Published December 6, 2019
| Supplemental Material
Journal Article
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Progress toward the Enantioselective Synthesis of Curcusones A–D via a Divinylcyclopropane Rearrangement Strategy
Chicago
Abstract
We report our iterative efforts toward the divergent total syntheses of curcusones A–D via Suzuki coupling, intramolecular cyclopropanation, and a key divinylcyclopropane rearrangement. Progress of our synthesis was repeatedly challenged by the highly substrate-dependent cyclopropanation step, which we could ultimately overcome by judicious choice of substituents on the six-membered ring fragment.
Additional Information
© 2019 American Chemical Society. Received: October 27, 2019. Publication Date:November 25, 2019. We thank NSF (CHE-1800511), Amgen, and Caltech for funding this research. Author Contributions: A.C.W. and C.W.L. contributed equally. The authors declare no competing financial interest.Attached Files
Supplemental Material - ol9b03829_si_001.pdf
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Additional details
- Eprint ID
- 100047
- DOI
- 10.1021/acs.orglett.9b03829
- Resolver ID
- CaltechAUTHORS:20191125-151328722
- NSF
- CHE-1800511
- Amgen
- Caltech
- Created
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2019-11-25Created from EPrint's datestamp field
- Updated
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2021-11-16Created from EPrint's last_modified field