ol062887v_si_002.cdx (10.89 kB)
Preliminary Studies on the Transformation of Nitrosugars into Branched Chain Iminosugars: Synthesis of 1,4-Dideoxy-4-C-hydroxymethyl- 1,4-imino-pentanols
datasetposted on 15.02.2007, 00:00 by José M. Otero, Raquel G. Soengas, Juan C. Estévez, Ramón J. Estévez, David J. Watkin, Emma L. Evinson, Robert J. Nash, George W. J. Fleet
A novel promising strategy for the transformation of nitrosugars into branched pyrrolidines, based on double Henry reaction with formaldehyde followed by reductive ring closure, allowed the first enantiospecific synthesis of a 4-C-hydroxymethyl branched derivative of the well-known glycosidase inhibitor 1,4-dideoxy-1,4-imino-pentanol. This strategy also afforded a new route to some other interesting derivatives, such as N-hydroxy, N-propyloxy, and imino derivatives, a new kind of compounds with promising biological properties.