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When Organocatalysis Meets Transition‐Metal Catalysis

European Journal of Organic Chemistry · 2010 · Vol. 2010(16) · pp. 2999–3025
Cheng ZhongXiaodong Shi

Abstract

Abstract In the past several years, applications of transition metal complexes in tuning the reactivity of organocatalyst‐promoted transformations have attracted increasing attention in the synthetic community. Efforts in this direction have led to the discovery of unprecedented reactivities, which are not accessible through the use of either of these two catalytic systems separately. The concept continues to develop and offers huge potential. This microreview describes and summarizes recent progress in this field, focusing on discussion of the enhancement and diversification of reactivity patterns in organocatalysis through the deployment of transition metal complexes.

Asymmetric Hydrogenation and CatalysisAsymmetric Synthesis and CatalysisCatalytic C–H Functionalization MethodsChemistryOrganocatalysisReactivity (psychology)Transition metalCatalysisDiversification (marketing strategy)Combinatorial chemistryNanotechnologyBiochemical engineeringOrganic chemistry
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References
Proline-Catalyzed Direct Asymmetric Aldol Reactions
Journal of the American Chemical Society · 2000 · 2,809 citations
Recent Advances in Asymmetric Organocatalytic 1,4‐Conjugate Additions
European Journal of Organic Chemistry · 2007 · 1,145 citations
In the Golden Age of Organocatalysis
Angewandte Chemie International Edition · 2004 · 2,568 citations
Stability and reactivity of N-heterocyclic carbene complexes
Coordination Chemistry Reviews · 2004 · 982 citations
Asymmetric synthesis of bicyclic intermediates of natural product chemistry
The Journal of Organic Chemistry · 1974 · 1,224 citations
Proline-catalyzed asymmetric reactions
Tetrahedron · 2002 · 1,146 citations
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