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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

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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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Enzyme-Mediated Preparation of Chiral 1,
✍ Agnese Abate; Elisabetta Brenna; Giovanni Fronza; Claudio Fuganti; Sabrina Ronza 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 German ⚖ 160 KB

## 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