Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/105562
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Type: Journal article
Title: A biomimetic synthetic approach to the frondosins
Author: Kuan, K.
Hirschvogel, A.
George, J.
Citation: Australian Journal of Chemistry: an international journal for chemical science, 2016; 69(12):1420-1423
Publisher: CSIRO Publishing
Issue Date: 2016
ISSN: 0004-9425
1445-0038
Statement of
Responsibility: 
Kevin K. W. Kuan, Aylin M. C. Hirschvogel and Jonathan H. George
Abstract: The frondosins are a family of five marine sponge-derived meroterpenoids. We propose that the 6-7 ring system common to each of the frondosins is biosynthesized via ring expansion of a 6–6 ring system. Compelling evidence in favour of this proposal was obtained in the form of a biomimetic synthesis of the frondosin 6–7 ring system, which features a highly stereo- and regio-selective ring expansion cascade reaction as the key step.
Rights: Journal compilation © CSIRO 2016
DOI: 10.1071/CH16218
Grant ID: http://purl.org/au-research/grants/arc/DP160103393
Appears in Collections:Aurora harvest 3
Chemistry publications

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