Biosynthetic insights provided by unusual sesterterpenes from the medicinal herb Aletris farinosa
Author:
Affiliation:
1. School of Chemistry and Molecular Biosciences
2. The University of Queensland
3. Brisbane 4072
4. Australia
5. Integria Healthcare Pty. Ltd.
6. Brisbane 4133
Abstract
Configuration of a single stereocenter determines if a key carbocation in sesterterpene biosynthesis undergoes simple elimination or a cascade of seven 1,2-methyl and hydride migrations.
Funder
Australian Research Council
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2015/SC/C5SC02056E
Reference27 articles.
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3. Cyclization of All-E- and 2Z-Geranylfarnesols by a Bacterial Triterpene Synthase: Insight into Sesterterpene Biosynthesis inAleuritopterisFerns
4. Terpenoid synthase structures: a so far incomplete view of complex catalysis
5. J. MacMillan and M. H.Beale , in Comprehensive Natural Products Chemistry , ed. D. E. Cane , Elsevier Science , Oxford , 1999 , vol. 2 , ch. 2.08, pp. 217–243
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