| License: Creative Commons Attribution 4.0 (1MB) |
- URN to cite this document:
- urn:nbn:de:bvb:355-epub-775560
- DOI to cite this document:
- 10.5283/epub.77556
Abstract
Phosphine–boranes have garnered growing interest for their potential in catalysis and as building blocks for inorganic polymers. While various synthetic methods exist, flexibility to introduce diverse substituents on the P centers remains limited. Our group reported routes to monoalkylated phosphanylboranes starting from primary phosphanylboranes or sodium phosphide. In this work, we extend ...

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