Nepetanudone, a dimer of the alpha-pyrone 5,9-dehydronepetalactone


KOKDIL G., Topcu G. , KRAWIEC M., WATSON W.

JOURNAL OF CHEMICAL CRYSTALLOGRAPHY, vol.28, no.7, pp.517-519, 1998 (Journal Indexed in SCI) identifier

  • Publication Type: Article / Article
  • Volume: 28 Issue: 7
  • Publication Date: 1998
  • Doi Number: 10.1023/a:1023287804704
  • Title of Journal : JOURNAL OF CHEMICAL CRYSTALLOGRAPHY
  • Page Numbers: pp.517-519

Abstract

The title compound C20H24O4 crystallizes in the orthorhombic space group P2(1)2(1)2, with a = 10,245(3), b = 17.103(3), c = 9.879(3) Angstrom, D-c = 1.260 g cm(-3), and Z = 4. Nepetanudone is postulated to be formed by a [4 + 4] cycloaddition of two 5,9-dehydronepetalactone moieties to give an asymmetric dimer in which each pair of atoms is magnetically nonequivalent. The compound was recovered from extracts of Nepeta nuda ssp. albiflora.