118068-35-2Relevant articles and documents
1,3-Dipolar cycloaddition reactions of 3′,5′-Bis-O-silyl thymidines. Synthesis of novel azabicyclic compounds
Negron,Calderon,Vazquez,Lomas,Cardenas,Marquez,Gavino
, p. 1977 - 1984 (2002)
An efficient one step procedure for the preparation of (4.3.0) bicyclic N-methylpyrrolidine thymidine derivatives 4, using cycloaddition reaction of the highly reactive non-stabilized azomethine ylide [Y] with 3′,5′-Bis-O-silylthymidines 3.
Facile preparation of protected furanoid glycals from thymidine
Cameron, Melissa A.,Cush, Sarah B.,Hammer, Robert P.
, p. 9065 - 9069 (2007/10/03)
The synthesis of O-silyl- and O-acyl-protected furanose glycals from free thymidine was investigated. The method of glycal formation reported by Pedersen et al. was successfully expanded to include 5-ester (toluoyl) protected glycals as well as various combinations of 5'-ester and 3- and 5- tert-butyldimethylsilyl and tert-butyldiphenylsilyl protection. Gram quantities of furanoid glycals can be prepared in a few days in two-four steps in overall yields ranging from 17 to 80%.