EXPERIMENTS DIRECTED TOWARDS THE SYNTHESIS OF ANTHRACYCLINONES .18. NOVEL DIOXEPINS FROM THE BORON-TRIFLUORIDE CATALYZED CYCLIZATION OF METHALLYL ANTHRAQUINONE ACETALS

Authors
CAMBIE RC HOLROYD SE RUTLEDGE PS WOODGATE PD
Citation
Rc. Cambie et al., EXPERIMENTS DIRECTED TOWARDS THE SYNTHESIS OF ANTHRACYCLINONES .18. NOVEL DIOXEPINS FROM THE BORON-TRIFLUORIDE CATALYZED CYCLIZATION OF METHALLYL ANTHRAQUINONE ACETALS, Australian Journal of Chemistry, 46(5), 1993, pp. 703-712
Citations number
11
Categorie Soggetti
Chemistry
Journal title
Australian Journal of Chemistry → ACNP
ISSN journal
00049425
Volume
46
Issue
5
Year of publication
1993
Pages
703 - 712
Database
ISI
SICI code
0004-9425(1993)46:5<703:EDTTSO>2.0.ZU;2-X
Abstract
Boron trifluoride mediated cyclizations of ortho-methallyl-substituted homochiral anthraquinone acetals yield novel dioxepins, which are pro bably formed via free carbocation intermediates.