Abstract
Abstract A convenient method for synthesis of benzisoselenazol-3(2H)-ones substituted on the nitrogen atom with (polyhydroxy)alkyl or adenosinyl group is presented. It is based on the tandem acylation–selenenylation of primary amino group in aminopolyols or adenosine with 2-(chloroseleno)benzoyl chloride. The process is selective because oxygen nucleophiles (hydroxy groups) remained unreactive in the reaction conditions.
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