Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractAllelochemicals of the phenoxazinone class act at physiologically relevant concentrations    Next AbstractNo Butts on the Beach: Aquatic Toxicity of Cigarette Butt Leachate Chemicals »

Mol Divers


Title:"Microwave-assisted enzymatic synthesis of geraniol esters in solvent-free systems: optimization of the reaction parameters, purification and characterization of the products, and biocatalyst reuse"
Author(s):Venturi V; Presini F; Trapella C; Bortolini O; Giovannini PP; Lerin LA;
Address:"Department of Environment and Prevention Sciences, University of Ferrara - UNIFE, Via Luigi Borsari, 46, Ferrara, 44121, Italy. Department of Chemical, Pharmaceutical and Agricultural Sciences, University of Ferrara - UNIFE, Via Luigi Borsari, 46, Ferrara, 44121, Italy. Department of Chemical, Pharmaceutical and Agricultural Sciences, University of Ferrara - UNIFE, Via Luigi Borsari, 46, Ferrara, 44121, Italy. lrnldm@unife.it"
Journal Title:Mol Divers
Year:2023
Volume:20230627
Issue:
Page Number: -
DOI: 10.1007/s11030-023-10682-y
ISSN/ISBN:1573-501X (Electronic) 1381-1991 (Linking)
Abstract:"Various geraniol esters act as insect pheromones and display pharmacological activities, especially as neuroprotective agents. Therefore, the search for synthetic strategies alternative to traditional chemical synthesis could help designing ecofriendly routes for the preparation of such bioactive compounds. Hence, this work aims at the microwave-assisted enzymatic synthesis of geranyl esters in solvent-free systems. The process variables were optimized for the synthesis of geranyl acetoacetate, achieving 85% conversion after 60 min using a 1:5 substrates molar ratio (ester to geraniol), 80 degrees C and 8.4% of Lipozyme 435 lipase without removal of the co-produced methanol. On the other hand, a 95% conversion was reached after 30 min using 1:6 substrates molar ratio, 70 degrees C and 7% lipase in the presence of 5A molecular sieves for the methanol capture. In addition, the lipase showed good reusability, maintaining the same activity for five reaction cycles. Finally, under the above optimized conditions, other geraniol esters were successfully synthetized such as the geranyl butyrate (98%), geranyl hexanoate (99%), geranyl octanoate (98%), and geranyl (R)-3-hydroxybutyrate (56%). These results demonstrate the microwave-assisted lipase-catalyzed transesterification in a solvent-free system as an excellent and sustainable catalytic methodology to produce geraniol esters"
Keywords:Geranyl (R)-3-hydroxybutyrate Geranyl acetoacetate Geranyl butyrate Geranyl hexanoate Geranyl octanoate Lipozyme 435;
Notes:"PublisherVenturi, Valentina Presini, Francesco Trapella, Claudio Bortolini, Olga Giovannini, Pier Paolo Lerin, Lindomar Alberto eng Netherlands 2023/06/27 Mol Divers. 2023 Jun 27. doi: 10.1007/s11030-023-10682-y"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 22-11-2024