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- W1481966650 abstract "We report the enantioselective synthesis of the ambergris odorants (+)-(S)-γ-ionone, (+)-(S)-γ-dihydroionone, (−)-α-ambrinol, (+)-(S)-γ-coronal, (−)-(S)-γ-homocyclogeranyl chloride and (+)-(S)-γ-homocyclogeraniol. At first, the enantio-enriched (4R,6S)-4-acetoxy-γ-ionone was prepared starting from commercial racemic ionone alpha by means of a chemo-enzymatic process. This chiral building block was then converted into (S)-γ-dihydroionone which was used as the starting material for the synthesis of the aforementioned odorants. Copyright © 2012 John Wiley & Sons, Ltd." @default.
- W1481966650 created "2016-06-24" @default.
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- W1481966650 date "2012-11-21" @default.
- W1481966650 modified "2023-09-25" @default.
- W1481966650 title "An expedient preparation of enantio-enriched ambergris odorants starting from commercial ionone alpha" @default.
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- W1481966650 doi "https://doi.org/10.1002/ffj.3126" @default.
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