233681-07-7Relevant academic research and scientific papers
A new and convenient approach for the synthesis of rffio- and 2′-deoxyrffio-p-l-furanonucleosides starting from β-l-xylofuranonucleosides
Boudou
, p. 607 - 609 (2007/10/03)
Ribo- and 2′-deoxyribo-β-L-ruranosyladenine have been synthesized. Although these compounds have been already reported in the literature, it seemed to us that a more convenient approach for their synthesis deserved to be developed. Intramolecular substitution as well as Mitsunobu reaction were used to invert the configuration of carbon 3′ of starting β-L-xylofuranosyl intermediates. Copyright
Unnatural β-L-enantiomers of nucleoside analogues as potent anti- hepatitis B virus agents
Gosselin,Boudou,Griffon,Pavia,Pierra,Imbach,Faraj,Sommadossi
, p. 1731 - 1738 (2007/10/03)
Several 2'- or 3'- substituted 2',3'-dideoxy-β-L-nucleosides bearing adenine as the base were stereospecifically synthesized and their antiviral properties examined. Two of them, namely 2'-azido- and 3'-azido-2',3'- dideoxy-β-L-adenosine (2'-N3
