“…The reactions of phosphorus-containing 2,6-di-tert-butyl-4methylene-2,5-cyclohexadienones with nucleophiles has been recognized as a convenient approach to prepare spatially hindered phenols containing phosphoryl fragments [2,3]. The stable dialkyl[(3,5-di-tert-butyl-4-oxo-2,5-cyclohexadienylidene)methyl]phosphonates readily react with nucleophiles to form the 1,6-addition products [2,4,5].…”