Evidence from studies on reactivity, linear free energy relationships, trapping with an amine, and activation data indicates that the unprecedented anionic sulphonylamine (2) is involved in the alkaline hydrolysis of aryl sulphamates.
S. Thea, G. Cevasco, G. Guanti and A. Williams, J. Chem. Soc., Chem. Commun., 1986, 1582 DOI: 10.1039/C39860001582
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...