Chemistry of Natural Compounds

, Volume 2, Issue 6, pp 299–302 | Cite as

Investigations in the field of lipids

XLIII. Synthesis of neutral plasmalogens
  • E. A. Parfenov
  • G. A. Serebrennikova
  • S. Ya. Roitberg
  • N. A. Preobrazhenskii
Article

Summary

1. The synthesis of the following neutral plasmalogens has been effected: α-O-(octadec-1-enyl)-β, α′distearoylglycerol, α-O-(octadec-1-enyl)-β, α′-dipalmitoylglycerol, α-O-(hexadec-1-enyl)-β, α′-distearoylglycerol, and α-O-(pentadec-1-enyl)-β, α′-dipalmitoylglycerol.

2. During the synthesis, the following compounds were isolated and characterized by their physicochemical constants: the α-octadec-1-enyl ether of glycerol, α-(2-hydroxyoctadecyl) β, α′-isopropylideneglyceryl ether, the tosylate of α-(2-hydroxyoctadecyl) β, α′-isopropylideneglyceryl ether, and α-O-(2-tosyloxyoctadecyl) glycerol.

3. The IR spectra of the α-octadec-1-enyl ether of glycerol and the neutral plasmalogens have been studied.

Keywords

Vinyl Ether Tosylate Activity Grade Glyceryl Ether Pyridine Hydrochloride 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    O. W. Thiele, Z. klin. Chem.,2, 33, 1964.Google Scholar
  2. 2.
    E. A. Parfenov, G. A. Serebrennikova, and N. A. Preobrazhenskii, ZhOrKh.2, 629, 1966.Google Scholar
  3. 3.
    E. A. Parfenov, G. A. Serebrennikova, and N. A. Preobrazhenskii, ZhOrKh,2, 633, 1966.Google Scholar
  4. 4.
    G. A. Serebrennikova, E. A. Parfenov, N. I. Serebryakova, and N. A. Preobrazhenskii, KhPS, [Chemistry of Natural Compounds], 306, 1966.Google Scholar

Copyright information

© The Faraday Press, Inc. 1968

Authors and Affiliations

  • E. A. Parfenov
    • 1
  • G. A. Serebrennikova
    • 1
  • S. Ya. Roitberg
    • 1
  • N. A. Preobrazhenskii
    • 1
  1. 1.Lomonosov Moscow Institute of Fine Chemical TechnologyUSSR

Personalised recommendations