Literature DB >> 10552570

Synthesis of deuterated volatile lipid degradation products to be used as internal standards in isotope dilution assays. 1. Aldehydes.

J Lin1, D H Welti, F A Vera, L B Fay, I Blank.   

Abstract

The isotopically labeled compounds [5,6-(2)H(2)]hexanal (d-I), [2, 3-(2)H(2)]-(E)-2-nonenal (d-II), [3,4-(2)H(2)]-(E,E)-2,4-nonadienal (d-III), and [3,4-(2)H(2)]-(E,E)-2,4-decadienal (d-IV) were prepared in good yields using new or improved synthesis procedures. Labeling position, chemical purity, and isotopic distribution of the compounds were characterized by various MS and NMR techniques. These molecules are used as internal standards in quantification experiments based on isotope dilution assay. Synthesis of d-I, d-III, and d-IV has not yet been reported in the literature.

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Year:  1999        PMID: 10552570     DOI: 10.1021/jf9902088

Source DB:  PubMed          Journal:  J Agric Food Chem        ISSN: 0021-8561            Impact factor:   5.279


  3 in total

1.  Quantification of key odorants formed by autoxidation of arachidonic acid using isotope dilution assay.

Authors:  J Lin; L B Fay; D H Welti; I Blank
Journal:  Lipids       Date:  2001-07       Impact factor: 1.880

2.  Synthesis of trans-4,5-epoxy-(E)-2-decenal and its deuterated analog used for the development of a sensitive and selective quantification method based on isotope dilution assay with negative chemical ionization.

Authors:  J Lin; L B Fay; D H Welti; I Blank
Journal:  Lipids       Date:  1999-10       Impact factor: 1.880

3.  Computational design of syntheses leading to compound libraries or isotopically labelled targets.

Authors:  Karol Molga; Piotr Dittwald; Bartosz A Grzybowski
Journal:  Chem Sci       Date:  2019-08-16       Impact factor: 9.825

  3 in total

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