3-(1-tert-Butyldimethylsiloxyethyl)-4-phenylsulfinylazetidin-2-one reacted smoothly with various types of O-silylated ketene acetals and silylated enol ethers in the presence of a catalytic amount of zinc iodide to give the corresponding trans-4-substituted azetidin-2-ones in good yields. The latter compounds are key intermediates for the synthesis of carbapenems and 1β-methylcarbapenems.
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Kita et al. (1992) studied this question.
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