Total synthesis of (-)-martinellic acid via radical addition-cyclization-elimination reaction |
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Authors: | Shirai Atsushi Miyata Okiko Tohnai Norimitsu Miyata Mikiji Procter David J Sucunza David Naito Takeaki |
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Affiliation: | Kobe Pharmaceutical University, Motoyamakita, Higashinada, Kobe, Japan. |
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Abstract: | The asymmetric total synthesis of martinellic acid, the first pyrrolo[3,2-c]quinoline alkaloid found in nature, is described. Three key steps in our synthesis of (-)-martinellic acid are the Bu(3)SnH-promoted radical addition-cyclization-elimination (RACE) reaction of an oxime ether with an alpha,beta-unsaturated ester to generate the pyrrolo[3,2-c]quinoline core, a chemoselective lactam carbonyl reduction, and guanidinylation under Mitsunobu reaction conditions. The key radical cyclization has also been investigated by using SmI(2). (-)-Martinellic acid was synthesized from commercially available methyl 4-bromo-3-methylbenzoate in fewer steps than previous syntheses and in an improved overall yield. |
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