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3d Transition Metals for C-H Activation.

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TLDR
A comprehensive overview on first row transition metal catalysts for C-H activation until summer 2018 is provided.
Abstract
C–H activation has surfaced as an increasingly powerful tool for molecular sciences, with notable applications to material sciences, crop protection, drug discovery, and pharmaceutical industries, among others. Despite major advances, the vast majority of these C–H functionalizations required precious 4d or 5d transition metal catalysts. Given the cost-effective and sustainable nature of earth-abundant first row transition metals, the development of less toxic, inexpensive 3d metal catalysts for C–H activation has gained considerable recent momentum as a significantly more environmentally-benign and economically-attractive alternative. Herein, we provide a comprehensive overview on first row transition metal catalysts for C–H activation until summer 2018.

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Journal ArticleDOI

Metal-Organic Framework-Based Catalysts with Single Metal Sites.

TL;DR: This review overviews the recent developments of catalysis at single metal sites in MOF-based materials with emphasis on their structures and applications for thermocatalysis, electrocatalysis, and photocatalysis.
Journal ArticleDOI

N-Heterocyclic Carbene Complexes in C–H Activation Reactions

TL;DR: Through discussing the role of NHC ligands in promoting challenging C-H activation methods, the reader is provided with an overview of this important area and its crucial role in forging carbon-carbon and carbon-heteroatom bonds by directly engaging ubiquitous C- H bonds.
Journal ArticleDOI

Enantioselective C-H Activation with Earth-Abundant 3d Transition Metals.

TL;DR: The remarkable recent progress in enantioselective transformations via organometallic C-H activation by 3d base metals until April 2019 is discussed.
Journal ArticleDOI

Recent advances in the synthesis of axially chiral biaryls via transition metal-catalysed asymmetric C–H functionalization

TL;DR: An overview of recent advances in the synthesis of axially chiral biaryl motifs via transition metal-catalysed asymmetric C-H functionalization is provided.
Journal ArticleDOI

C-H Activation: Toward Sustainability and Applications.

TL;DR: In this article, the authors highlight the research areas seeking to overcome the sustainability challenges of C-H activation: the pursuit of abundant metal catalysts, the avoidance of static directing groups, the replacement of metal oxidants, and the introduction of bioderived solvents.
References
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Journal ArticleDOI

Cationic Cobalt(III) Catalyzed Indole Synthesis: The Regioselective Intermolecular Cyclization of N-Nitrosoanilines and Alkynes

TL;DR: The unique regioselectivity and reactivity of cobalt(III) in the direct cyclization of N-nitrosoanilines with alkynes for the expedient synthesis ofN-substituted indoles is demonstrated.
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Potentiality of vanadium compounds as anti-parasitic agents

TL;DR: A review of vanadium-based potential anti-parasitic agents, mainly active against the parasites causing American trypanosomiasis (Chagas disease), leishmaniasis and amoebiasis, is presented in this paper.
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Application of Langlois’ Reagent in Trifluoromethylation Reactions

TL;DR: A review of radical trifluoromethylation reactions with CF3SO2Na as a CF3 source can be found in this paper, where the authors examine the recent advances in radical triplicate trifluromethynylation reaction with CF 3SO2 Na as a source.
Journal ArticleDOI

Cobalt(III)-Catalyzed Aryl and Alkenyl C-H Aminocarbonylation with Isocyanates and Acyl Azides.

TL;DR: Expedient C-H aminocarbonylations of unactivated (hetero)arenes and alkenes were accomplished with a cobalt(III) catalyst that shows high functional group tolerance and enabled step-economical reactions with isocyanates or acyl azides.
Journal ArticleDOI

Cobalt-Catalyzed Benzylic Borylation: Enabling Polyborylation and Functionalization of Remote, Unactivated C(sp3)–H Bonds

TL;DR: Cobalt dialkyl and bis(carboxylate) complexes bearing α-diimine ligands have been synthesized and demonstrated as active for the C(sp(3))-H borylation of a range of substituted alkyl arenes using B2Pin2 (Pin = pinacolate) as the boron source.
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