The allyl ether as a protecting group in carbohydrate chemistry. Part 10. Synthesis of 3-O-(β-D-galactopyranosyl 3-sulphate)-2-O-hexadecanoyl-1-O-hexadecyl-L-glycerol, ‘seminolipid’
- 1 January 1979
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 3,p. 712-718
- https://doi.org/10.1039/p19790000712
Abstract
3-O-Allyl-L-glycerol was converted, by way of the 1-O-trityl derivative, into 3-O-allyl-2-O-(but-2-enyl)-L-glycerol, which was alkylated with hexadecyl bromide and sodium hydride in NN-dimethylformamide. The product was converted, by the action of potassium t-butoxide in dimethyl sulphoxide, into 1-O-hexadecyl-3-O-(prop-1-enyl)-L-glycerol which was alkylated with ‘crotyl bromide’ and the product was hydrolysed to give 2-O-(but-2-enyl)-1-O-hexadecyl-L-glycerol. This was condensed with acetobromogalactose to give the β-galactoside which was converted into crystalline 2-O-(but-2-enyl)-1-O-hexadecyl-3-O-(3,4-O-isopropylidene-β-D-gaiactopyranosyl)-L-glycerol. This, on benzylation followed by acidic hydrolysis, gave 3-O-(2,6-di-O-benzyl-β-D-galactopyranosyl)-2-O-(but-2-enyl)-1-O-hexadecyl-L-glycerol which was converted, by way of the O-dibutylstannylidene derivative, into 3-O-(3-O-ally) 2,6-di-O-benzyl-β-D-galactopyranosyl)-2-O-(but-2-enyl)-1-O-hexadecyl-L-glycerol. Benzylation of this compound and subsequent treatment with potassium t-butoxide in dimethyl sulphoxide gave 3-O-[2,4,6-tri-O-benzyl-3-O-(prop-1-enyl)-(β-D-galactopyranosyl]-1-O-hexadecyl-L-glycerol which was acylated with hexadecanoyl chloride in pyridine. The prop-1-enyl group was cleaved by the action of mercury(II) chloride to give crystalline 3-O-(2,4,6-tri-O-benzyl-β-D-galactopyranosyl)-2-O-hexadecanoyl-1-O-hexadecyl-L-glycerol. This compound was sulphated with the pyridine–sulphur trioxide complex and the benzyl groups were removed by catalytic hydrogenolysis in glacial acetic acid to give ‘seminolipid’ with properties similar to those reported for the natural material. ‘Desulphato-seminolipid’[3-O-(β-D-galactopyranosyl)-2-O-hexadecanoyl-1-O-hexadecyl-L-glycerol] was also prepared by catalytic hydrogenolysis of 3-O-(2,4,6-tri-O-benzyl-β-D-galactopyranosyl)-2-O-hexadecanoyl-1-O-hexadecyl-L-glycerol.This publication has 9 references indexed in Scilit:
- Glyceroglucolipids of the Human SalivaEuropean Journal of Biochemistry, 1978
- Sulfated glyceroglycolipids in rat brain. Structure sulfation in vivo, and accumulation in whole brain during development.Journal of Biological Chemistry, 1978
- Partial characterization of glyceroglucolipids from human salivaBiochemical and Biophysical Research Communications, 1977
- The biosynthesis of sulphogalactosyldiacylglycerol of rat brain in vitroBiochemical Journal, 1977
- The association of the sulphogalactosylglycerolipid of rat brain with myelinationBiochemical Journal, 1977
- Glycolipids of the Human Gastric Content. Structure of the Sulfated GlyceroglucolipidEuropean Journal of Biochemistry, 1977
- GLYCOLIPID COMPOSITION OF HUMAN TESTIS AT DIFFERENT AGES AND STEREOCHEMICAL CONFIGURATION OF SEMINOLIPID1977
- Synthesis of 3-O-(3,4-di-O-benzyl-α-D-glucopyranosyl01,2-O-isopropylidene-SN-glycerolChemistry and Physics of Lipids, 1976
- A comparative study of the glycolipids of human, bird and fish testes and of human spermBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1976