Publication | Closed Access
Free Radical-Mediated Vinyl Amination: Access to <i>N,N</i>-Dialkyl Enamines and Their β-Stannyl and β-Thio Derivatives
39
Citations
11
References
2002
Year
β-Thio DerivativesEnantioselective SynthesisEngineeringRadical (Chemistry)N-dialkyl EnaminesOrganic ChemistryConvenient Synthetic AccessStereoselective SynthesisChemistryHeterocycle ChemistrySynthetic ChemistryBiomolecular EngineeringTandem Bond-forming Processes
[reaction: see text] The first examples of free radical-mediated vinyl amination are described by nonconventional vinyl radical addition to azomethine nitrogen. This new vinyl amination protocol is mild and provides convenient synthetic access to nonstabilized N,N-dialkyl enamines and tandem bond-forming processes.
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