6533b86efe1ef96bd12cb549
RESEARCH PRODUCT
Selective nitrile oxide dipolar cycloaddition for the synthesis of highly functionalized β-aminocyclohexanecarboxylate stereoisomers
Loránd KissFerenc FülöpFerenc FülöpMelinda NonnMelinda NonnReijo Sillanpääsubject
chemistry.chemical_classificationNitrileBicyclic moleculeStereochemistryOrganic ChemistryOxideIodolactonizationRegioselectivityBiochemistryCycloadditionchemistry.chemical_compoundchemistryDrug DiscoveryOrganic chemistryta116Lactonedescription
Highly functionalized β-aminocyclohexanecarboxylate regio- and stereoisomers were synthesized from a bicyclic β-lactam by successive regioselective iodolactonization, stereo- and regioselective nitrile oxide cycloaddition, lactone ring-opening and isoxazoline ring-opening.
year | journal | country | edition | language |
---|---|---|---|---|
2012-12-01 | Tetrahedron |