511549-86-3Relevant academic research and scientific papers
Direct comparison of SN2 mesylate displacement versus the mitsunobu protocol for 2′,3′-dideoxyspirocarbanucleoside construction
Hartung, Ryan E.,Paquette, Leo A.
, p. 75 - 78 (2007/10/03)
The two title reactions have been evaluated in order to maximize the efficiency with which pyrimidine and purine nucleobases can be introduced into 2′,3′-dideoxyspirocarbanucleosides.
Conversion of the enantiomers of spiro[4.4]nonane-1,6-diol into both epimeric carbaspironucleosides having natural C1′ absolute configuration
Paquette, Leo A.,Hartung, Ryan E.,France, David J.
, p. 869 - 871 (2007/10/03)
(Matrix presented) The enantiomers of spiro[4.4]nonane-1,6-diol have been transformed by different reaction pathways into the two possible carbaspironucleoside epimers with natural C1′ absolute stereochemistry.
