Exploiting N-(tert-butoxycarbonyl)-2-(tert-butyldimethylsiloxy)pyrrole (TBSOP) as a masked glycine anion equivalent, a short enantiospecific synthesis of the title C-glycosyl α-aminoacid 5 was devised and executed, via diastereospecific α-C-glycosylation of protected arabinose 1 at the anomeric carbon. © 1995.
Diastereoselective synthesis of α-C-arabinofuranosyl glycine / Rassu, G.; Zanardi, F.; Battistini, L.; Casiraghi, G.. - In: TETRAHEDRON-ASYMMETRY. - ISSN 0957-4166. - 6:2(1995), pp. 371-374. [10.1016/0957-4166(95)00016-I]
Diastereoselective synthesis of α-C-arabinofuranosyl glycine
Zanardi F.;Battistini L.;Casiraghi G.
1995-01-01
Abstract
Exploiting N-(tert-butoxycarbonyl)-2-(tert-butyldimethylsiloxy)pyrrole (TBSOP) as a masked glycine anion equivalent, a short enantiospecific synthesis of the title C-glycosyl α-aminoacid 5 was devised and executed, via diastereospecific α-C-glycosylation of protected arabinose 1 at the anomeric carbon. © 1995.File in questo prodotto:
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