Publication | Open Access
Diastereoselective Aminooxygenation and Diamination of Alkenes with Amidines by Hypervalent Iodine(III) Reagents
66
Citations
71
References
2014
Year
EngineeringAlkene MetathesisHypervalent IodineOrganic ChemistryDiastereoselective AminooxygenationCatalysisPresent Transformation OffersChemistryDiastereoselective Anti-aminooxygenationHeterocycle ChemistryStereoselective SynthesisOrganometallic CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
Diastereoselective anti-aminooxygenation and anti-diamination of alkenes with amidines were enabled by hypervalent iodine(III) reagents such as PhI(OCOR)2 and PhI(NMs2)2, respectively. The present transformation offers diastereochemically pure dihydroimidazoles divergently from E- and Z-alkenes.
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