Abstract
A stannylene acetal, in the presence of CsF, is able to cleave both aromatic and aliphatic acetates rapidly and efficiently under room temperature. Control experiments indicate that both the stannylene acetal and CsF are required and play significant roles in the deacetylation process. Thus, it is likely that the tin-based alkoxide anion generated by a stannylene acetal and CsF is responsible for deacetylation.
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