References
- Biswas, S., Ghosh, A. and Kurosawa, E., Stereocontrolled synthesis of (\pm)debromoalysm, (\pm)aplysin, (\pm)debromoaplysinol, (\pm)aplysonol, and (\pm) isoaplysinol, J. Org. Chem., 55, 3498-3502 (1990) https://doi.org/10.1021/jo00298a022
- Blunt, J. W., Lake, R. J., Munro, M. H. G., Sesquiterpenes from the marine red alga Laurencia distichophylla. Phytochem., 23, 1951-1954 (1984) https://doi.org/10.1016/S0031-9422(00)84948-1
- Crews, P. and Selover, S. J., Comparison of the sesquiterpenes from the seaweed Laurencia pacifica and its epiphyte Erythrocystis saccata. Phytochem., 25, 1847-1852 (1986) https://doi.org/10.1016/S0031-9422(00)81160-7
- Hay, M.E. and Fenical, W., Gustafson, K., Chemical defence against diverse coral-reef herbivores. Ecology, 68, 1581-1591 (1987) https://doi.org/10.2307/1939850
- Harrowven, D. C., Lucas M. C. and Howes P. D., The synthesis of a natural product family: from debromoisolauhnterol to the aplysins. Tetrahedron, 57, 791-804 (2001) https://doi.org/10.1016/S0040-4020(00)01055-3
- Irie, T., Suzuki, M., Kurata, K. and Hayakawa, Y, Constituents of marine plants. XII. Isolation of aplysin, debromoaplysm, and aplysinol from Laurencia okamurai. Bull. Chem. Soc. Jap., 42, 843-844 (1964) https://doi.org/10.1246/bcsj.42.843
- Irie, T., Suzuki, M., Kurosawa, E. and Masamune, T., Lauiinterol and debromolauiinterol, constituents from Laurencia intermedia, Tetrahedron Lett., 17, 1837-1840 (1966)
- Irie, T., Suzuki, M., Kurosawa, E. and Masamune, T, Consdtuents from marine plants. XVI. Launnterol, debromolaurinterol, and isolauhnterol, constituents of Laurencia intermedia. Tetrahedron, 26, 3271-3277 (1970) https://doi.org/10.1016/S0040-4020(01)92906-0
- Kurata, K., Taniguchi, K., Agatsuma, Y and Suzuki, M. Diterpenoid feeding-deterrents from Laurencia saitoi. Phytochem. 47, 363-369 (1998) https://doi.org/10.1016/S0031-9422(97)00461-5
- McMillan, J.A., Paul, I.C., Caccamese, S. and Rmehart Jr K. R.,. Aplysinol from Laurencia decidua: crystal structure and Absolute stereochemistry, Tetrahedron Lett., 17, 4219-4222 (1976) https://doi.org/10.1016/0040-4039(76)80078-0
- Monsks, A., Scudiro, D., Skehan, R, Shoemaker, R., Paull, K., Visdca D., Hose, C., Langley, J., Cronise, R, Vaigro-Wolff, A., Gray-Goodrich, M., Campbell H., Mayo J. and Booyd M., Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines. J. Natl. Cancer Inst. 83, 757-766 (1991) https://doi.org/10.1093/jnci/83.11.757
- Ohta, K. and Takagi, M., Halogenated sesquiterpenes from the marine red alga Marginisporum aberrans. Phytochem., 16, 1062-1063 (1977) https://doi.org/10.1016/S0031-9422(00)86731-X
- Selover, S. J., Crews, P. and Kylinone, A new sesquiterpene skeleton from the marine alga Laurencia pacifica. J. Org. Chem., 45, 69-72 (1980) https://doi.org/10.1021/jo01289a015
- Shizuri, Y., Yamada, K. and Yamada, A.,Laurequinone, a cyclolaurane sesquiterpene from the red alga Laurenda nidifica. Phytochem., 23, 2672-2673 (1984) https://doi.org/10.1016/S0031-9422(00)84124-2
- Suzuki, M. and Kurosawa, E. New bromo compounds from Laurencia glandulifera kiitzing, Tetrahedron Lett., 17, 4817-4818 (1976) https://doi.org/10.1016/S0040-4039(00)78918-0
- Vairappan, C. S., Suzyki, S., Abe, T. and Masuda, M., Halogenated metabolites with antibactenal from the Okinawan Laurencia species. Phytochem., 58, 517-523 (2001) https://doi.org/10.1016/S0031-9422(01)00260-6
- Winkler, L. R., Tilton, B. E. and Hardinge, M. G., A cholmergic agent extracted from sea hares. Arch. Intern. Pharmacodyn., 137, 76-83 (1962)
- Yamamura, S. and Hirata, Y., Structure of aplysin and aplysinol, naturally occurring bromocompounds. Tetrahedron, 19, 1485-1496 (1963) https://doi.org/10.1016/S0040-4020(01)99222-1