Publication | Open Access
1,2,3-Triazole Formation under Mild Conditions via 1,3-Dipolar Cycloaddition of Acetylenes with Azides
118
Citations
18
References
2003
Year
Chemical EngineeringEngineeringHeterocyclicReaction Tem Perature1,2,3-Triazole FormationNatural SciencesDiversity-oriented SynthesisMild Conditions1,3-Dipolar CycloadditionOrganic Chemistry1,3-Dipolar Cycloadditio NSynthetic ChemistryChemistryHeterocycle ChemistryReaction TemperatureEnantioselective Synthesis
1,3-Dipolar cycloadditio n of azides to various electron-withdrawing group substituted acetylenes lead ing to triazole for mation under mild conditions (reaction temperature around 55 °C or below ) are reviewed.Furtherm ore, our efforts to lo wer the reaction tem perature of cycloaddition of acetylenic am ides with azides have also been discussed.
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