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
三甲基甲硅烷基硫醚与异氰酸苯酯的反应生成1:1的插入产物,但是在三烷基锡烷基硫醚的情况下,异氰酸苯酯的随后插入很容易发生,从而生成异氰脲酸三苯酯。当将氯醛用作三烷基锡硫化物的反应物时,尽管在三烷基甲硅烷基硫化物的情况下获得了简单的插入产物,但所有三个氯原子都被取代,从而得到三烷基氯化锡和(RS)3 C·CHO。β-丙内酯的烷基-氧键裂解已选择性地与Si-S化合物反应。