176301-76-1Relevant academic research and scientific papers
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.
Acyl carbamate directing groups in nucleoside synthesis: Applications in the synthesis of 2′-deoxy-5-ethyl-4′-thiouridine
Shaw-Ponter, Sue,Mills, Gail,Robertson, Mark,Bostwick, Roy D.,Hardy, George W.,Young, Robert J.
, p. 1867 - 1870 (2007/10/03)
The use of the 3-O-(N-acyl)carbamoyl directing groups in the synthesis of the potent anti-Herpes virus agent 2′-deoxy-5-ethyl-4′-thio-D-uridine is described. This includes details of experiments to optimise the carbamate substitution and a multi-gram exemplification of the key steps.
