In contrast to 1,2-di-iodobenzene, photolysis of 5,6-di-iodo-1,3-dimethyluracil in benzene and in furan rapidly gives products derived from a radical intermediate and none derived from the corresponding pyrimidyne. 5-Iodo-1,3-dimethyluracil radical is believed to be the precursor of all the identified products. The scope and mechanism of these photoreactions are discussed.
R. D. Youssefyeh and L. Lichtenberg, J. Chem. Soc., Perkin Trans. 1, 1974, 2649 DOI: 10.1039/P19740002649
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...