Issue 0, 1969

N- and N′-aryl substitution in benzamidines

Abstract

N-Phenyl substitution of amino- and imino-groups in benzamidines is shown to reduce basic strength by factors of ca. 10 and 1000, respectively. The configuration of the imino-N-phenyl ring is discussed. The structure of the predominant tautomer of N-(3-diethylaminopropyl)-N′-phenylbenzamidine is indicated.

Article information

Article type
Paper

J. Chem. Soc. B, 1969, 66-67

N- and N′-aryl substitution in benzamidines

J. A. Smith and H. Taylor, J. Chem. Soc. B, 1969, 66 DOI: 10.1039/J29690000066

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