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January 1, 1972Journal of the Chemical Society Chemical Communications20 citations

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

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JHJohn A. HyattJSJohn S. Swenton

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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.

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Cite This Study

Hyatt et al. (1972) studied this question.

synapsesocial.com/papers/69df3f8635659245ec6146cehttps://doi.org/10.1039/c39720001144
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