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  Biosynthesis of anthecotuloide, an irregular sesquiterpene lactone from Anthemis cotula L. (Asteraceae) via a non-farnesyl diphosphate route

Van Klinik, J., Becker, H., Andersson, S., & Boland, W. (2003). Biosynthesis of anthecotuloide, an irregular sesquiterpene lactone from Anthemis cotula L. (Asteraceae) via a non-farnesyl diphosphate route. Organic and Biomolecular Chemistry, 1(9), 1503-1508. doi:10.1039/b300877k.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0012-A416-4 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0012-A418-F
Genre: Journal Article

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Van Klinik, J., Author
Becker, H., Author
Andersson, S.1, Author           
Boland, W.1, Author           
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1Department of Bioorganic Chemistry, MPI for Chemical Ecology, Max Planck Society, ou_24028              

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Free keywords: Chamomile sesquiterpenes; isoprenoid biosynthesis; terpenoid biosynthesis; higher-plants; pathway; protein; units; c-13
 Abstract: Retrobiosynthetic analysis of the allergenic sesquiterpene lactone, anthecotuloide, suggested that this natural product could be formed either by head to head condensation of geranyl diphosphate with dimethylallyl diphosphate, or from farnesyl diphospha

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 Dates: 2003
 Publication Status: Issued
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 Identifiers: DOI: 10.1039/b300877k
Other: BOL097
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Title: Organic and Biomolecular Chemistry
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Source Genre: Journal
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Pages: - Volume / Issue: 1 (9) Sequence Number: - Start / End Page: 1503 - 1508 Identifier: -