Issue 13, 1971

Claisen rearrangement of amide oxime–dimethyl acetylenedicarboxylate adducts as a route to imidazolinones

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.

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 664-664

Claisen rearrangement of amide oxime–dimethyl acetylenedicarboxylate adducts as a route to imidazolinones

N. D. Heindel and M. C. Chun, J. Chem. Soc. D, 1971, 664 DOI: 10.1039/C29710000664

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements