Issue 23, 1978

Reduction of α,α′-dibromoketones by ultrasonically dispersed mercury in some aliphatic ketone solvents. A convenient synthesis of 4-isopropylidene-1,3-dioxolans

Abstract

Reduction of 2,4-dibromo-2-4-dimethylpentan-3-one by finely dispersed mercury in ketonic solvents provides a simple synthesis of the 4-isopropylidene-5,5-dimethyl-1,3-dioxolan ring system.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1978, 1040-1041

Reduction of α,α′-dibromoketones by ultrasonically dispersed mercury in some aliphatic ketone solvents. A convenient synthesis of 4-isopropylidene-1,3-dioxolans

A. J. Fry, G. S. Ginsburg and R. A. Parente, J. Chem. Soc., Chem. Commun., 1978, 1040 DOI: 10.1039/C39780001040

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