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anti-Selective aminofluorination of alkenes with amidines mediated by hypervalent iodine(<scp>iii</scp>) reagents
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Citations
42
References
2015
Year
HalogenationEngineeringAlkene MetathesisHypervalent IodineFluorous SynthesisOrganic ChemistryChemistryAnti-selective AminofluorinationHeterocycle Chemistry3-Fluoropropane-1,2-diamine DerivativesBiomolecular Engineering
anti-Selective aminofluorination of alkenes with amidines was enabled by hypervalent iodine(iii) reagents, affording 4-fluoroalkyl-2-imidazolines. Further reductive ring-opening of the 2-imidazoline moiety could deliver highly functionalized 3-fluoropropane-1,2-diamine derivatives.
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