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  Synthesis of new biosynthetically important diarylheptanoids and their oxa- and fluoro-analogues by three different strategies

Baranovsky, A., Schmitt, B., Fowler, D. J., & Schneider, B. (2003). Synthesis of new biosynthetically important diarylheptanoids and their oxa- and fluoro-analogues by three different strategies. Synthetic Communications, 33(6), 1019-1045. doi:10.1081/SCC-120016367.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0012-B5CB-9 Version Permalink: https://hdl.handle.net/21.11116/0000-0009-37E7-5
Genre: Journal Article

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NMR075.pdf (Publisher version), 0B
 
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 Creators:
Baranovsky, A.1, Author           
Schmitt, B.1, Author           
Fowler, D. J.1, Author           
Schneider, B.1, Author           
Affiliations:
1Research Group Biosynthesis / NMR, MPI for Chemical Ecology, Max Planck Society, ou_421898              

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Free keywords: diarylheptanoids; alcol reaction; Wittig reaction; Wittig- horner reaction Biosynthesis
 Abstract: Wittig, aldol and Wittig-Horner reactions have been used to synthesize new diarylheptanoids, which are putative intermediates in phenylphenalenone biosynthesis in plants. The Wittig-Horner approach was most suitable and gave significantly higher yields

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 Dates: 2003
 Publication Status: Issued
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 Rev. Type: -
 Identifiers: Other: NMR075
DOI: 10.1081/SCC-120016367
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Title: Synthetic Communications
  Other : Synth. Commun.
Source Genre: Journal
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Publ. Info: New York : M. Dekker
Pages: - Volume / Issue: 33 (6) Sequence Number: - Start / End Page: 1019 - 1045 Identifier: ISSN: 0039-7911
CoNE: https://pure.mpg.de/cone/journals/resource/954925448758