A new trinor-guaiane sesquiterpene named clavukerin C (2), having a hydroperoxy function, was isolated together with clavukerin A (1), clavukerin B (3), and bicyclogermacrene (4) from the Okinawan soft coral (stolonifer) Clavularia koellikeri. The absolute stereo-structure of clavukerin C (2) was elucidated. Clavukerin B (3) was found to be identical with or antipodal to trinoranastreptene, which was previously reported as a liverwort metabolite. © 1984, The Pharmaceutical Society of Japan. All rights reserved.
CITATION STYLE
Kobayashi, M., Son, B. W., Kitagawa, I., & Kyogoku, Y. (1984). Clavukerin C, A new trinor-guaiane sesquiterpene having a hydroperoxy function, from the okinawan soft coral: Clavularia koellikeri. Chemical and Pharmaceutical Bulletin, 32(4), 1667–1670. https://doi.org/10.1248/cpb.32.1667
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