Issue 14, 1995

The synthesis of novel 3,4-dihydro-1,2,5,7,4-tetroxazocine derivatives via extended [3 + 3 + 2] cycloaddition reactions between a carbonyl oxide, a nitrone and an aldehyde

Abstract

Ozonolysis of acenaphthylene in the presence of a nitrone 2 yields the corresponding polycyclic peroxide 5 containing the novel dihydro-1,2,5,7,4-tetroxazocine ring system; the structure of the crystalline adduct 5a has been unambiguously determined by X-ray crystallographic analysis.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 1469-1470

The synthesis of novel 3,4-dihydro-1,2,5,7,4-tetroxazocine derivatives via extended [3 + 3 + 2] cycloaddition reactions between a carbonyl oxide, a nitrone and an aldehyde

S. Satake, Y. Ushigoe, M. Nojima and K. J. McCullough, J. Chem. Soc., Chem. Commun., 1995, 1469 DOI: 10.1039/C39950001469

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