Claisen rearrangement of amide oxime–dimethyl acetylenedicarboxylate adducts as a route to imidazolinones
- 1 January 1971
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society D: Chemical Communications
- No. 13,p. 664
- https://doi.org/10.1039/c29710000664
Abstract
Pyrolysis of the vinyl ether adducts obtained by condensation of arylamide oximes and dimethyl acetylene dicarboxylate affords a new class of substituted imidazolinones, probably by a Claisen-type rearrangement with subsequent cyclisation.Keywords
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