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Cobalt-Catalyzed Asymmetric Cyclopropanation of Electron-Deficient Olefins
232
Citations
23
References
2007
Year
Chemical EngineeringEngineeringCobalt-catalyzed Asymmetric CyclopropanationAlkene MetathesisDiazo CompoundsEffective CatalystOrganic ChemistryOrganometallic CatalysisCatalysisChemistryAsymmetric CatalysisOne-pot ProtocolEnantioselective Synthesis
The cobalt(II) complex of a D2-symmetric chiral porphyrin [Co(1)] is an effective catalyst for asymmetric cyclopropanation of electron-deficient olefins, including α,β-unsaturated esters, amides, ketones, and nitriles. Due to the absence of dimerization of diazo compounds, the catalytic reactions can be performed in one-pot protocol using olefins as the limiting reagent, forming the desired electrophilic cyclopropane derivatives in high yields and selectivities under mild conditions. In most cases, both excellent diastereo- and enantioselectivity were achieved.
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