Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/115905
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Type: Journal article
Title: Biomimetic synthesis of hyperjapones F-I
Author: Lam, H.
Phan, Q.
Sumby, C.
George, J.
Citation: Australian Journal of Chemistry, 2018; 71(9):649-654
Publisher: CSIRO Publishing
Issue Date: 2018
ISSN: 0004-9425
1445-0038
Statement of
Responsibility: 
Hiu C. Lam, Quang D. Phan, Christopher J. Sumby, and Jonathan H. George
Abstract: Hyperjapones F–I are tetracyclic meroterpenoids recently isolated from Hypericum japonicum. All four of these natural products have been synthesised using oxidative, intermolecular hetero-Diels–Alder reactions to couple their common biosynthetic precursor, norflavesone, to the appropriate monoterpene building blocks: sabinene, β-pinene, and α-pinene. The synthesis of enantiomerically pure hyperjapones H and I and comparison of their optical rotations to those of the natural samples indicated that these meroterpenoids are probably biosynthesised as either racemic or scalemic mixtures.
Description: Published online: 6 July 2018
Rights: Journal compilation © CSIRO 2018
RMID: 0030097230
DOI: 10.1071/CH18141
Grant ID: http://purl.org/au-research/grants/arc/DP160103393
http://purl.org/au-research/grants/arc/FT170100437
Appears in Collections:Chemistry publications

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