Total Synthesis of Calyciphylline F
Abstract Calyciphylline F represents the final challenge in the total synthesis of the caged polycyclic‐type of Daphniphyllum alkaloids due to the strained 8‐azatricyclo[4.2.1.0 4,8 ]nonane ring system. Here, we report the total synthesis of calyciphylline F. We construct the ring system by applying [4 + 3] cycloaddition reaction of pyrroles with 2‐oxyallyl cations to an intramolecular reaction, followed by an intramolecular aldol reaction and capture of the resulting alkoxide as the xanthate. The bridgehead quaternary carbon center is constructed by the intramolecular addition reaction of the bridgehead radical to the alkoxy‐acrylate, which is designed based on the proposed mechanism of by‐product formation. Finally, another 6‐ exo ‐radical cyclization reaction constructs the last remaining ring and achieves the total synthesis of calyciphylline F.
Authors
- Ryota Kotaka
- Sangita Karanjit (ORCID: https://orcid.org/0000-0003-0151-5893)
- Kosuke Namba (ORCID: https://orcid.org/0000-0003-1548-5656)
- Ryota Sato (ORCID: https://orcid.org/0009-0005-6940-9159)
- Masakí Inoue (ORCID: https://orcid.org/0000-0002-2912-9305)
- Ryuichi Sumida
Institutions
- Toneyama National Hospital (JP)
- Zero to Three (US)
- Tokushima University (JP)
- The University of Osaka (JP)
Publication Details
- Journal
- Angewandte Chemie
- Published
- 2025-09-15
- DOI
- https://doi.org/10.1002/ange.202517671
- Primary Topic
- Advanced Synthetic Organic Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- University of Tokushima
- Japan Society for the Promotion of Science