Publication | Closed Access
Regioselective iodoamination of terminal ynamides for the synthesis of α-amino-β,β-diiodo-enamides
25
Citations
39
References
2016
Year
Terminal AlkynesEfficient MethodologyEngineeringTerminal YnamidesI2/tbhp-mediated Intermolecular IodoaminationOrganic ChemistryChemistryAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
A mild and efficient methodology involving the I2/TBHP-mediated intermolecular iodoamination of ynamides with amines for the synthesis of α-amino-β,β-diiodo-enamides was developed. This reaction provides the first intermolecular iodoamination of terminal alkynes to diiodo-enamines and can be easily applied to a wide range of substrates.
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