UNPRECEDENTED FORMATION OF A CYCLIC TETRAMER FROM THE ACIDOLYSIS OF INDENE OZONIDE - ISOLATION AND CHARACTERIZATION OF A NOVEL DODECAOXACYCLOICOSANE DERIVATIVE

Authors
MCCULLOUGH KJ TESHIMA K NOJIMA M
Citation
Kj. Mccullough et al., UNPRECEDENTED FORMATION OF A CYCLIC TETRAMER FROM THE ACIDOLYSIS OF INDENE OZONIDE - ISOLATION AND CHARACTERIZATION OF A NOVEL DODECAOXACYCLOICOSANE DERIVATIVE, Journal of the Chemical Society, Chemical Communications, (11), 1993, pp. 931-933
Citations number
14
Categorie Soggetti
Chemistry
Journal title
Journal of the Chemical Society, Chemical Communications → ACNP
ISSN journal
00224936
Issue
11
Year of publication
1993
Pages
931 - 933
Database
ISI
SICI code
0022-4936(1993):11<931:UFOACT>2.0.ZU;2-8
Abstract
Treatment of indene ozonide with chlorosulfonic acid in methylene chlo ride at 0-degrees-C affords a crystalline tetramer of the ozonide, the structure of which is shown by X-ray crystallographic analysis to con tain a novel 20-membered dodecaoxacycloicosane ring system.