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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 language | English |
|---|---|
| Pages (from-to) | 476-481 |
| Number of pages | 6 |
| Journal | Journal of Labelled Compounds and Radiopharmaceuticals |
| Volume | 63 |
| Issue number | 11 |
| DOIs | |
| State | Published - 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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Dive into the research topics of 'Enantioselective synthesis of tri-deuterated (–)-geosmin to be used as internal standard in quantitation assays'. Together they form a unique fingerprint.Activities
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Interne Dissertationsprüfung von Caterina Porcelli
Steinhaus, M. (Examiner) & Schwab, W. (Examiner)
26 Jul 2022Activity: Examiner