Publication | Closed Access
Gold-Catalyzed Stereoselective Synthesis of Azacyclic Compounds through a Redox/[2 + 2 + 1] Cycloaddition Cascade of Nitroalkyne Substrates
134
Citations
21
References
2011
Year
Chemical EngineeringEngineeringHeterocyclicNitroalkyne SubstratesAzacyclic CompoundsDiversity-oriented SynthesisNatural SciencesCore StructuresOrganic ChemistryNew Redox/cycloaddition CascadeOrganometallic CatalysisCatalysisStereoselective SynthesisChemistryComplex Azacyclic CompoundsHeterocycle ChemistryGold-catalyzed Stereoselective Synthesis
We report a new redox/cycloaddition cascade on readily available 1-alkynyl-2-nitrobenzenes that produces complex azacyclic compounds stereoselectively. The core structures of the resulting products are constructed through a formal [2 + 2 + 1] cycloaddition among α-carbonyl carbenoids, nitroso species, and external alkenes.
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