Issue 20, 1972

Photochemical reactivity of 2,4-dimethyl-1,2,4-triazine-3,5-(2H)-dione (1,3-dimethyl-6-azauracil)

Abstract

In contrast to the general photochemical unreactivity of the 6-aza-analogues of uracils and thymines, 2,4-dimethyl-1,2,4-triazine-3,5(2H)-dione undergoes acetone-sensitized regioselective cycloaddition to ethyl vinyl ether yielding labile azetidine cycloadducts.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 1144-1145

Photochemical reactivity of 2,4-dimethyl-1,2,4-triazine-3,5-(2H)-dione (1,3-dimethyl-6-azauracil)

J. A. Hyatt and J. S. Swenton, J. Chem. Soc., Chem. Commun., 1972, 1144 DOI: 10.1039/C39720001144

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