Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/51291

TitleDiastereoselective synthesis of analogues of neuraminic acid
Author(s)Duarte, Vera C. M.
Fortes, A. Gil
Alves, Maria José Chão
Issue date2015
Abstract(s)Siliac acids frequently terminate oligosaccharide side chains in glycoproteins and glycolipids. In this position they have been found to mask recognition by proteases or glycosidases, extending glycoproteins and glycolipids lifetime and function.1 The interest in the sialic acids chemistry in which neuraminic acid is included has rapidly increased in last years, especially since their involvement in the regulation of a great variety of biological phenomena was recognised.2 In our previous work, we found that combination of D-erythrose 1,3-butadiene with t-butyl 2H-azirine 3-carboxylate through Diels-Alder cycloaddition gave as major product the (R)-configured cycloadduct 1, in 58% yield.3 Analogues of neuraminic acid can be achieved from this adduct in a few steps, following different methods of oxidation of the double bound (Scheme 1). Osmilation of the cycloadduct was found to be totally stereo-selective, the addition occurring by the si face. After benzylidene acetal cleavage under acid hydrolysis was obtained product 2. On the other hand, epoxidation of the cycloadduct followed by nucleophilicic ring-opening will give access to the configuration described in compounds 3, and by aziridination of the epoxide is achieved the L-gluco neuraminic acid configuration.
TypePanel presentation
URIhttp://hdl.handle.net/1822/51291
Peer-Reviewedyes
AccessOpen access
Appears in Collections:CDQuim - Comunicações e Proceedings

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