Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/106799
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Type: Journal article
Title: Biosynthetically-inspired oxidations of capillobenzopyranol
Author: Pepper, H.
Lam, H.
George, J.
Citation: Organic and Biomolecular Chemistry, 2017; 15(22):4811-4815
Publisher: Royal Society of Chemistry
Issue Date: 2017
ISSN: 1477-0520
1477-0539
Statement of
Responsibility: 
Henry P. Pepper, Hiu C. Lam and Jonathan H. George
Abstract: The synthesis of verrubenzospirolactone from its proposed biosynthetic precursor, capillobenzopyranol, has been shown to be chemically feasible via a simple reaction sequence. The key steps are a chemoselective furan oxidation mediated by NaClO₂, a stereoselective dehydration of a γ-methoxybutenolide, and an intramolecular Diels-Alder reaction.
Rights: This journal is © The Royal Society of Chemistry 2017
DOI: 10.1039/c7ob00868f
Grant ID: http://purl.org/au-research/grants/arc/DP160103393
Published version: http://dx.doi.org/10.1039/c7ob00868f
Appears in Collections:Aurora harvest 8
Chemistry publications

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