The ozonolysis of azoles was investigated, and the products formed via a 1,2-addition of ozone were the main ones obtained. In particular, 2,5-disubstituted oxazoles (2) were treated with an excess of an ozone–oxygen stream to give the corresponding acid anhydrides (6) quantitatively. This reaction should be useful for the preparation of the mixed anhydrides (6) in good yield at low temperature.
C. Kashima, S. Hibi, K. Harada and Y. Omote, J. Chem. Soc., Perkin Trans. 1, 1988, 529 DOI: 10.1039/P19880000529
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.
Please wait while we load your content...