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Updated: Feb 8, 2026

Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of PhosphorusI
Published on: November 22, 2016
Effects of diminished steric protection at phosphorus on stability and reactivity of oxaphosphirane complexes
J Fassbender1, G Schnakenburg, A Espinosa Ferao
1Institut für anorganische Chemie der Universität Bonn, Gerhard-Domagk-Straße 1, 53121 Bonn, Germany. r.streubel@uni-bonn.de.
Abstract:
Readily available P-tBu substituted Li/Cl phosphinidenoid complexes react with carbonyl compounds to furnish sterically almost unhindered oxaphosphirane complexes that reveal new and surprisingly facile intra- and intermolecular ring expansion reactions. 1,3,2-Dioxaphosphole complex formation is explained by DFT calculations through diastereoselective carbonyl group-induced ring cleavage of an oxaphosphirane intermediate.
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