511549-98-7

Upstream product

• 511549-97-6 3-benzoyl-1-[6-(tert-butyl-dimethyl-silanyloxy)-spiro[4.4]non-2-yl]-5-methyl-1H-pyrimidine-2,4-dione 
• 4330-20-5 N-3-benzoylthymine 
• 511549-91-0 tert-Butyl-dimethyl-((1S,5R)-spiro[4.4]non-6-en-1-yloxy)-silane 
• 511549-94-3 (2R,5R,6S)-6-(tert-Butyl-dimethyl-silanyloxy)-spiro[4.4]nonan-2-ol 
• 511549-92-1 (2S,5R,6S)-6-(tert-Butyl-dimethyl-silanyloxy)-spiro[4.4]nonan-2-ol 
• 511549-93-2 Benzoic acid (2R,5R,6S)-6-(tert-butyl-dimethyl-silanyloxy)-spiro[4.4]non-2-yl ester 

Relevant academic research and scientific papers

Conversion of the enantiomers of spiro[4.4]nonane-1,6-diol into both epimeric carbaspironucleosides having natural C1′ absolute configuration

(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.