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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

Carbon Dioxide Hydrogenation to Formate Catalyzed by a Bench-Stable, Non-Pincer-Type Mn(I) Alkylcarbonyl Complex.

TL;DR: The well-defined, bench-stable alkylcarbonyl Mn(I) bis(phosphine) complex was tested as an efficient and selective non-precious-metal precatalyst for the hydrogenation of CO2 to formate under mild conditions.
Journal ArticleDOI

Exploiting Strained Rings in Chelation Guided C‐H Functionalization: Integration of C‐H Activation with Ring Cleavage

TL;DR: This review will focus on recent developments in transition-metal catalyzed chelation assisted concomitant C-H activation and ring scission of strained rings to attain molecular complexity.
Journal ArticleDOI

Synthesis of benzoazepine derivatives via Rh(III)-catalyzed inert C(sp2)–H functionalization and [4 + 3] annulation

TL;DR: With this method, a series of hybrid compounds combining the biologically promising imidazole and benzoazepine moieties decorated with a synthetically versatile carboxyl group were prepared in moderate to good efficiency and the utility was remarkably showcased by their efficient transformations into some otherwise difficult-to-obtain pentacyclic compounds.
Journal ArticleDOI

Peroxide-mediated site-specific C–H methylation of imidazo[1,2-a]pyridines and quinoxalin-2(1H)-ones under metal-free conditions

TL;DR: Methylated imidazopyridines and quinoxalin-2(1H)-ones were smoothly synthesized in moderate to good yields and a free radical reaction mechanism was proposed to describe the methylation process.
Journal ArticleDOI

Cobalt-catalyzed dehydrogenative functionalization of alcohols: Progress and future prospect

TL;DR: In this article , the advancement in cobalt-catalyzed, both homogeneous and heterogeneous, dehydrogenation of alcohols, numerous CC and CN bond formation reactions, synthesis of heterocycles, and other valuable products formation following the borrowing hydrogen (BH) and acceptorless dehydrogenative coupling (ADC) strategy.
References
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Journal ArticleDOI

Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions

TL;DR: This is the first comprehensive review encompassing the large body of work in this field over the past 5 years, and will focus specifically on ligand-directed C–H functionalization reactions catalyzed by palladium.
Journal ArticleDOI

Fluorine in Pharmaceuticals: Looking Beyond Intuition.

TL;DR: Experimental progress in exploration of the specific influence of carbon-fluorine single bonds on docking interactions is reviewed and complementary analysis based on comprehensive searches in the Cambridge Structural Database and the Protein Data Bank is added.
Book ChapterDOI

Heavy metal toxicity and the environment.

TL;DR: This review provides an analysis of arsenic, cadmium, chromium, lead, and mercury's environmental occurrence, production and use, potential for human exposure, and molecular mechanisms of toxicity, genotoxicity, and carcinogenicity.
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Understanding TiO2 photocatalysis: mechanisms and materials.

TL;DR: This paper presents a meta-analyses of the chiral stationary phase transition of Na6(CO3)(SO4)2, Na2SO4, and Na2CO3 of the Na2O/Na2O 2 mixture at the stationary phase and shows clear patterns in the response of these two materials to each other.
Journal ArticleDOI

Organic Photoredox Catalysis

TL;DR: An overview of the basic photophysics and electron transfer theory is presented in order to provide a comprehensive guide for employing this class of catalysts in photoredox manifolds.
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