Pinkerton, DavidBanwell, MartinWillis, Anthony2015-12-101523-7060http://hdl.handle.net/1885/38817The acetate salts of tambjamines C, E, and F (2-4, respectively), as well as those of the related alkaloids BE-18591 (5) and 6, have been prepared by treatment of bipyrrole aldehyde 16 with the relevant amine in the presence of acetic acid. The 5′-bromcKeywords: alkaloid; BE 18591; pyrrole derivative; unclassified drug; article; chemical structure; chemistry; Pseudoalteromonas; stereoisomerism; synthesis; X ray crystallography; Alkaloids; Crystallography, X-Ray; Models, Molecular; Molecular Structure; PseudoalterTotal syntheses of tambjamines C, E, F, G, H, I and J, BE-18591 and a related alkaloid from the marine bacterium Pseudoalteromonas tunicata200710.1021/ol70243132015-12-09