Adelaide Research & Scholarship
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https://hdl.handle.net/2440/122676
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| Type: | Journal article |
| Title: | Biomimetic synthesis enables the structure revision of furoerioaustralasine |
| Author: | Coleman, M.A. Burchill, L. Sumby, C.J. George, J.H. |
| Citation: | Organic Letters, 2019; 21(21):8776-8778 |
| Publisher: | American Chemical Society |
| Issue Date: | 2019 |
| ISSN: | 1523-7060 1523-7052 |
| Statement of Responsibility: | Matthew A. Coleman, Laura Burchill, Christopher J. Sumby, and Jonathan H. George |
| Abstract: | The structure of furoerioaustralasine, a unique Australian alkaloid, has been revised based on a concise, biomimetic synthesis. The key step is a stereospecific, intramolecular ring opening of an epoxide to form a central dihydrofuran fused to a quinoline ring system. |
| Keywords: | Alkaloids Biomimetics Cyclization Chemistry Techniques, Synthetic |
| Rights: | © 2019 American Chemical Society |
| DOI: | 10.1021/acs.orglett.9b03392 |
| Grant ID: | http://purl.org/au-research/grants/arc/FT170100437 |
| Published version: | http://dx.doi.org/10.1021/acs.orglett.9b03392 |
| Appears in Collections: | Aurora harvest 4 Chemistry publications |
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