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The title reaction features low catalyst loading and readily available reagents, but it only applies to cyclic amines. [ABSTRACT FROM AUTHOR]

The article presents chemical equations for the article "Cobalt(III)-Catalyzed Annulation of Esters and Alkynes: A Facile Route to Indenones" by W. Yu and others published in "Chemical Communications" in 2016.

This copper-catalyzed tandem decarboxylative cross-coupling/cyclization provides a highly efficient method for preparation of pyrrolidones. [ABSTRACT FROM AUTHOR]

This efficient regioselective cyclization of enamides with alkynes yields various pyrroles. [ABSTRACT FROM AUTHOR]

The title synthesis tolerates a wide range of functional groups and gives the benzyl esters in good yields. [ABSTRACT FROM AUTHOR]

The reaction is successfully extended to aromatic amides to yield various isoindolinones. [ABSTRACT FROM AUTHOR]

A Pd(II)-catalyzed thioether-directed regioselective acetoxylation of arenes is disclosed. [ABSTRACT FROM AUTHOR]

Review: [641 refs. [ABSTRACT FROM AUTHOR]

Efficient Ni-catalyzed direct amination of unactivated arenes with simple alkylamines is achieved with assistance of a bidentate directing group. [ABSTRACT FROM AUTHOR]

48 examples [ABSTRACT FROM AUTHOR]

A simple procedure is elaborated for the nickel-catalyzed aminoquinolinyl-assisted thioetherification of propioamides (I) and (VI). [ABSTRACT FROM AUTHOR]

Abstract: A variety of ketones and internal alkynes are converted into isoquinolines and heterocyclic fused pyridines. [ABSTRACT FROM AUTHOR]

Two reaction systems are evaluated toward the efficient site-selective mono- or dichlorination of substituted 8-acylaminoquinolines. [ABSTRACT FROM AUTHOR]

The article presents chemical equations related to the article "Efficient Synthesis of 1,2,3-Triazoles by Copper-Mediated C—N and N—N Bond Formation Starting From N-Tosylhydrazones and Amines" by Z. Chen and others, published in the "Chemistry: A European Journal" in 2014.

The first rhodium-catalyzed acetoxylation of an olefinic C-H bond in enamides proceeds with high regio- and stereoselectivity to give Z-configurated products. [ABSTRACT FROM AUTHOR]

A series of 2,3-dihydro-1H-indazoles is prepared via a Rh-catalyzed activation of arylhydrazines and olefin addition. The treatment of products (IIIa,f) with HCl in refluxing EtOH leads to 1H-indazoles (IVa,f) in good yields. [ABSTRACT FROM AUTHOR]

The presented three component reaction provides a mild and efficient access to a wide variety of unsaturated amidines of which some might be useful for pharmacological application. [ABSTRACT FROM AUTHOR]

The article presents chemical equations related to the research "Palladium (II)-Catalyzed ortho-Olefination of Arenes Applying Sulfoxides as Remote Directing Groups" by C. Shen and others published in a 2014 issue of the periodical "Organic Letters."

This protocol is compatible with a broad range of functional groups. [ABSTRACT FROM AUTHOR]

The article presents chemical equations related to the article "Silver Ion Promoted, PdII-Catalyzed Arylation of Arenes with a Free Amine as Directing Group in Aqueous Medium" by researcher K. Wang, H. Li, J. Yao and others in the "European Journal of Chemistry" in the 2013 issue.

The article presents chemical equations related to the article "Palladium-Catalyzed Oxidative Acetoxylation of Benzylic C-H Bond Using Bidentate Auxiliary" by L. Ju and others, published in the 2013 issue of the "Journal of Organic Chemistry."

The title method allows the synthesis of ortho-monoarylated or diarylated biaryl-2-amines with exclusive regioselectivity. [ABSTRACT FROM AUTHOR]

A novel protocol for amine directed Pd-catalyzed carbonylation of biaryls (I) is developed. [ABSTRACT FROM AUTHOR]