Unsaturated epoxy hydroxy acid

Scheme 17 Generation of unsaturated epoxy hydroxy acids by non enzymic induced oxidation of linoleic acid...

Introduction Primary Fatty Acids Fatty Acids of Plant Vegetative Parts Biosynthesis Fatty Acid Biosynthesis The Two-Pathway Model of Lipid Biosynthesis The Second 3-Ketoacyl ACP Synthase Isozyme Biosynthesis of Unsaturated Fatty Acids The Prokaryotic Pathway The Eukaryotic Pathway Biosynthesis of Triacylglycerides Degradation of Fatty Acids Unusual Fatty Acids in Plants Fatty Acids from Unusual Starter Units Fatty Acids with Unusual Patterns of Unsaturation Hydroxy Fatty Acids Epoxy Fatty Acids... 

Silver ion TLC has also been used for separation of a variety of substituted unsaturated fatty acids such as epoxy, hydroxy and halohydroxy fatty acids, and these have been reviewed by Morris and Nichols (1972). Wax esters and steryl esters exhibit similar polarities and do not separate on column chromatography or normal silica TLC. Kiosseoglou and Boskou (1990) have separated the wax esters from steryl esters by using argentation TLC. They have used silica gel plates impregnated with 10% silver nitrate, with developing solvent hexane/chloroform (7 3 vol./vol.). 

The presence of 5,8,12-trihydroxyoctadeca-rra 5 -9-enoic acid in wheat bran has been demonstrated. Three hitherto unknown oxygenated acids [(5)—(7)] have been found in Stenachaenium macrocephalum after storage for 2 years at 5 °C. These are probably derived from the uncommon octadeca-trienoic acid (3t9cl2c) present in this seed oil, and these results are reminiscent of the isolation of unsaturated epoxy- and hydroxy-acids from sunflower seed oil after prolonged storage. ... 

An interesting new method for the conversion of [I, y-epoxy sulfones (82) to cyclo-alkenones (85) has been developed61. It includes the addition of alkyllithium to y-hydroxy-a,/ -unsaturated sulfones generated from 82 and the alkylation of sulfonyl carbanion thus formed. Oxidation of the resulting y-hydroxy sulfone to 84 followed by elimination of benzenesulfinic acid gives the desired product 85 in good yields (equation 72)61. 

Reaction of the carbanion of chloromethyl phenyl sulphoxide 409 with carbonyl compounds yields the corresponding 0-hydroxy adducts 410 in 68-79% yield. Each of these compounds appears to be a single isomer (equation 242). Treatment of adducts 410 with dilute potassium hydroxide in methanol at room temperature gives the epoxy sulphoxides 411 (equation 243). The ease of this intramolecular displacement of chloride ion contrasts with a great difficulty in displacing chloride ion from chloromethyl phenyl sulphoxide by external nucleophiles . When chloromethyl methyl sulphoxide 412 is reacted with unsymmetrical ketones in the presence of potassium tcrt-butoxide in tert-butanol oxiranes are directly formed as a mixture of diastereoisomers (equation 244). a-Sulphinyl epoxides 413 rearrange to a-sulphinyl aldehydes 414 or ketones, which can be transformed by elimination of sulphenic acid into a, 8-unsaturated aldehydes or ketones (equation 245). The lithium salts (410a) of a-chloro-/ -hydroxyalkyl... 

Hayakawa and Shimizu developed a novel C-C bond-forming reaction by epoxi-dation of methoxyallene 145 with m-chloroperbenzoic acid, which provides a meth-oxyallene oxide intermediate capable of adding to aldehydes. This reaction sequence provides 3-hydroxy-2-methoxy ketones 234 (Scheme 8.59) [133]. The best anti/syn selectivity was obtained by application of a 1 1 mixture of Til4 and Ti(OiPr)4. They also observed the formation of a,/3-unsaturated ketones 236 under comparable reaction conditions when 1-silylated methoxyallene 235 was employed as starting material (Scheme 8.60) [134]. 

Hydroxyketones are versatile intermediates in the synthesis of pharmaceutical intermediates and heterocyclic molecules. a-Aryl hydroxyketones have been prepared by reaction of aryl aldehydes with 1,4-dioxane followed by reduction with lithium aluminum hydride (LAH) and by the selective LAH reduction of a-silyloxy a,P-unsaturated esters." WissneC has shown that treatment of acid chlorides with tris(trimethylsilyloxy)ethylene affords alkyl and aryl hydroxymethyl ketones. 1-Hydroxy-3-phenyl-2-propanone (3) has been generated by the osmium-catalyzed oxidation of phenylpropene and by the palladium-catalyzed rearrangement of phenyl epoxy alcohoP both in 62% yield. 

Fatty acids with trans or non-methylene-interrupted unsaturation occur naturally or are formed during processing for example, vaccenic acid (18 1 Hr) and the conjugated linoleic acid (CLA) rumenic acid (18 2 9tllc) are found in dairy fats. Hydroxy, epoxy, cyclopropane, cyclopropene acetylenic, and methyl branched fatty acids are known, but only ricinoleic acid (12(/f)-hydroxy-9Z-octadecenoic acid) (2) from castor oil is used for oleochemical production. OUs containing vernolic acid (12(5),13(/ )-epoxy-9Z-octadecenoic acid) (3) have potential for industrial use. 

Acrylates Acrylonitriles Allyl Esters Cellulose esters Epoxies Ethylenic (unsaturated) hydrocarbons Poly-hydroxy esters(eg Pentaerythritol tetramethacrylate,Ethylene Glycol diacrylate) Polyolefins Vinyl compound esters, acids)... 

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