Please use this identifier to cite or link to this item: http://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
RMID: 1000002459
DOI: 10.1021/acs.orglett.9b03392
Grant ID: http://purl.org/au-research/grants/arc/FT170100437
Appears in Collections:Chemistry publications

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