113666-60-7Relevant articles and documents
Sugar-modified foldamers as conformationally defined and biologically distinct glycopeptide mimics
Siriwardena, Aloysius,Pulukuri, Kiran Kumar,Kandiyal, Pancham S.,Roy, Saumya,Bande, Omprakash,Ghosh, Subhash,Garcia Fernandez, Jose Manuel,Ariel Martin, Fernando,Ghigo, Jean-Marc,Beloin, Christophe,Ito, Keigo,Woods, Robert J.,Ampapathi, Ravi Sankar,Chakraborty, Tushar Kanti
supporting information, p. 10221 - 10226 (2013/10/21)
To fold or not to fold? It is shown that attached sugars play a defining role in the conformations adopted by a pair of novel SAA-derived foldamers in water and that these differences are reflected in the contrasting interactions of these glycofoldamers with various biological targets. C green, O red, N blue, H gray; yellow oval=mannose. Copyright
Chemistry of L-Ascorbic and D-Isoascorbic Acids. An Efficient Synthesis of 2-Deoxypentofuranoses
Vargeese, Chandra,Abushanab, Elie
, p. 4400 - 4403 (2007/10/02)
L-Ascorbic and D-isoascorbic acids have been converted to methyl 3-O-benzyl-2-deoxypentofuranosides.The synthetic routes are enantiospecific, efficient, and economic and proceed in high yields.