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Peri-, Chemo-, Regio-, Stereo- and Enantio-Selectivities of 1,3-dipolar cycloaddition reaction of C,N-Disubstituted nitrones with disubstituted 4-methylene-1,3-oxazol-5(4H)- one: A quantum mechanical study

George Baffour Pipim, Ernest Opoku, Richard Tia, Evans Adei

2020Journal of Molecular Graphics and Modelling21 citationsDOI

Topics & Concepts

ElectrophileChemistryCycloadditionMethyleneNatural bond orbitalHOMO/LUMOMulliken population analysisNucleophileDensity functional theory1,3-Dipolar cycloadditionMedicinal chemistryDipoleComputational chemistryReactivity (psychology)PhotochemistryOrganic chemistryMoleculeCatalysisPathologyMedicineAlternative medicineOrganic Chemistry Cycloaddition ReactionsChemical Reaction MechanismsSynthesis and Reactions of Organic Compounds
Peri-, Chemo-, Regio-, Stereo- and Enantio-Selectivities of 1,3-dipolar cycloaddition reaction of C,N-Disubstituted nitrones with disubstituted 4-methylene-1,3-oxazol-5(4H)- one: A quantum mechanical study | Litcius