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Thiazepine photochemistry. Ready 1,3-hydrogen shifts from a side-chain amide
Journal of the Chemical Society D: Chemical Communications Pub Date : , DOI:10.1039/C29710000988
Abstract

An unusual, thermally reversible, 1,3-hydrogen shift occurs during irradiation of 6-benzyloxycarbonyl-amino-2,3-dihydro-1,4-thiazepines (2, 3, and the corresponding sulphoxide and sulphone of 3b); this is a special case of imine-enamine tautomerism, arising from the singlet excited state.

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