Cationic ether lipids; containing nitrogenous heterocyclic bases as the positively charged groups were synthesized. Treatment of methylthiomethyl ethers of dialkylglycerols with bromine afforded highly reactive alpha-bromo ethers. These products reacted with various nucleophilic reagents giving rise to a series of cationic alkylglycerols.
Synthesis of new alkyl-type glycerolipids from methylthiomethyl ethers
作者:N. V. Plyavnik、M. A. Maslov、G. A. Serebrennikova
DOI:10.1007/s11172-008-0298-y
日期:2008.10
The synthesis of alkyl-type glycerolipids with aliphatic and heterocyclic cationic “heads” separated by an acetal spacer from the glycerol core is described. The synthesis of sulfur-containing glycerolipids with an ether bond from rac-1-O-(2-bromoethoxy)methyl-2-O-ethyl-3-O-octadecylglycerol and functionalized thiols is considered.