Publication | Closed Access
Regio- and Stereoselective Alkylboration of Endocyclic Olefins Enabled by Nickel Catalysis
88
Citations
89
References
2021
Year
Combinatorial ChemistryEngineeringOrganic ChemistryStereoselective AlkylborationChemistryHeterocycle ChemistryChemical EngineeringMedicinal ChemistrySaturated HeterocyclesOrganometallic CatalysisNickel CatalysisStereoselective SynthesisBiochemistryEndocyclic OlefinsCatalysisAsymmetric CatalysisCatalytic SynthesisAlkene MetathesisNatural SciencesModular AccessSynthetic ChemistryAccessible Drug Motifs
Whereas there is a significant interest in the rapid construction of diversely substituted saturated heterocycles, direct and modular access is currently limited to the mono-, 2,3-, or 3,4-substitution pattern. This Communication describes the straightforward and modular construction of 2,4-substituted saturated heterocycles from readily available materials in a highly stereo- and regioselective manner, which sets the stage for numerous readily accessible drug motifs. The strategy relies on chain walking catalysis.
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