Chamigrane metabolites from a Jamaican variety of laurencia obtusa

Phytochemistry

Volumn 26, Issue 4, 1987, Pages 1053-1057

  Brennan, Mary R ^a   Erickson, Karen L ^a   Minott, Donna A ^a,b   Pascoe, Keith O ^a,b  

^a CLARK UNIVERSITY   (United States)

^b UNIVERSITY OF THE WEST INDIES   (Jamaica)

Author keywords

halochamigrenes.; Laurencia obtusa; marine algae; Rhodomelaceae; sesquiterpenes

Indexed keywords

EID: 0001654357     PISSN: 00319422     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0031-9422(00)82349-3     Document Type: Article

References (26)

1. Epilaurallene, a new nonterpenoid C15-bromoallene from the red alga Laurencia nipponica Yamada.
2. Evidence for the biogenesis of halogenated chamigrenes from the red alga laurencia obtusa
3. Carbon-13 NMR application to Laurencia polyhalogenated sesquiterpenes
4. Halogenated terpenoids. XX. The seven monochlorocineoles