1268630-06-3Relevant academic research and scientific papers
Two convergent approaches toward novel carbocyclic C-nucleosides
Nencka, Radim,Sala, Michal,Dejmek, Milan,Drainsky, Martin,Holy, Antonin,Hebabecky, Hubert
supporting information; experimental part, p. 4119 - 4130 (2011/02/22)
Two convergent methodologies for construction of novel carbocyclic C-nucleosides allowing the syntheses of derivatives with uracil heterobase substituted at the position C-5 as well as C-6 were developed. The crucial step of the first methodology was the
Model synthesis of six-membered carbocyclic spironucleosides
Nencka, Radim,Hrebabecky, Hubert,Dracinsky, Martin
experimental part, p. 1259 - 1272 (2011/08/21)
Model study focusing on the synthesis of carbocyclic spironucleosides is presented. Hydantoin base was built on the easily accessible ketone precursors by Bucherer-Bergs reaction. On saturated substrates the reaction proceeded smoothly. On α,β-unsaturated
