The Molecular Rearrangement of Alpha, Beta-Unsaturated Ethers1
WM Lauer, MA Spielman
Index: Lauer; Spielman Journal of the American Chemical Society, 1933 , vol. 55, p. 4923,4927
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Citation Number: 9
Abstract
It has long been known that certain a, P-unsaturated ethers rearrange on heating to form ketones. For the first example we are indebted to Clai~ en,~ who found that a-ethoxystyrene readily forms phenyl propyl ketone “on short superheating such as boiling for a few hours under two atmospheres' pressure.” Only a few such rearrangements have been re-~ orded,~ and the reaction is not general, since ethyl/3-ethoxycrotonate, a-methoxymesityl oxide and ...
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