Publication | Closed Access
Easy Access to 3- or 5-Heteroarylamino-1,2,4-triazines by S<sub>N</sub>Ar, S<sub>N</sub><sup>H</sup>, and Palladium-Catalyzed N-Heteroarylations
58
Citations
35
References
2004
Year
Wide VarietyEngineeringHeteroaryl CompoundsHeterocyclicOrganic ChemistryCatalysisEasy AccessChemistryAnionic ProcessesHeterocycle ChemistrySynthetic ChemistryBiomolecular EngineeringPalladium-catalyzed N-heteroarylations
In this paper, N-arylations between two heteroaryl compounds were studied. Conditions were found to generate selectively either 3- or 5-heteroarylamino-1,2,4-triazines by investigating anionic processes (use of bases such as 2,2',6,6'-tetramethylpiperidine/tBuOK/nBuLi) or Pd-catalyzed N-arylations [Pd(OAc)(2), xantphos]. These methods were successfully applied to a wide variety of heteroarylamines and allowed us to pursue our work on fused polynitrogen compounds synthesis.
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