6533b86efe1ef96bd12cb549

RESEARCH PRODUCT

Selective nitrile oxide dipolar cycloaddition for the synthesis of highly functionalized β-aminocyclohexanecarboxylate stereoisomers

Loránd KissFerenc FülöpFerenc FülöpMelinda NonnMelinda NonnReijo Sillanpää

subject

chemistry.chemical_classificationNitrileBicyclic moleculeStereochemistryOrganic ChemistryOxideIodolactonizationRegioselectivityBiochemistryCycloadditionchemistry.chemical_compoundchemistryDrug DiscoveryOrganic chemistryta116Lactone

description

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.

10.1016/j.tet.2012.09.085https://doi.org/10.1016/j.tet.2012.09.085