Synthesis of novel cationic cardiolipin analogues for the optimal delivery of therapeutic agents

Article abstract of DOI:10.1016/j.tetlet.2004.02.044

A novel approach was developed to synthesize cardiolipin analogues containing two quaternary ammonium groups with tetraalkyl chain retaining 'glycerol' moiety, the central core of the molecule. The analogues were synthesized with or without spacer and/or