156126-13-5Relevant articles and documents
4',6'-Methano carbocyclic thymidine: A conformationally constrained building block for oligonucleotides
Altmann,Kesselring,Francotte,Rihs
, p. 2331 - 2334 (1994)
The synthesis of the title compound 1 has been accomplished in 20 chemical steps starting from D-ribonolactone. X-ray crystallography shows the bicyclic skeleton of 1 to adopt a boat-like ('2'-exo') conformation and preliminary hybridization data indicate
Synthesis and anti-HIV activity of carbocyclic ring-enlarged 4′,1′a-methano oxetanocin analogues
Jeong, Lak S.,Bae, Min,Chun, Moon W.,Marquez, Victor E.
, p. 1059 - 1062 (2007/10/03)
Synthesis of carbocyclic ring-enlarged 4′,1′a-methano oxetanocin analogues via completely regioselective opening of cyclic sulfites by sodium azide or purine bases is described. Copyright