Abstract
Diethyl(trimethylsilyl)phosphane 1 reacts with the conjugated carbonyl moiety of 2-benzal-1-indanones 2–6 to afford exclusively 1,4-adducts 2a–6a. Subsequent oxydation or sulfuration of most of the adducts leads to the corresponding phosphane oxides or sulfides. Further hydrolysis or reaction with HCl involves the desilylation with the formation of new (thio)phosphorylated ketones or phosphonium salts.