| Literature DB >> 28488778 |
Keisuke Nishikawa1, Kengo Yamauchi1, Seiho Kikuchi1, Shinnosuke Ezaki1, Tomoyuki Koyama1, Haruka Nokubo1, Kunihiro Matsumura1, Takeshi Kodama1, Momochika Kumagai1,2, Yoshiki Morimoto1.
Abstract
The enantioselective total syntheses of lepadiformine marine alkaloids, azatricyclic natural products isolated from marine tunicates, were completed. These alkaloids have a unique chemical structure characterized by the trans-1-azadecalin (AB ring system) fused with the spirocyclic ring (AC ring system). Here we found that a cycloisomerization reaction from functionalized linear substrates to a 1-azaspiro[4.5]decane framework corresponding to the AC ring in lepadiformines is promoted by a catalytic amount of mercury(II) triflate (Hg(OTf)2 ). The total syntheses of (-)-lepadiformines A and B were achieved in 28 % and 21 % overall yields, respectively, through the novel cycloisomerization reaction. The syntheses of (+)- and (-)-lepadiformine C hydrochloride salts also enabled us to determine the absolute configuration of natural lepadiformine C. It has been found that a phenomenon of enantiodivergence occurs in lepadiformine alkaloids from a single species of marine tunicate, Clavelina moluccensis. The cytotoxic activities of synthesized lepadiformine hydrochloride salts and their synthetic intermediates were evaluated.Entities:
Keywords: alkaloids; cytotoxicity; natural products; spiro compound; total synthesis
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Year: 2017 PMID: 28488778 DOI: 10.1002/chem.201701475
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236