## Abstract The enzyme‐mediated synthesis of enantiomerically enriched 1,3‐dioxane odorants analogous to Floropal^®^ is here described. The complete olfactory evaluation of each sample is also reported. The addition of a single methyl group at C~5~ of the dioxane ring of Floropal^®^ modifies the eli
Enzyme-Mediated Preparation of Chiral 1,3-Dioxane Odorants
✍ Scribed by Agnese Abate; Elisabetta Brenna; Giovanni Fronza; Claudio Fuganti; Sabrina Ronzani; Stefano Serra
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- German
- Weight
- 160 KB
- Volume
- 86
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The enantiomerically enriched diastereoisomers of the chiral 1,3‐dioxane odorants Floropal^®^ (1) and Magnolan^®^ (2) were prepared by an enzyme‐mediated approach. Their olfactory properties were evaluated to investigate differences in the odor perception for the stereoisomers.
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