Reactions of PAr /B(C F ) (Ar=o-Tol, Mes, Ph) FLPs with diethyl azodicarboxylate (DEAD) afford the corresponding FLP addition products 1-3 in which P-N and B-O linkages are formed. In contrast, the reaction of BPh , PPh and DEAD gave product 4 where P-N and N-B linkages were confirmed. In all cases, other binding modes were computed to be both higher in energy and readily distinguishable by P and B NMR parameters. These data illustrate the influence of steric demands and electronic structures on the nature of the products of FLP reactions with DEAD.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796924 | PMC |
http://dx.doi.org/10.1002/chem.202201701 | DOI Listing |
Chemistry
September 2022
Institute of Drug Discovery Technology, Ningbo University, 315211, Zhejiang, P. R. China.
Reactions of PAr /B(C F ) (Ar=o-Tol, Mes, Ph) FLPs with diethyl azodicarboxylate (DEAD) afford the corresponding FLP addition products 1-3 in which P-N and B-O linkages are formed. In contrast, the reaction of BPh , PPh and DEAD gave product 4 where P-N and N-B linkages were confirmed. In all cases, other binding modes were computed to be both higher in energy and readily distinguishable by P and B NMR parameters.
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