Se‐Phenyl selenocarboxylates have been conveniently prepared from (phenylseleno)acetylenes by treatment with p‐toluenesulfonic acid monohydrate in dichloromethane. This easy conversion is compatible with a broad range of oxygen‐ and nitrogen‐containing functional groups. The Se‐phenyl selenocarboxylates were easily converted into the corresponding esters and amides. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)
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Tiecco et al. (2004) studied this question.
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