168975-26-6Relevant articles and documents
New synthesis of both D- and L-3-O-carbamoyl-2-deoxy-4-thioribosides, substrates for β-selective glycosylations
Shaw-Ponter, Sue,Rider, Peter,Young, Robert J.
, p. 1871 - 1874 (2007/10/03)
A new route to intermediates for the synthesis of 2'-deoxy-4'-thionucleosides is described. By utilising enantiomeric erythro-dibenzyldithioacetals, both D- and L-3-O-(N-acyl)carbamoyl thiosugars, which give β-selective glycosylations, are readily produced.