Unprecedented formation of a cyclic tetramer from the acidolysis of indene ozonide. Isolation and characterisation of a novel dodecaoxacycloicosane derivative

Kevin J. McCullough, Koichi Teshima, Masatomo Nojima

Research output: Contribution to journalArticle

Abstract

Treatment of indene ozonide with chlorosulfonic acid in methylene chloride at 0 °C affords a crystalline tetramer of the ozonide, the structure of which is shown by X-ray crystallographic analysis to contain a novel 20-membered dodecaoxacycloicosane ring system.

Original languageEnglish
Pages (from-to)931-933
Number of pages3
JournalJournal of the Chemical Society, Chemical Communications
Issue number11
DOIs
Publication statusPublished - 1993

Fingerprint Dive into the research topics of 'Unprecedented formation of a cyclic tetramer from the acidolysis of indene ozonide. Isolation and characterisation of a novel dodecaoxacycloicosane derivative'. Together they form a unique fingerprint.

  • Cite this