Oxidation of extremely overcrowded 1,2-thiagermacyclohex-4-ene derivatives
with m-chloroperbenzoic acid resulted in competitive formation of the ring
expanded 1,2,7-oxathiagermacyclohept-4-ene derivatives and the ring contrac
ted 1,2,3-oxathiagermacyclopentane derivatives. The latter reaction product
s are found to isomerize into the former ones very slowly at room temperatu
re not only in solution but also in the crystalline state.