301329-75-9Relevant academic research and scientific papers
Synthesis and liquid crystalline properties of mono-, di- and tri-O-alkyl pentaerythritol derivatives bearing tri-, di- or monogalactosyl heads: The effects of curvature of molecular packing on mesophase formation
Dumoulin, Fabienne,Lafont, Dominique,Huynh, Thai-Le,Boullanger, Paul,Mackenzie, Grahame,West, Jon J.,Goodby, John W.
, p. 5585 - 5600 (2008/03/12)
Self-organisation and self-assembly are critical to the stability of synthetic and biological membranes. Of particular importance is consideration of the packing arrangements of the various molecular species. Both phosphoand glycolipids can pack in ways in which curvature can be introduced into self-organised or self-assembled systems. For instance, it is known that the degree of curvature can affect the structures of any condensed phases that are formed. In this article we report on a systematic study in which we have varied the shapes of glycolipids and examined the condensed phases that they form. In doing so, we have also unified the shape dependency of lyotropic liquid crystals with those of thermotropic liquid crystals. In order to undertake this systematic study a range of different pentaerythritol derivatives was synthesized, which covers combinations of one to three alkyl chains of different lengths (6,7,9,10,11,12,14,16 carbon atoms) and three to one galactosyl heads. Monoand di-O-galactosyl derivatives were prepared directly by glycosylation of the corresponding alcohols using 2,3,4,6-tetra-O-benzoyl or acetyl-α-D- galactopyranosyl trichloroacetimidate or bromide as the donors; the tri-O-galactosyl derivatives were synthesized from O-alkyl-O-benzyl di-O-galactosyl pentaerythritol intermediates, followed by de-O-benzylation and glycosylation steps. All of the fully deprotected products were obtained by standard methods, and their self-organising and self-assembling properties examined.
Synthesis of polyfunctional pentaerythritol-derivatives using a novel protective group strategy for the preparation of cluster-glycolipids
Schmidt,Dobner,Nuhn
, p. 1157 - 1159 (2007/10/03)
We describe new derivatives of pentaerythritol suitable for the synthesis of polyantennary cluster glycolipids with different headgroups. Key substance is a pentaerythritol with one hydrophobic moiety as lipophilic anchor, an unprotected primary hydroxyl group and two differently protected hydroxyl groups.
