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For the first time, a highly enantioselective rhodium-catalyzed arylation of benzoxazinones and quinoxalinones is realized by employing an unsaturated chiral sulfoxide ligand. [ABSTRACT FROM AUTHOR]

Review: [37 refs. [ABSTRACT FROM AUTHOR]

The title reaction provides a new method for the synthesis of α-diaryl acetates such as (III), (V), and (VII) in good yields and with high enantioselectivities. [ABSTRACT FROM AUTHOR]

Various diarylmethanes are conveniently and efficiently obtained. [ABSTRACT FROM AUTHOR]

An abstract of the article "Copper-Catalyzed Aerobic Decarboxylative Sulfonylation of Cinnamic Acids with Sodium Sulfinates: Stereospecific Synthesis of (E)-Alkenyl Sulfones" by Q. Jiang and colleagues is presented.

This is the first asymmetric N-H insertion of α-diazoketones giving α-aminoketones in good yields and with high enantioselectivities. [ABSTRACT FROM AUTHOR]

Chemical formulas showing highly enantioselective S-H bond insertion cooperatively catalyzed by dirhodium complexes and chiral spiro phosphoric acids are presented.

Review: 103 refs. [ABSTRACT FROM AUTHOR]

The cascade cross-coupling of benzamides with toluene derivatives serves for the efficient construction of various 3-hydroxyisoindolin-1-ones. [ABSTRACT FROM AUTHOR]

An abstract of the article "Iron-Facilitated Oxidative Radical Decarboxylative Cross-Coupling Between α-Oxocarboxylic Acids and Acrylic Acids: An An Approach to α,Β-Unsaturated Carbonyls" by Q. Jiang and colleagues is presented.

The article presents chemical equations related to article "Kinetic Resolution of 2-Substituted-2,3-dihydrofurans by a Palladium-Catalyzed Asymmetric Heck Reaction" by H. Li, and others published in "Royal Society of Chemistry Advances" in 2015.

The article presents chemical equations related to the article "Rhodium(I)-Catalyzed Asymmetric Carbene Insertion into B-H Bonds: Highly Enantioselective Access to Functionalized Organoboranes" published in the periodical "Journal of the American Chemical Society" in 2015.

Depending of the electronic and steric properties of the substrates mono- or dialkoxycarbonylation is achieved. [ABSTRACT FROM AUTHOR]

The article presents a chemical reaction of azaindoles by using 1,2-dicholoroethane.

The article presents chemical equations related to the article "Rhodium-Catalyzed Direct ortho C?N Bond Formation of Aromatic Azo Compounds with Azides" by H. Wang and others, published in the periodical "Journal of Organic Chemistry" in 2014.

The article presents chemical equations related to the article "Rhodium-Catalyzed Direct C-H Bond Cyanation of Arenes with Isocyanide" by X. Hong and others, published in the periodical "Journal of Organic Chemistry" in 2014.