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Australian Journal of Chemistry Australian Journal of Chemistry Society
An international journal for chemical science
RESEARCH ARTICLE

Tropical Marine Algae. IV. Novel Metabolites From the Red Alga Laurencia implicata (Rhodophyta, Rhodophyceae, Ceramiales, Rhodomelaceae)

JC Coll and AD Wright

Australian Journal of Chemistry 42(10) 1685 - 1693
Published: 1989

Abstract

The marine alga Laurencia implicata afforded four new C15-lipid' type metabolites: (3Z,6Z,9Z)-12-bromo-5,13-epoxypentadeca-3,6,9-trien-1-yne (6) with an unprecedented 1-oxacyclodecane ring, (3Z,6Z,92)-13-bromo-5,12-epoxypentadeca-3,6,9-trien-1-yne (7) with a nine-membered ether ring, (3E,6S,7S,9S,10S,12S,13R)-10,12-dibromo-6,9:7,13-bisepoxy-pentadec-3-en-l-yne (8), in which a chlorine atom in the known compound chlorofucin (9) has been replaced by bromine, (1R*,4R*,6S*,7S*)-9-acetoxy-1,10,12-tribromo-4,7:6,13-bisepoxypentadeca-1,2-diene (11) and the closely related known metabolite neolaurallene (10). In addition, a brominated sesquiterpene (1'R*,3′R*)-2-(3?-bromo-1′,2′,2′-trimethylcyclopentyl-5-methylphenol (14), The 2′-hydroxy derivative of α- bromocuparene (15), was identified. Structural elucidation of all metabolites was based on high-field n.m.r. studies and comparison with known metabolites.

https://doi.org/10.1071/CH9891685

© CSIRO 1989

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