Publication | Closed Access
Efficient Modular Synthesis of Isomeric Mono‐ and Bispyridyl[2.2]paracyclophanes by Palladium‐Catalyzed Cross‐ Coupling Reactions
30
Citations
64
References
2016
Year
Chemical EngineeringCross-coupling ReactionDerivativesEfficient Modular SynthesisEngineeringStille CouplingNatural SciencesHeterocyclicDiversity-oriented SynthesisOrganic ChemistryOrganometallic CatalysisCatalysisChemistryVersatile ReactionHeterocycle ChemistryAbstract Pyridyl‐substitutedIsomeric Mono‐Biomolecular Engineering
Abstract Pyridyl‐substituted [2.2]paracyclophanes build a multifunctional structural motif that is useful in material chemistry, catalysis and for luminescent structures. Nonetheless, there is still a lack of general methods for the synthesis of these structures tolerating easily accessible bromides as well as different isomeric pyridyl groups. Hence the coupling of functionalized [2.2]paracyclophanes with various substituted and functionalized pyridyl derivatives was achieved using Stille, Suzuki and Kumada coupling conditions. Hereby the Stille coupling of a [2.2]paracyclophane is presented as a versatile reaction for the formation of heteromeric [2.2]paracyclophane‐containing biaryl structures. magnified image
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