Issue 14, 1981

Synthesis of nitrosothioureas. 15N N.m.r. evidence for the formation of thionitrosyl compounds in the nitrosation of thioureas

Abstract

Nitrosothioureas may be prepared by treatment of thioureas with NaNO2 in 0·1 N HCl at –5 °C by direct N-nitrosation whereas 15N n.m.r. studies at –10 °C which employed specifically 15N-enriched compounds revealed the intermediacy of a thionitrosyl compound under more acidic conditions which gave the urea by hydrolysis.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 675-676

Synthesis of nitrosothioureas. 15N N.m.r. evidence for the formation of thionitrosyl compounds in the nitrosation of thioureas

J. W. Lown and S. M. S. Chauhan, J. Chem. Soc., Chem. Commun., 1981, 675 DOI: 10.1039/C39810000675

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