Publication | Closed Access
Visible-Light-Catalyzed [3 + 1 + 2] Coupling Annulations for the Synthesis of Unsymmetrical Trisubstituted Amino-1,3,5-triazines
32
Citations
55
References
2019
Year
Unsymmetrical Trisubstituted Amino-1,3,5-triazinesMedicinal ChemistryCross-coupling ReactionEngineeringPhotochemistryNatural SciencesLigand-free ConditionsDiversity-oriented SynthesisOrganic ChemistryWide Substrate ScopesCatalysisChemistryHeterocycle ChemistryAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
A visible-light catalyzed [3 + 1 + 2] annulation for the synthesis of unsymmetrical trisubstituted amino-1,3,5-triazines from amidines, isothiocyanates, and 1,1,3,3-tetramethylguanidines has been developed. This method exhibits the advantages of easily available starting materials, insensitive to air and moisture, wide substrate scopes, high step economy, mild, metal- and ligand-free conditions, which has potential applications in the organic, medicinal, and material chemistry.
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