4.2 Article

Halogenated chamigrane sesquiterpenes from Laurencia okamurae

Journal

MAGNETIC RESONANCE IN CHEMISTRY
Volume 50, Issue 2, Pages 174-177

Publisher

WILEY-BLACKWELL
DOI: 10.1002/mrc.2870

Keywords

NMR; 1H NMR; 13C NMR; two-dimensional NMR; laurokamin A; laurokamin B; laurokamin C; Laurencia okamurae

Funding

  1. Shandong Province Natural Science Foundation [ZR2009BQ021]
  2. National Natural Science Foundation of China [41106136, 41106137]
  3. Chinese Academy of Sciences [KZCX2-YW-QN209, KZCX2-YW-225]
  4. Foundation of the Chinese Academy of Sciences

Ask authors/readers for more resources

Three new halogenated chamigrane sesquiterpenes, laurokamin A (1), laurokamin B (2), and laurokamin C (3), and four known halogenated chamigrane sesquiterpenes, 10-bromo-alpha-chamigrene (4), 10-bromo-beta-chamigrene (5), 2,10-dibromo-3-chloro-beta-chamigrene (6), and obtusane (7), were isolated from the marine red alga Laurencia okamurae collected from the coast of Rongcheng, China. The structures of these compounds were unambiguously identified by one- and two-dimensional NMR and mass spectroscopic methods. The antimicrobial activity of compounds 13 was evaluated. Copyright (C) 2012 John Wiley & Sons, Ltd.

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