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Journal ArticleDOI

Copper‐Mediated and Catalyzed C‐H Bond Amination via Chelation‐Assistance : Scope, Mechanism and Synthetic Applications

Jiao Ma, +4 more
- 18 Jan 2022 - 
- Vol. 40, Iss: 10, pp 1204-1223
TLDR
In this article , the research progress of copper-catalyzed C-H amination in recent years is summarized and reaction mechanisms are also briefly described in representative aminations to provide insights for the development prospects of highly practical and more environmentally benign processes.
Abstract
Nitrogen-containing compounds are ubiquitously found in the fields of organic chemistry, pharmaceuticals, agrochemicals, medicinal chemistry and functional materials. The C—H bond amination reaction is one of the most straightforward protocols in the C—N bond formation, showing "step" and "atomic" economy. As a catalyst for C—H amination reaction, copper exhibits its unique catalytic properties due to easily accessible oxidation states. The research progress of copper-catalyzed C—H amination in recent years is summarized. At the same time, reaction mechanisms are also briefly described in representative aminations to provide insights for the development prospects of highly practical and more environmentally benign processes.

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Citations
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Journal ArticleDOI

Selective Mono- and Diamination of Ketones in a Combined Copper–Organocatalyst System

- 13 May 2022 - 
TL;DR: In this paper , a simple and mild protocol for the chemoselective mono-and diamination of ketone using pyrazole as the amine source in a combined copper-organocatalyst system is presented.
Journal ArticleDOI

Copper catalysed α-functionalization of ketones with nucleophile: A universal and efficient access to nafimidone derivatives†

TL;DR: In this article , the authors report the discovery of a convenient and efficient approach to construct various C-X bonds using a copper catalytic system, which features mild reaction condition and easy formation.
Journal ArticleDOI

Copper-Catalyzed C7-Selective C-H/N-H Cross-Dehydrogenative Coupling of Indolines with Sulfoximines.

TL;DR: Cu-catalyzed cross-dehydrogenative coupling of the C7 C-H bond of indolines with sulfoximines has been accomplished and the reaction can be extended to the cross- dehydrogenatives coupling of N-aryl 7-azaindoles with monoselectivity.
Journal ArticleDOI

Directing group strategies in rhodium-catalyzed C-H amination.

TL;DR: In this paper , the reactivity and selectivity of chelation-assisted rhodium-catalyzed C-H amination are discussed in relation to the types of aminating reagent, as well as the challenges and future development prospects in this field.
Journal ArticleDOI

Pd-Catalyzed Aryl C-H Amination with Diaziridinone.

TL;DR: In this paper , an efficient Pd-catalyzed ortho-C-H amination of N-(quinolin-8-yl)benzamides with di-t-butyldiaziridinone, providing a variety of anthranilic amides in good yields.
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

Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: versatility and practicality.

TL;DR: A review of palladium-catalyzed coupling of CH bonds with organometallic reagents through a PdII/Pd0 catalytic cycle can be found in this paper.
Journal ArticleDOI

How many drug targets are there

TL;DR: A consensus number of current drug targets for all classes of approved therapeutic drugs is proposed, and an emerging realization of the importance of polypharmacology and also the power of a gene-family-led approach in generating novel and important therapies is highlighted.
Journal ArticleDOI

Rhodium-Catalyzed C-C Bond Formation via Heteroatom-Directed C-H Bond Activation

TL;DR: This review focuses on Rh-catalyzed methods for C-H bond functionalization, which have seen widespread success over the course of the last decade and are discussed in detail in the accompanying articles in this special issue of Chemical Reviews.
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