@article{oai:nagasaki-u.repo.nii.ac.jp:00018290,
 author = {Fujikawa, Naotaka and Ohta, Takeshi and Yamaguchi, Tomohiro and Fukuda, Tsutomu and Ishibashi, Fumito and Iwao, Masatomo},
 issue = {4},
 journal = {Tetrahedron},
 month = {Jan},
 note = {Total synthesis of cytotoxic marine alkaloids, lamellarins D, L, and N, has been achieved by using Hinsberg-type pyrrole synthesis and palladium-catalyzedSuzuki-Miyaura coupling of the 3,4-dihydroxypyrrole bistriflate 6 as the key reactions.The total yields of lamellarins D, L, and N from the common intermediate 6 are 54, 58, and 50%, respectively., Tetrahedron, 62(4), pp.594-604;2006},
 pages = {594--604},
 title = {Total synthesis of lamellarins D, L, and N},
 volume = {62},
 year = {2006}
}