Thermolysis of dibutyl(2-ethoxyethyl)stannane (4) in heptane at 150 de
grees C quantitatively provides the perbutylated cyclopolystannanes (B
u(2)Sn)(5) (1) and (Bu(2)Sn)(6) (2). Trapping experiments reveal that
this formal reductive-elimination process proceeds in a step-wise mann
er, involving the generation of a trivalent tin. intermediate that the
n undergoes an. unprecedented beta-elimination reaction.