Literature DB >> 15537321

Synthesis of deuterated gamma-lactones for use in stable isotope dilution assays.

Jo-Anna Hislop1, Martin B Hunt, Simon Fielder, Daryl D Rowan.   

Abstract

Two syntheses of deuterated gamma-lactones for use as internal standards in stable isotope dilution assays (SIDA) were developed. [2,2,3,3-2H4]-gamma-Octa-, -gamma-deca-, and -gamma-dodecalactones with >89% deuterium incorporation were prepared in 27, 17, and 19% overall yields, respectively, by the reduction of a doubly protected hydroxypropiolic acid with deuterium gas. [3,3,4-2H3]-gamma-Octa- and -gamma-dodecalactones were prepared in 6 and 23% yields with >92% deuterium incorporation by the free radical addition of 2-iodoacetamide to [1,1,2-2H3]-1-hexene and [1,1,2-2H3]-1-decene, respectively. Reaction yields were highly dependent upon the purity of the 1-alkene starting material. The deuterated gamma-lactones were evaluated as internal standards for SIDA.

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Year:  2004        PMID: 15537321     DOI: 10.1021/jf048885b

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


  1 in total

1.  New biotransformation process for production of the fragrant compound γ-dodecalactone from 10-hydroxystearate by permeabilized Waltomyces lipofer cells.

Authors:  Jung-Ung An; Young-Chul Joo; Deok-Kun Oh
Journal:  Appl Environ Microbiol       Date:  2013-02-08       Impact factor: 4.792

  1 in total

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