Publication | Closed Access
Pd-Catalyzed Heck-Type Cascade Reactions with <i>N</i>-Tosyl Hydrazones: An Efficient Way to Alkenes via in Situ Generated Alkylpalladium
98
Citations
52
References
2013
Year
Aryl HalidesCross-coupling ReactionEngineeringAlkene MetathesisNeopentylpalladium SpeciesOrganic ChemistryOrganometallic CatalysisCatalysisMolecular CatalysisChemistrySpiro CompoundsAsymmetric CatalysisBiomolecular EngineeringSitu Generated AlkylpalladiumEfficient Way
A palladium-catalyzed Heck-type cascade reaction of aryl halides and N-tosyl hydrazones is reported. The neopentylpalladium species, generated from an intramolecular Heck-type insertion reaction of aryl halides, could efficiently react with carbenes to form highly functionalized alkenes. The synthesis of spiro compounds was also explored via a multiple Heck-type insertion reaction with N-tosyl hydrazone.
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