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Zinc‐Catalyzed Selective Reduction of Cyclic Imides with Hydrosilanes: Synthesis of ω‐Hydroxylactams
26
Citations
134
References
2015
Year
Excellent RegioselectivityChemical EngineeringAbstract Cyclic ImidesCyclic ImidesEngineeringCatalytic ProtocolOrganic ChemistryOrganometallic CatalysisCatalysisChemistrySynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringSelective Reduction
Abstract Cyclic imides were selectively reduced to the corresponding ω‐hydroxylactams in high yields with (EtO) 3 SiH (triethoxysilane) or PMHS (polymethylhydrosiloxane) under catalysis of zinc diacetate dehydrate [Zn(OAc) 2 ⋅2 H 2 O] (10%) and tetramethylethylenediamine (TMEDA) (10%). This catalytic protocol showed good functional group tolerance as well as excellent regioselectivity for unsymmetrical imides bearing coordinating groups adjacent to the carbonyl. magnified image
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