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1,4 Reduction of a conjugated iminoenolether with complex metal hydrides

✍ Scribed by S.W. Breuer; Paul Yates

Publisher
Elsevier Science
Year
1969
Tongue
French
Weight
102 KB
Volume
10
Category
Article
ISSN
0040-4039

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✦ Synopsis

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

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