Halogenated secondary metabolites from Laurencia obtusa

Aydogmus Z., Imre S., Ersoy L., Wray V.

NATURAL PRODUCT RESEARCH, vol.18, no.1, pp.43-49, 2004 (Journal Indexed in SCI) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 18 Issue: 1
  • Publication Date: 2004
  • Doi Number: 10.1080/1057563031000122086
  • Title of Journal : NATURAL PRODUCT RESEARCH
  • Page Numbers: pp.43-49

Abstract

A new sesquiterpene (1), and a halogenated C-15 acetogenin (2), a stereoisomer of neoisoprelaurefucin were isolated from Laurencia obtusa. Four known compounds laurencienyne (3), rogiolenyne B (4), obtusenol (5), and (3E)-dactomelyne (6) were also isolated from this alga. Rogiolenyne B (4) and (3E)-dactomelyne (6) were found for the first from this species. The structures of these compounds were elucidated by spectroscopic methods. The unambiguous assignments of the H-1 and C-13 NMR spectral data of (5) and C-13 NMR data of (6) were also reported for the first time.