Abstract
Derivatisation reactions of 2-chloro-3-dichlorophosphanyl-1-methyl-1.3.2-diazaphosphorinane 1 with protic nucleophiles like HNEt2, CH3OH, C2H5OH and the Franz-reagent NEt33HF forming the substituted N-phosphanyldiazaphosphorinanes 2-12 are described. The preferential nucleophilic attack on the exocyclic phosphanyl group of 1 in partial replacement reactions is discussed by means of 31P-, 1H- and 13C-NMR data.