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Metal-Free Oxidative Spirocyclization of Alkynes with Sulfonylhydrazides Leading to 3-Sulfonated Azaspiro[4,5]trienones
128
Citations
65
References
2015
Year
Natural Product SynthesisEngineeringHeterocyclicOrganic ChemistrySequential SulfonylationCatalysisChemistryHeterocycle ChemistryPharmacologyMetal-free Oxidative SpirocyclizationSynthetic ChemistryBiological ImportanceDirect Oxidative Spirocyclization
A novel and direct oxidative spirocyclization of arylpropiolamides with sulfonylhydrazides leading to 3-sulfonated azaspiro[4,5]trienones has been developed under metal-free conditions. The reaction is performed in a tandem manner constituted by the sequential sulfonylation of alkynes, ipso-carbocyclization, dearomatization, hydration, and oxidation processes, providing a convenient and efficient approach to various sulfonated azaspiro[4,5] trienones of biological importance.
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