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DOI: 10.1055/a-1941-2205
Improvements in Efficiency and Selectivity for C–F Bond Halogen-Exchange Reactions by Using Boron Reagents
Abstract
The use of boron Lewis acids as instigators of bond cleavage offers a number of synthetic possibilities. A unique feature of this class of reagents is the ability to functionalize otherwise inert C–F bonds. We summarize notable developments in C–F bond halogen exchange using Lewis acidic boron reagents and we conclude by featuring our group’s advances in activating CF3 groups by using boron trihalides.
1 Introduction
2 Boron-Mediated Halogen Exchange
3 Mono-Selective C–F Activation
4 Conclusions
Key words
halogen exchange - boron trihalides - C–F bond activation - trifluoromethyl group activation - C–F functionalization - Lewis acidsPublikationsverlauf
Eingereicht: 16. August 2022
Angenommen nach Revision: 12. September 2022
Accepted Manuscript online:
12. September 2022
Artikel online veröffentlicht:
25. November 2022
© 2022. Thieme. All rights reserved
Georg Thieme Verlag KG
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For boron tribromide as a reagent, see:
For alternative types of boron-catalyzed processes, see:
For a general overview of C–F activation strategies, see: