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Enantioselective Total Synthesis of cis-Trikentrin B

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journal contribution
posted on 17.05.1996, 00:00 by Mase Lee, Izumi Ikeda, Tsuyoshi Kawabe, Sayaka Mori, Ken Kanematsu
Natural cis-trikentrin B was synthesized enantioselectively using, as key steps, an intramolecular Diels−Alder reaction of an allenic dienamide followed by aromatization to construct an indole ring and cleavage of bicyclo[2.2.1]heptene to launch a cis-dimethylcyclopentane ring. Diels−Alder adducts 9 and 10 were elaborated to provide allenic dienamide 25, and its intramolecular Diels−Alder reaction proceeded smoothly. Aromatization to an indole ring and stereoselective cleavage of the bicyclo[2.2.1]heptene ring were performed successfully. Introduction of an (E)-butenyl group via addition of propylmagnesium bromide and subsequent anti elimination of water gave natural cis-trikentrin B.

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