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A novel method for the synthesis of β-arylsulfonyl enamines (III), (VI) and (VIII)/(IX) via photoredox catalysis is reported. [ABSTRACT FROM AUTHOR]

The article presents chemical structure for N-H imines and alkynes.

The two-step procedure gives access to the title compounds starting from iodo salicylate (I) and a broad variety of arylboronic acids within a very short time and good to excellent yields. [ABSTRACT FROM AUTHOR]

A graphical abstract of the article "Morita-Baylis-Hillman Reaction of α,β-Unsaturated Ketones with Allylic Acetates by the Combination of Transition-Metal Catalysis and Organomediation" is presented.

A range of N-arylglycine esters react with variously functionalized phenol derivatives in an ortho-selective manner. [ABSTRACT FROM AUTHOR]

A diagram is presented showing the regioselective dehydrogenative and highly chemoselective cross-coupling reaction between ethers and pyridines.

A novel dehydrogenative cross-coupling reaction of methylquinoline derivatives with N-aryl glycine esters under the cooperative catalysis of copper salt and a Broensted acid is developed. [ABSTRACT FROM AUTHOR]

The article presents chemical equations related to the article "Copper-Catalyzed Dehydrogenative Cross-Coupling Reaction Between Unactivated Ethers and Simple Ketones Mediated by Pyrrolidine" by Zhi-Zhen Huang et al published in the journal "Angewandte Chemie International Edition" in 2014.

Various aromatic aldehydes and N-substituted N-heteroarene-2-carboxamides react effectively to generate secondary imides tolerating a wide range of functionalities. [ABSTRACT FROM AUTHOR]

This Pd-catalyzed and ester-directed ortho-olefination of phenyl acetic and propionic esters offers a new way to modify aromatic-containing aliphatic acids. Olefinated heterocyclic acetic and propionic acid esters are also obtained in good yields. Extension to benzoic acid derivatives and up-scaling complete this new protocol. [ABSTRACT FROM AUTHOR]

The reaction has a good functional group tolerance and can be scaled up. [ABSTRACT FROM AUTHOR]

The scalable title reaction offers access to various 3,4-dihydroisoquinoline derivatives in high yields. [ABSTRACT FROM AUTHOR]

A new domino Heck-isomerization/Saegusa/Heck reaction of propenol with various aryl iodides is reported for the synthesis of 3,3-diaryl propenals by transition-metal catalysis. [ABSTRACT FROM AUTHOR]

The article presents chemical equations related to the article "Palladium-Catalyzed Oxalyl Amide-Directed γ-Arylation of Aliphatic Amines" by Da-Qing Shi and others, published in the "Journal of Organic Chemistry" in 2015.

Microwave-promoted diethylamine-catalyzed three-component reaction of arylglyoxals, 5-aminopyrazoles, and cyclic 1,3-diones offers a direct synthesis of the title compounds (IV) and (VI) in moderate yields. [ABSTRACT FROM AUTHOR]

An abstract of the article "Cp*Rh(III) and Cp*Ir(III)-Catalyzed Redox-Neutral C--H Arylation with Quinone Diazides: Quick and Facile Synthesis of Arylated Phenols" by S.-S. Zhang and colleagues is presented.

The reaction offers a simple and practical route for the synthesis of allylated arenes and skipped dienes with good stereoselectivity and high yields. [ABSTRACT FROM AUTHOR]

The luminescence and fluorescence quantum yields of the products are investigated. [ABSTRACT FROM AUTHOR]

This unusual reaction is performed in tetrahydrofuran which is split during the reaction in an unprecedented manner under conditions used, leading to the formation of two geminal C-C bonds via C-H and C-O cleavage. [ABSTRACT FROM AUTHOR]