Issue 5, 1994

Studies on fused pyrimidine derivatives. Part 13. Thermal ene reaction of 6-(alk-2-enylamino)-5-[(substituted imino)methyl]-1,3-dimethylpyrimidine-2,4(1H,3H)-diones leading to pyrimido[4,5-b]azepines

Abstract

6-(Alk-2-enylamino)-1,3-dimethyl-5-[(substituted imino)methyl]pyrimidine-2,4(1H,3H)-diones, obtained from 6-(alk-2-enylamino)-5-formyl-1,3-dimethylpyrimidine-2,4(1H,3H)-diones 1 and primary amines, participate in the intramolecular ene reaction (Type III) leading to pyrimido[4,5-b]azepine derivatives.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1994, 565-570

Studies on fused pyrimidine derivatives. Part 13. Thermal ene reaction of 6-(alk-2-enylamino)-5-[(substituted imino)methyl]-1,3-dimethylpyrimidine-2,4(1H,3H)-diones leading to pyrimido[4,5-b]azepines

T. Inazumi, E. Harada, T. Mizukoshi, Y. Kuroki, A. Kakehi and M. Noguchi, J. Chem. Soc., Perkin Trans. 1, 1994, 565 DOI: 10.1039/P19940000565

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