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Convenient and efficient syntheses of 4-hydroxy-2(E)-nonenal and 4-oxo-2(E)-nonenal

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dc.contributor.author Kurangi, R.F.
dc.contributor.author Tilve, S.G.
dc.contributor.author Blair, I.A.
dc.date.accessioned 2015-06-03T09:00:03Z
dc.date.available 2015-06-03T09:00:03Z
dc.date.issued 2006
dc.identifier.citation Lipids. 41(9); 2006; 877-880. en_US
dc.identifier.uri http://dx.doi.org/10.1007/s11745-006-5043-4
dc.identifier.uri http://irgu.unigoa.ac.in/drs/handle/unigoa/1848
dc.description.abstract Lipid peroxidation products 4-hydroxy-2(E)-nonenal (HNE) and 4-oxo-2(E)-nonenal (ONE) were conveniently synthesized using Wittig and Horner-Wardsworth-Emmons (HWE) reaction. Wittig or HWE reaction between an easily prepared phosphorane or phosphonate with glyoxal dimethyl acetal gave a protected 4-oxo-2(E)-nonenal. Hydrolysis gave 4-oxo-2(E)-nonenal, whereas reduction followed by hydrolysis gave 4-hydroxy-2(E)-nonenal. en_US
dc.publisher Springer Verlag (Germany) en_US
dc.subject Chemistry en_US
dc.title Convenient and efficient syntheses of 4-hydroxy-2(E)-nonenal and 4-oxo-2(E)-nonenal en_US
dc.type Journal article en_US
dc.identifier.impf y


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