Issue 2, 2020

Synthesis of natural 1-O-alkylglycerols: a study on the chemoselective opening of the epoxide ring by onium quaternary salts (N and P) and ionic liquids

Abstract

A chemoselective route for the synthesis of 1-O-alkylglycerols chimyl (1), batyl (2), and selachyl (3) is reported. These compounds can be naturally isolated from shark liver oil and the skin of animals such as stingrays and chimeras and exhibit potential anti-fouling activity. The synthetic approach developed in this work included two distinct methods of preparation. The first was based on solvent-free reactions catalyzed by onium quaternary salts (N and P) and ionic liquids; the second methodology was based on a series of one-pot reactions.

Graphical abstract: Synthesis of natural 1-O-alkylglycerols: a study on the chemoselective opening of the epoxide ring by onium quaternary salts (N and P) and ionic liquids

Supplementary files

Article information

Article type
Paper
Submitted
06 Nov 2019
Accepted
16 Dec 2019
First published
03 Jan 2020
This article is Open Access
Creative Commons BY license

RSC Adv., 2020,10, 1050-1054

Synthesis of natural 1-O-alkylglycerols: a study on the chemoselective opening of the epoxide ring by onium quaternary salts (N and P) and ionic liquids

T. S. Nascimento, E. F. Braga, G. C. Casaes Gomes, W. R. Batista, A. L. Mazzei Albert, R. S. Capella Lopes and C. C. Lopes, RSC Adv., 2020, 10, 1050 DOI: 10.1039/C9RA09217J

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