Attempted halogenation of ambiphilic 1,2,3-benzodiazaborines: balancing Lewis acidity and Lewis basicity

Leonie Wüst, Tim Wellnitz, Krzysztof Radacki, Samuel Nees, Holger Braunschweig

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DOI: 10.1039/d6cc01072e
Published: 2026
Container: Chemical Communications
Publisher: Royal Society of Chemistry (RSC)
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1039/d6cc01072e,
  title = {Attempted halogenation of ambiphilic 1,2,3-benzodiazaborines: balancing Lewis acidity and Lewis basicity},
  author = {Leonie Wüst and Tim Wellnitz and Krzysztof Radacki and Samuel Nees and Holger Braunschweig},
  year = {2026},
  journal = {Chemical Communications},
  doi = {10.1039/d6cc01072e},
  url = {https://doi.org/10.1039/d6cc01072e}
}

RIS

TY  - JOUR
TI  - Attempted halogenation of ambiphilic 1,2,3-benzodiazaborines: balancing Lewis acidity and Lewis basicity
AU  - Leonie Wüst
AU  - Tim Wellnitz
AU  - Krzysztof Radacki
AU  - Samuel Nees
AU  - Holger Braunschweig
PY  - 2026
JO  - Chemical Communications
DO  - 10.1039/d6cc01072e
UR  - https://doi.org/10.1039/d6cc01072e
ER  -

APA

Wüst, L., Wellnitz, T., Radacki, K., Nees, S., & Braunschweig, H. (2026). Attempted halogenation of ambiphilic 1,2,3-benzodiazaborines: balancing Lewis acidity and Lewis basicity. Chemical Communications. https://doi.org/10.1039/d6cc01072e

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crossref · retrieved 2026-09-26T16:50:45.448Z