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  The first synthesis of geranyllinalool enantiomers

Svatos, A., Urbanova, K., & Valterova, I. (2002). The first synthesis of geranyllinalool enantiomers. Collection of Czechoslovak Chemical Communications, 67(1), 83-90. doi:10.1135/cccc20020083.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0012-B3C3-5 Version Permalink: https://hdl.handle.net/21.11116/0000-0009-380C-C
Genre: Journal Article

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MS024.pdf (Publisher version), 0B
 
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Svatos, A.1, Author           
Urbanova, K., Author
Valterova, I., Author
Affiliations:
1Research Group Mass Spectrometry, MPI for Chemical Ecology, Max Planck Society, ou_421899              

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Free keywords: terpenoids; diterpenes; alcohols; absolute configuration; marking pheromones; bumblebees; cuprates; cross-coupling reactions; carbometallation Labial gland secretion; bumblebees; component; males
 Abstract: (3R)-(-)-Geranyllinalool and its (3S)-(+)-isomer were synthesized in 7 steps starting from both enantiomers of citramalic acid and geranyl bromide. The synthetic sequence established the absolute configurations of naturally occurring geranyllinalools fo

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 Dates: 2002
 Publication Status: Issued
 Pages: -
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 Rev. Type: -
 Identifiers: Other: MS024
DOI: 10.1135/cccc20020083
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Title: Collection of Czechoslovak Chemical Communications
  Other : Collect. Czech. Chem. Commun.
Source Genre: Journal
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Publ. Info: Prague : Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic [etc.]
Pages: - Volume / Issue: 67 (1) Sequence Number: - Start / End Page: 83 - 90 Identifier: ISSN: 0010-0765
CoNE: https://pure.mpg.de/cone/journals/resource/954925391300