Skip to main content
TetrahedronVolume 38, Issue 21, 1982, Pages 3163-3168

Circular dichroism of some cyclopropane ring containing 1,3-cyclo-5,10-seco-steroidal ketones(Article)

  Save all to author list
  • aDepartment of Chemistry, Faculty of Science, University of Belgrade, Belgrade
  • bRuhr University, Bochum, Germany

Abstract

Circular dichroism of the rearranged keto steroids 3 and 4, containing a condensed three and nine-membered ring system, shows that the conformation of the nine-membered ring is the same in solution as in the crystal; reduction of the kto group does not change this situation. CD also indicates that epimerization at C(5) in the pair 7 8 and the pair 11 12 leaves the cyclononanone ring conformation unchanged. © 1982.

Funding details

Funding sponsor Funding number Acronym
Verband der Chemischen IndustrieVCI
  • 1

    G.S. thanks the Deutsche Furschungsgemeinschaft and the Funds der Chemischen Industrie for financial support, and G. T.. The A.-von-Humboldt Foundation for a grant.

  • 2

    Acknowledgements--The authors from Belgrade are grateful to the Serbian Research Fund and to the Serbian Academy of Sciences and Arts for financial support.

  • ISSN: 00404020
  • CODEN: TETRA
  • Source Type: Journal
  • Original language: English
  • DOI: 10.1016/0040-4020(82)80053-7
  • Document Type: Article

  Mihailović, M.Lj.; Department of Chemistry, Faculty of Science, University of Belgrade,
© Copyright 2014 Elsevier B.V., All rights reserved.

Cited by 1 document

Kirk, D.N.
Steroids: Physical methods
(1984) Natural Product Reports
View details of this citation

SciVal Topic Prominence

Topic:
Prominence percentile: