Enantioselective synthesis of tri-deuterated (–)-geosmin to be used as internal standard in quantitation assays

Caterina Porcelli, Johanna Kreissl, Martin Steinhaus*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

For the accurate and sensitive quantitation of the off-flavor compound geosmin, particularly in complex matrices, a stable isotopologue as internal standard is highly advantageous. In this work, we present a versatile synthetic strategy leading from (4aR)-1,4a-dimethyl-4,4a,5,6,7,8-hexahydronaphthalen-2(3H)-one to tri-deuterated (–)-geosmin ((4S,4aS,8aR)-4,8a-dimethyl(3,3,4-2H3)octahydronaphthalen-4a(2H)-ol). The starting material was readily accessible from inexpensive 2-methylcyclohexan-1-one using previously published procedures.

Original languageEnglish
Pages (from-to)476-481
Number of pages6
JournalJournal of Labelled Compounds and Radiopharmaceuticals
Volume63
Issue number11
DOIs
StatePublished - 1 Sep 2020

Keywords

  • (4S,4aS,8aR)-4,8a-dimethyl(3,3,4-H)octahydronaphthalen-4a(2H)-ol
  • (4S,4aS,8aR)-4,8a-dimethyloctahydronaphthalen-4a(2H)-ol
  • (–)-(H)geosmin
  • (–)-geosmin
  • deuteration
  • internal standard
  • musty and earthy off-flavor

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