Synthesis of five- and six-membered cyclic organic peroxides: Key transformations into peroxide ring-retaining products

97Citations
Citations of this article
72Readers
Mendeley users who have this article in their library.

Abstract

The present review describes the current status of synthetic five and six-membered cyclic peroxides such as 1,2-dioxolanes, 1,2,4- trioxolanes (ozonides), 1,2-dioxanes, 1,2-dioxenes, 1,2,4-trioxanes, and 1,2,4,5-tetraoxanes. The literature from 2000 onwards is surveyed to provide an update on synthesis of cyclic peroxides. The indicated period of time is, on the whole, characterized by the development of new efficient and scale-up methods for the preparation of these cyclic compounds. It was shown that cyclic peroxides remain unchanged throughout the course of a wide range of fundamental organic reactions. Due to these properties, the molecular structures can be greatly modified to give peroxide ring-retaining products. The chemistry of cyclic peroxides has attracted considerable attention, because these compounds are used in medicine for the design of antimalarial, antihelminthic, and antitumor agents. © 2014 Terent'ev et al.

Cite

CITATION STYLE

APA

Terent’ev, A. O., Borisov, D. A., Vil, V. A., & Dembitsky, V. M. (2014, January 8). Synthesis of five- and six-membered cyclic organic peroxides: Key transformations into peroxide ring-retaining products. Beilstein Journal of Organic Chemistry. https://doi.org/10.3762/bjoc.10.6

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free