Total Synthesis and Anti-inflammatory Activity of Stemoamide-Type Alkaloids Including Totally Substituted Butenolides and Pyrroles

Yasuki Soda, Yasukazu Sugiyama, Shunsei Sato, Kana Shibuya, Junya Saegusa, Tomoe Matagawa, Sayaka Kawano, Makoto Yoritate, Keisuke Fukaya, Daisuke Urabe, Takeshi Oishi, Kento Mori, Siro Simizu, Noritaka Chida, Takaaki Sato

Research output: Contribution to journalArticlepeer-review

Abstract

The totally substituted butenolide including two tetrasubstituted olefins is a distinct structural motif seen in Stemona alkaloids, but efficient methods for its synthesis are not well developed. As an ongoing program aimed at the collective total synthesis of the stemoamide group, we report a stereodivergent method to give either (E)-or (Z)-totally substituted butenolide from the same intermediate. While the AgOTf-mediated elimination via the E1-type mechanism results in the formation of the kinetic (Z)-tetrasubstituted olefin, the subsequent TfOH-mediated isomerization gives the thermodynamic (E)-tetrasubstituted olefin. The pyrrole ring is another important structure found in Stemona alkaloids. The direct oxidation of pyrrolidine rings with MnO2 and careful purification give the pyrrole groups without isomerization of the stereocenter in the lactone group. These two methods enable us to synthesize a series of stemoamide-type alkaloids including tricyclic, tetracyclic and pentacyclic frameworks. The anti-inflammatory activities by inhibition of iNOS expression in macrophage cell line RAW264.7 indicate that the most potent anti-inflammatory compounds without cytotoxicity are protostemonines, which consist of pentacyclic frameworks including the totally substituted butenolide.

Original languageEnglish
JournalSynthesis (Germany)
DOIs
Publication statusAccepted/In press - 2022

Keywords

  • Amide
  • anti-inflammatory
  • butenolide
  • DFT calculation
  • iNOS
  • pyrrole
  • Stemona alkaloids
  • total synthesis

ASJC Scopus subject areas

  • Catalysis
  • Organic Chemistry

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