaborine Ligand for Phosphorescent Neutral Iridium(III) Complexes.Inorganic chemistry · 2023Article
- Selectivity in the Elaboration of Bicyclic Borazarenes.Advanced synthesis & catalysis · 2021Article
- Synthesis and biological evaluation of an antibacterial azaborine retinoid isostereTetrahedron letters · 2021Article
- Synthesis and characterization of an unnatural boron and nitrogen-containing tryptophan analogue and its incorporation into proteins.Chemical science · 2019Article
- Four-coordinate triarylborane synthesisChemical science · 2018Article
- The State of the Art in Azaborine Chemistry: New Synthetic Methods and Applications.Journal of the American Chemical Society · 2018Review
- A modular route to boron doped PAHs by combining borylative cyclisation and electrophilic C-H borylation.Chemical science · 2017Article
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
The azaborine motif provides a mimic of aromatic systems through replacement of a C═C bond with a B-N bond. In particular, 2,1-borazaronaphthalenes, accessible through robust methods of synthesis and subsequent functionalization, afford an ideal platform to use for a variety of applications. However, the scope of substructures for this archetype has been limited by the lack of nitrogen-containing heteroaryls that can be incorporated within them. In this study, modified reaction conditions were developed to provide access to a wider range of substructures.
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Registered trials
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