Issue 19, 1993

Formation of a 1,3-dipolar nitro addition product from the photochemical reaction of 1,2-dimethylnaphthalene and tetranitromethane

Abstract

The photochemical reaction between tetranitromethane and 1,2-dimethylnaphthalene gives, among other adducts, a product of internal 1,3-dipolar cycloaddition of a nitro group from the trinitromethyl group across the 1,2-double bond of the primary adduct, 1,2-dimethyl-r-3-nitro-4-trinitrometnyl-3,4-dihydronaphthalene.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 1513-1514

Formation of a 1,3-dipolar nitro addition product from the photochemical reaction of 1,2-dimethylnaphthalene and tetranitromethane

C. P. Butts, J. L. Calvert, L. Eberson, M. P. Hartshorn and W. T. Robinson, J. Chem. Soc., Chem. Commun., 1993, 1513 DOI: 10.1039/C39930001513

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