Data di Pubblicazione:
2010
Citazione:
Chemoselective synthesis of sialic acid 1,7-lactones / P. Allevi, P. Rota, R. Scaringi, R. Colombo, M. Anastasia. - In: JOURNAL OF ORGANIC CHEMISTRY. - ISSN 0022-3263. - 75:16(2010), pp. 5542-5548.
Abstract:
The chemoselective synthesis of the 1,7-lactones of N-acetylneuraminic acid, N-glycolylneuraminic acid, and 3-deoxy-D-glycero-D-galacto-nononic acid is accomplished in two steps: a simple treatment of the corresponding free sialic acid with benzyloxycarbonyl chloride and a successive hydrogenolysis of the formed 2-benzyloxycarbonyl 1,7-lactone. The instability of the 1,7-lactones to protic solvents has been also evidenced together with the rationalization of the mechanism of their formation under acylation conditions. The results permit to dispose of authentic 1,7-sialolactones to be used as reference standards and of a procedure useful for the preparation of their isotopologues to be used as inner standards in improved analytical procedures for the gas liquid chromatography-mass spectrometry (GLC-MS) analysis of 1,7-sialolactones in biological media
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
sialic acid ; N-acetylneuraminic acid 1,7-lactone ; N-glycolylneuraminic acid 1,7-lactone ; sialic acid lactones
Elenco autori:
P. Allevi, P. Rota, R. Scaringi, R. Colombo, M. Anastasia
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