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A simple approach to 1′,1′a-methano carbocyclic thymidine
21
Citations
14
References
1995
Year
Chiral 2-Benzyloxymethylcyciopent-3-enolEngineeringBiochemistryNatural SciencesDiversity-oriented Synthesis1′,1′A-methano Carbocyclic ThymidineOrganic ChemistrySimple ApproachStereoselective SynthesisChemistryHeterocycle ChemistryAsymmetric CatalysisDerivative (Chemistry)Synthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringRigid Molecule
An enantioselective synthesis of 1′,1′a-methano carbocyclic thymidine, a rigid molecule that mimics thymidine's 2′-endo/3′-exo(South) conformation, is efficiently synthesized from chiral 2-benzyloxymethylcyciopent-3-enol.
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