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An abstract of the article "Copper Iodide Mediated Cyanation of Arylboronic Acids and Aryl Iodides with Ethyl (Ethoxymethylene)Cyanoacetate as Cyanating Agent" by C. Qi, X. Hu and H. He is presented.

An abstract of the article "A Highly Efficient CuI Nanoparticles-Catalyzed Synthesis of Tetrahydro-chromenediones and Dihydropyrano(c)chromenediones under Grinding" by S. Abdolmohammadi, R. Ghiasi, and S. Ahmadzadeh-Vatani is presented.

An abstract of the article "Copper Iodide Mediated Cyanation of Arylboronic Acids and Aryl Iodides with Ethyl (Ethoxymethylene)cyanoacetate as Cyanating Agent" by Chaorong Qi and colleagues is presented.

This methodology provides structurally diverse N-arylbenzamides (III) in very good to excellent yields. [ABSTRACT FROM AUTHOR]

The article presents chemical equations related to the article "CuI-Catalyzed Domino Reactions for the Synthesis of Benzoxazine-Fused Isoquinolines under Microwave Irradiation" by Y.-H. Zhao and others, published in the periodical "Synthetic Communications" in 2016.

The reaction proceeds well with benzyl halides and arylalkynes while halobenzenes fail and alkylalkynes (e.g., 1-hexyne and cyclohexylalkyne) give complex mixtures. [ABSTRACT FROM AUTHOR]

A double catalytic cycle mechanism involving elemental iodine and copper is proposed. [ABSTRACT FROM AUTHOR]

An efficient, low-hazard protocol for the reaction of coumarin and quinolone derivatives with phenylthiocyanates is presented. [ABSTRACT FROM AUTHOR]

A diagram is presented showing the synthesis of biaryl thioether through CuI catalyzed dominothiolation of aryl halides in 4-Dimethylaminopyridine (DMAP) presence as ligand.

A diagram is presented which explains the intramolecular N2-arylation catalyzed by the cuprous iodide/L-Proline (CuI/L-Proline) for the synthesis of the Benzo [f]pyrazolo[1,5-a][1,4]diazepin-4-ones and the Benzo [6,7][1,4]diazepino[1,2-b]indazol-7(6H)-ones.

The article presents a chemical reaction of formylpyrroles by using the copper iodide-catalyzed cascade oxidation.

A scalable, efficient, mild, and straightforward method for the synthesis of the title compounds is developed. [ABSTRACT FROM AUTHOR]

The significant advantages of this protocol are high yields, elimination of dangerous and toxic reagents and a simple work-up procedure. [ABSTRACT FROM AUTHOR]

The reaction conditions are unsuitable for the transformation of aminothiazoles, pyrimidines and pyrazines. [ABSTRACT FROM AUTHOR]

The described process gives the title-products in a one-pot fashion through the in situ formation of ynamides followed by intramolecular hydroamidation. [ABSTRACT FROM AUTHOR]

The synthesis of substituted dihydrooxazoles (II) and (IV) by a CuI-catalyzed cycloisomerization of terminal propargyl amides (I) is reported. [ABSTRACT FROM AUTHOR]

It is proposed, that the reaction of tetrahydroisoquinoline with aromatic aldehydes provide exo-iminium ions, which isomerize to endo-iminium ions. [ABSTRACT FROM AUTHOR]

The oxidative cyclocondensation of 2-aminopyridines with aryl alkyl ketones is investigated to provide a synthesis of imidazo[1,2-a]pyridines. [ABSTRACT FROM AUTHOR]

Metformin is a novel, polydentate nitrogen donor ligand that can be used for N/O-arylation reactions along with air-stable and inexpensive copper(I) iodide. [ABSTRACT FROM AUTHOR]

The title reaction is catalyzed by copper iodide. [ABSTRACT FROM AUTHOR]

The reaction proceeds without obvious racemization. [ABSTRACT FROM AUTHOR]

A ligand-free protocol consisting of alkylation of propargylamines (II) with benzyl bromides of type (I) and subsequent intramolecular CuI-catalyzed azide alkyne 1,3-dipolar cycloaddition offers a simple approach to triazolo-fused benzodiazepines (III). [ABSTRACT FROM AUTHOR]

In the presence of CuI and Pd(PPh3)4 as catalyst, title compounds are predominantly obtained as (E)-isomers whereby, (Z)-products are supposed to be formed during the isolation by isomerization. [ABSTRACT FROM AUTHOR]

The reaction proceeds through C-H activation with oxidative linkage of two C-N bonds under mild conditions and oxygen as a sole oxidant. [ABSTRACT FROM AUTHOR]

A diagram is presented which explains the synthesis of thiophosphates catalyzed by copper(I) iodide through Hydrogen (H)-phosphates with benzenethiols.

The article presents a chemical reaction formula for one-pot synthesis of dibenzodiazepinones via copper (I) iodide (CuI) catalysis in ethylene glycol.

In this article, the authors present chemical equations related to the chemoselective carbonyl allylation of chalcones with allyltributylstannane catalyzed by copper(I) iodide published in the journal "Tetrahedron Letters" in 2013.

A short synthesis of ethylacetoacetate tagged imidazolium ionic liquids is described and the utility of the compounds as functional solvent for the CuI-nanoparticle promoted direct amination of aryl halides is demonstrated. [ABSTRACT FROM AUTHOR]

The catalyst can be recovered by simple filtration and reused up to 10 consecutive runs without loss of its efficiency. [ABSTRACT FROM AUTHOR]

Colorless needle-like crystals of α-(NMe4)[Cu2I3] are prepared by solvothermal reaction of CuI, hexamethylenetetramine, and HI in MeOH in a molar ratio of 5:2:7:150 (autoclave, 150 °C, 120 h; 61% yield). [ABSTRACT FROM AUTHOR]

A series of new N-arylanthranilic acids of type (III) are prepared from 2-chlorobenzoic acids and sterically hindered aniline derivatives using copper(I) iodide as catalyst. [ABSTRACT FROM AUTHOR]