Issue 1, 1983

(1α and 1β)Methyl-1,1a,2,3,4,5-hexahydro-11H-azirino-[1′2′:2,3][1,2]diazocino[8,1-b]quinazolin-11-one: preference for a trans-fused aziridine in an eight-membered ring

Abstract

Intramolecular trapping of the nitrenes from oxidation of cis- and trans-2-(hept-2-en-7-yl)-3-amino-quinazolinones (1) and (3) gives the aziridines (2) and (4) respectively; in solution at room temperature (4) contains a mixture of nitrogen invertomers with the major invertomer having a trans-aziridine ring fusion, the latter being the only form present in the crystalline state.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 22-23

(1α and 1β)Methyl-1,1a,2,3,4,5-hexahydro-11H-azirino-[1′2′:2,3][1,2]diazocino[8,1-b]quinazolin-11-one: preference for a trans-fused aziridine in an eight-membered ring

R. S. Atkinson and K. L. Skinner, J. Chem. Soc., Chem. Commun., 1983, 22 DOI: 10.1039/C39830000022

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