6,7-Dimethyl-4-methylthiopteridine (IV) resembles 6-methylthiopurine (I) in its dipole moment, and both compounds undergo alkylation in the pyrimidine ring, para to the thioether group. However, in contrast to the purine (I), the pteridine (IV) is readily amenable to thiohydrolysis, presumably under the influence of the π-deficient pyrazine ring.
Z. Neiman, F. Bergmann and H. Weiler-Feilchenfeld, J. Chem. Soc. C, 1969, 114 DOI: 10.1039/J39690000114
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...