Issue 24, 1985

Intramolecular γ C–H insertion vs. olefin cycloaddition in 4-methylene-2-adamantylidene and 8-methylene-2-noradamantylidene

Abstract

8-Methylene-2-noradamantylidene inserts readily into the γ C–H bond giving 6-methylene-2,4-didehydro-noradamantane rather than the olefin-cycloaddition product, while its higher homolouge 4-methylene-2-adamantylidene reacts exclusively by intramolecular cycloaddition to the olefinic bond yielding 2,4-methano-2,4-didehydroadamantane, a [3.1.1.]propellane.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 1830-1831

Intramolecular γ C–H insertion vs. olefin cycloaddition in 4-methylene-2-adamantylidene and 8-methylene-2-noradamantylidene

Z. Majerski, Z. Hameršak and K. Mlinarić-Majerski, J. Chem. Soc., Chem. Commun., 1985, 1830 DOI: 10.1039/C39850001830

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