Publication | Closed Access
Highly Efficient Activation of Organosilanes with η<sup>2</sup>-Aldehyde Nickel Complexes: Key for Catalytic Syntheses of Aryl-, Vinyl-, and Alkynyl-Benzoxasiloles
39
Citations
74
References
2014
Year
Inorganic ChemistryChemical EngineeringNovel OrganocatalystsEngineeringCross-coupling ReactionCatalytic SynthesesHighly Efficient ActivationHypervalent Silicate ReactantEffective ActivatorOrganic ChemistryOrganometallic CatalysisCatalysis-Aldehyde ComplexChemistrySynthetic Chemistry
An η(2)-aldehyde nickel complex was utilized as an effective activator for an organosilane in order to generate a hypervalent silicate reactant for the first time. This method was successfully applied to the highly efficient syntheses of 3-aryl-, vinyl-, and alkynyl-2,1-benzoxasiloles from benzaldehydes with aryl-, vinyl-, and alkynylsilyl groups at the ortho position. Initial mechanistic studies revealed that an intermolecular aryl transfer process was involved in the reaction mechanism. The formation of an η(2)-aldehyde complex was directly confirmed by NMR.
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