1979
DOI: 10.1002/ange.19790910706
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Synthese und Biosynthese von Alkoxylipiden

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Cited by 17 publications
(5 citation statements)
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References 208 publications
(7 reference statements)
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“…The synthesis of glycerol ethers was earlier studied in order to modify the hydrophilic (glycerol, diglycerol, triglycerol) and hydrophobic parts (branched or linear chains), allowing the possibility to develop a large class of compounds with useful biological and physical properties . Several studies have demonstrated their original surfactant properties compared to classical nonionic surfactants such as polyethylene glycols (PEGs) synthesized from petrochemicals. For example, Aubry recently defined hydrotropic properties for some short alkylated chain glycerol monoethers (GMEs) .…”
Section: Introduction: Properties and Potential Applications Of Glyce...mentioning
confidence: 99%
“…The synthesis of glycerol ethers was earlier studied in order to modify the hydrophilic (glycerol, diglycerol, triglycerol) and hydrophobic parts (branched or linear chains), allowing the possibility to develop a large class of compounds with useful biological and physical properties . Several studies have demonstrated their original surfactant properties compared to classical nonionic surfactants such as polyethylene glycols (PEGs) synthesized from petrochemicals. For example, Aubry recently defined hydrotropic properties for some short alkylated chain glycerol monoethers (GMEs) .…”
Section: Introduction: Properties and Potential Applications Of Glyce...mentioning
confidence: 99%
“…Thus, it should be of great value to develop a simple and more sustainable method for the reduction of esters and especially triglycerides to give the respective ethers in good yields and avoiding the overreduction to alcohol. [11] Sakai applied the InBr 3 -catalyzed reduction using Et 3 SiH as reducing agent to methyl oleate 1 and methyl 10-undecenoate to give the ethers in 56 % and 72 % yield, respectively. [1b] It is remarkable that the C=C double bond, and especially the cisconfigured double bond of methyl oleate is retained.…”
Section: Introductionmentioning
confidence: 99%
“…Amongthese, glycerol represents one of the major worldwide drop-in chemicals. [9][10][11] As am atter of fact, the preparation of MAGEs through direct glycerole therification has been investigated by using both heterogeneous and homogeneous catalysts. [8] MAGEsa re high-value compounds with severali ndustrial applications in the field of cosmetics,p harmaceuticals, solvents, andd etergents.…”
Section: Introductionmentioning
confidence: 99%
“…[8] MAGEsa re high-value compounds with severali ndustrial applications in the field of cosmetics,p harmaceuticals, solvents, andd etergents. [9][10][11] As am atter of fact, the preparation of MAGEs through direct glycerole therification has been investigated by using both heterogeneous and homogeneous catalysts. [12,13] Glycidol was also recently recognizeda sa ni nteresting and valuable starting chemicalt op roduce MAGEs.…”
Section: Introductionmentioning
confidence: 99%