Issue 6, 1997
From the journal:

Journal of Chemical Research, Synopses

NH-Acidities of Some Sterically Hindered Ureas†

Ivan G. Pojarlieff,   Iva B. Blagoeva,   Bozhana P. Mikhova,   Ergun Atay  and  Anthony J. Kirby  

Abstract

Introduction of an N-methyl group in to ethyl N-methylhydantoate causes a fourfold decrease in the rate of base-catalysed exchange of the N-H proton; a second methyl group restores the rate to close to that of the N-unsubstituted hydantoate; the latter effect is observed for N-phenylhydantoates.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/A608619E
Article type
Paper

J. Chem. Res. (S), 1997, 220-221

Permissions

Request permissions

NH-Acidities of Some Sterically Hindered Ureas†

I. G. Pojarlieff, I. B. Blagoeva, B. P. Mikhova, E. Atay and A. J. Kirby, J. Chem. Res. (S), 1997, 220 DOI: 10.1039/A608619E

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.

Spotlight

Advertisements