Mutagenic N-acyloxy-N-alkoxybenzamides undergo SN2 reactions at the amide nitrogen with N-methylaniline and ring-substituted anilines in reactions modelling the possible mode of interaction between the mutagens and nucleic acids and which may be responsible for their biological activity.
J. J. Campbell and S. A. Glover, J. Chem. Res. (S), 1999, 474 DOI: 10.1039/A903555I
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...