1,4 Reduction of a conjugated iminoenole
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S.W. Breuer; Paul Yates
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Article
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1969
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Elsevier Science
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French
β 102 KB
In the course of synthetic study we prepared the'enamine from dimedone and bensylaminel and reacted it with ethyl iodide, As expected2, the 0-ethylated product (I), an iminoenolether, was formed, As this compound is the vinylogue of an imidate, we wished to compare some of