915694-40-5

Upstream product

• 303963-92-0 (3aR,6aR)-6-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyl-3a,6a-dihydro-4H-cyclopenta[d][1,3]dioxol-4-one 
• 303963-93-1 (3aS,4S,6aR)-6-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyl-3a,6a-dihydro-4H-cyclopenta[d][1,3]dioxol-4-ol 
• 915694-38-1 (3aR,3bR,4aS,5S,5aS)-3b-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethylhexahydrocyclopropa[3,4]cyclopenta[1,2-d][1,3]dioxol-5-ol 
• 915694-39-2 (+)-(1S,2S,3S,4R,5R)-4-tert-butoxy-5-(tert-butyldiphenylsilyloxymethyl)bicyclo[3.1.0]hexane-2,3-diol 
• 58479-61-1 tert-butylchlorodiphenylsilane 

Downstream Products

• 915694-42-7 (+)-(1R,2R,3R,4S,5S)-2-tert-butoxy-4-(tert-butyldiphenylsilyloxy)-1-(tert-butyldiphenylsilyloxymethyl)-3-methyl-bicyclo[3.1.0]hexan-3-ol 
• 915694-41-6 (+)-(1R,2R,4S,5S)-2-tert-butoxy-4-(tert-butyldiphenylsilyloxy)-1-(tert-butyldiphenylsilyloxymethyl)-bicyclo[3.1.0]hexan-3-one 

Relevant academic research and scientific papers

Asymmetric synthesis of cyclopropyl-fused 2′-C-methylcarbanucleosides as potential anti-HCV agents

Novel 2′-C-methyl-cyclopropyl-fused carbocyclic nucleosides as potential anti-HCV agents were stereoselectively synthesized, utilizing regioselective cleavage of the isopropylidene group and cyclic sulfate chemistry as key steps. Copyright Taylor & Franci

Stereoselective synthesis of 2′-C-methyl-cyclopropyl-fused carbanucleosides as potential anti-HCV agents

(Chemical Equation Presented) Stereoselective synthesis of 2′-C-methyl-cyclopropyl-fused carbanucleosides was accomplished via stereoselective cyclopropanation, regioselective cleavage of the isopropylidene group, stereoselective Grignard reaction, and cy