Reactions of Group IV organometallic compounds. Part XI. Some insertion reactions of alkylsilyl and alkylstannyl sulphides
作者:Kenji Itoh、Kimishige Matsuzaki、Yoshio Ishii
DOI:10.1039/j39680002709
日期:——
Reaction of trimethylsilyl sulphide with phenyl isocyanate gives a 1 : 1 insertion product, but subsequent insertion of phenyl isocyanate takes place readily in the case of trialkylstannyl sulphide, to produce triphenyl isocyanurate. When chloral is used as a reactant for trialkyltin sulphides, substitution of all three chlorine atoms occurs, to afford trialkyltin chloride and (RS)3C·CHO, although