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Primary and secondary benzylic halides efficiently react with silylboronates affording benzylic silanes with moderate to high yields and broad substrate scope. [ABSTRACT FROM AUTHOR]

affording various multi-substituted alkene products under mild reaction conditions [ABSTRACT FROM AUTHOR]

Highly enantioselective cyanation of β-keto esters such as (I), (IV), and (VI) is achieved using hypervalent iodine reagent (II) as electrophilic cyanating reagent and a cinchona alkaloid-based chiral quaternary ammonium salt as catalyst. [ABSTRACT FROM AUTHOR]

Review: 140 refs. [ABSTRACT FROM AUTHOR]

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

A series of 5-arylisoxazole (II) and related pyrazole derivatives (III) are synthesized via ultrasound assisted reactions of 3-aminopropenone (I) with hydroxylamine or hydrazine hydrate, respectively. [ABSTRACT FROM AUTHOR]

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

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.

Reaction of isonitriles with 3-(arylamino)isobenzofuran-1(3H)-ones in the presence of a catalytic amount of an octahydro (R)-binol-derived chiral phosphoric acid affords 3-oxo-2-arylisoindoline-1-carboxamides in high yields with good to high enantioselectivities. [ABSTRACT FROM AUTHOR]

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

Two rings and four bonds are efficiently formed by an facile one‐pot procedure leading to the desired indole derivatives in excellent yields. [ABSTRACT FROM AUTHOR]

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

A Chemical equation is presented for the article "Copper-Catalyzed Cyclization of 3-Acylcoumarin Hydrazone Using Air as the Oxidant: Efficient Synthesis of Pyrazole-Fused Coumarin Derivatives" by H.Y. Wang and colleagues, published in "Journal of Heterocyclic Chemistry" in 2015.

An abstract of the article "Fe-Promoted Oxidative Cyclization of α-Benzoylthioformanilides for the Synthesis of 2-Benzoylbenzothiazoles" by X. Feng and colleagues is presented.

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]

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]

A convenient microwave promoted three‐component domino reaction of β‐ketoamides (I), pentandial (II), and malononitrile (III) is developed to give deca‐ and octahydroisoquinolines (IV) and (VI). [ABSTRACT FROM AUTHOR]

Diagrams of chemical reactions of Pd-Catalyzed coupling of γ-C(sp3)—H bonds acquired through oxalyl amide-protected amino acids along with aryl iodides and heteroaryl is presented.

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]

An approach to achieve the high site selective meta-C-H arylation of β-arylethylamine via palladium norbornene catalysis under assistance of a N,O bidentate directing group is developed. [ABSTRACT FROM AUTHOR]

Some of the compounds show antiproliferative properties against hepatic carcinoma (HepG2) cells in vitro. [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 title compounds are obtained with high regio- and stereoselectivity by three-component domino reaction of glutaraldehyde, malononitrile, and β-ketoamides under microwave irradiation. [ABSTRACT FROM AUTHOR]

A three-component domino reaction is presented which allows the preparation of the heterocyclic scaffolds under transition metal free conditions A). [ABSTRACT FROM AUTHOR]

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]

22 Title compounds of type (III) or (IV) are prepared in relatively short reaction times. [ABSTRACT FROM AUTHOR]

The article presents chemical equations related to the article "Proline-Catalyzed Dehydrogenative Cross-Coupling Reaction Between Chromene and Aldehydes" by J. Qian and others, published in the journal "Synlett " in 2014.

The synthesis of a large variety of the desired heterocyclic structures becomes possible under microwaves with high regio- and chemoselectivity. [ABSTRACT FROM AUTHOR]

The title compounds (III) and (V) are efficiently obtained by cascade reaction of isatins with enaminones. [ABSTRACT FROM AUTHOR]

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

The synthetic method has the advantages of high yields and good functional group tolerance although very unreactive alkanes are applied in the reaction. [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]

The outcome of the reaction is strongly temperature-dependent. [ABSTRACT FROM AUTHOR]