4.7 Article

Total synthesis of (+)-cylindradine A

Journal

CHEMICAL COMMUNICATIONS
Volume 50, Issue 53, Pages 6991-6994

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c4cc00137k

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Funding

  1. JSPS [21655060]
  2. Ministry of Education, Culture, Sports, Science and Technology, Japan
  3. Grants-in-Aid for Scientific Research [26282214, 26560444] Funding Source: KAKEN

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Cylindradines A and B, members of the polycyclic pyrrole-imidazole alkaloids (PIAs), are the only congeners bearing a 3-carbamoylpyrrole unit among the PIAs. In this communication, we described a total synthesis of (+)-cylindradine A based on intramolecular Friedel-Crafts type cyclization of pyrrole-aldehyde and oxidative cyclization of tricyclic pyrrolopyrrolidine-guanidine with hypervalent iodine to construct the cyclic guanidine structure including the N,N'-aminal moiety.

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