## 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 stereoi
Enzyme-mediated synthesis of new 1,3-dioxane odorants related to Floropal®
✍ Scribed by Agnese Abate; Elisabetta Brenna; Claudio Fuganti; Stefano Serra
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 176 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0882-5734
- DOI
- 10.1002/ffj.1372
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✦ Synopsis
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 elicited odour sensation, still preserving a pleasant character. The substitution of the methyl group at C~6~ with just an ethyl moiety completely changes the odour profile of the molecule. Even subtler are the odour differences generated by configurational variations. Copyright © 2004 John Wiley & Sons, Ltd.
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