@article{oai:nagasaki-u.repo.nii.ac.jp:00004192,
 author = {Fukuda, Tsutomu and Sato, Daichi and Iwao, Masatomo},
 issue = {4},
 journal = {HETEROCYCLES},
 month = {},
 note = {A modular synthesis of the marine natural products lamellarins has been developed. The key reactions utilized are C3-selective Vilsmeier-Haack formylation followed by iterative bromination/cross-coupling of the 5,6-dihydropyrrolo[2,1-a]isoquinoline core. The 1,2-diaryl-5,6-dihydropyrrolo[2,1-a]isoquinoline-3-carbaldehyde thus synthesized was readily converted to the lamellarin skeleton by mean of palladium-catalyzed oxidative lactonization., HETEROCYCLES, 91(4), pp.782-794; 2015},
 pages = {782--794},
 title = {A Synthesis of Lamellarins via Regioselective Assembly of 1,2,3-Differentially Substituted 5,6-Dihydropyrrolo[2,1-a]Isoquinoline Core},
 volume = {91},
 year = {2015}
}