Abstract
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.
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