@article{oai:nagasaki-u.repo.nii.ac.jp:00008910,
 author = {Takamura, Kaoru and Matsuo, Hisami and Tanaka, Ayana and Tanaka, Junji and Fukuda, Tsutomu and Ishibashi, Fumito and Iwao, Masatomo},
 issue = {13},
 journal = {Tetrahedron},
 month = {Apr},
 note = {Total synthesis of the pyrrolic marine natural products lukianols A (1) and B (2) has been achieved using N-benzenesulfonyl-3,4-dibromopyrrole (3) as a common starting material. The key synthetic strategy developed is the combined bromine-directed lithiation and palladium-catalyzed cross-coupling of 3 to produce 3,4-diarylpyrrol-2-carboxylates. Regioselective iodination of the phenolic intermediate 24 was thoroughly investigated for the synthesis of lukianol B., Tetrahedron, 69(13), pp.2782-2788; 2013},
 pages = {2782--2788},
 title = {Total synthesis of the marine natural products lukianols A and B},
 volume = {69},
 year = {2013}
}