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RESEARCH PRODUCT
Substrate-dependent fluorinations of highly functionalized cycloalkanes
Attila Márió RemeteLoránd KissSantos FusteroReijo SillanpääFerenc FülöpFerenc FülöpMelinda NonnMelinda Nonnsubject
Steric effectsamino acidsBicyclic molecule010405 organic chemistryChemistryOrganic ChemistryselectivityRegioselectivitydeoxygenation010402 general chemistryRing (chemistry)01 natural sciencesBiochemistryfluorination0104 chemical sciencesCycloalkanechemistry.chemical_compoundNucleophileDrug DiscoveryOrganic chemistrystereoisomersAzideSelectivityta116description
Abstract Substrate-dependent fluorinations of several highly functionalized cycloalkanes with multiple stereocentres were investigated. The synthetic transformations were based on selective functionalization of the ring C C bonds of the readily available bicyclic β-lactams by epoxidation and regioselective nucleophilic oxirane opening with azide or cyanide, followed by hydroxy–fluorine exchange with Deoxofluor. Depending on the substituents and their relative steric arrangement, the attempted fluorinations produced different types of substituted cycloalkanes. These selective, substrate-directed synthetic procedures and their presumed pathways towards interesting highly functionalized fluorinated cycloalkane scaffolds were investigated.
| year | journal | country | edition | language |
|---|---|---|---|---|
| 2016-02-01 | Tetrahedron |