Synthesis of b-glyco-1,2-diacylglycerols is achieved by a versatile and simple procedure based on trichloro-acetimidate methodology and use of peracetate sugar substrates. The chemical strategy was tested through stereoselective preparation of b-galacto- and b-gluco-lipid derivatives capable to trigger immune system response. The synthetic approach is designed to obtain enantiomerically pure regioand stereo-isomers including derivatives containing poly-unsaturated fatty acids.
An efficient and versatile chemical synthesis of bioactive glyco-glycerolipids / E., Manzo; Ciavatta, M. L.; D., Pagano; Fontana, A. - In: TETRAHEDRON LETTERS. - ISSN 0040-4039. - 53:(2012), pp. 879-881. [10.1016/j.tetlet.2011.12.030]
An efficient and versatile chemical synthesis of bioactive glyco-glycerolipids
Fontana A
2012
Abstract
Synthesis of b-glyco-1,2-diacylglycerols is achieved by a versatile and simple procedure based on trichloro-acetimidate methodology and use of peracetate sugar substrates. The chemical strategy was tested through stereoselective preparation of b-galacto- and b-gluco-lipid derivatives capable to trigger immune system response. The synthetic approach is designed to obtain enantiomerically pure regioand stereo-isomers including derivatives containing poly-unsaturated fatty acids.File | Dimensione | Formato | |
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