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Review: [33 refs. [ABSTRACT FROM AUTHOR]

A cyclization of ortho-halobenzamides and carbon disulfide affords benzisothiazolones via a consecutive process involving S-C and S-N bond formation. [ABSTRACT FROM AUTHOR]

The title compounds are prepared by sequential NHC-amine catalytic one-pot cascade reaction of aromatic aldehydes, trifluoroacetaldehyde ethyl hemiacetal, and enals. [ABSTRACT FROM AUTHOR]

leading to chiral oxazolidines [ABSTRACT FROM AUTHOR]

The sulfa-Michael/aldol cascade reaction of 1,4-dithiane-2,5-diol to 2-NO2-porphyrin is developed providing a new facile approach to tetrahydrothiophene-fused porphyrin. [ABSTRACT FROM AUTHOR]

Monolayer WS2(1-x)Se2x (x = 0.18, 0.3, 0.43) is are prepared by simultaneous sulfurization and selenation of WO3 deposited by CVD with 5% H2/Ar as the carrier gas on a Si/SiO2 (300 nm) substrate in a two-zone heater (830 °C at the WO3 deposition site, 300 °C at the S/Se site, 15 min). [ABSTRACT FROM AUTHOR]

Review: 380 refs. [ABSTRACT FROM AUTHOR]

The title reaction provides multifunctionalized tetrahydrofurans such as (III) and (V) bearing all-carbon quaternary stereocenters in high yields with high relative and absolute stereocontrol. [ABSTRACT FROM AUTHOR]

Both title reactions can be performed on gram-scale. [ABSTRACT FROM AUTHOR]

Optimized reaction conditions render possible the selective C-2 alkylation of indoles. [ABSTRACT FROM AUTHOR]

Chemical equations related to the article "Selective Synthesis of 3-Methylene-2,3-dihydrofurans or 1,2,4-Trisubstituted Furans via Tandem Reactions of Allenic Ketones with α-Chloro β-Keto Esters or Ketones" by Q. Wang and others, published in the journal "Synlett" in 2014 are presented.

The structure of the title compound is determined by Rietveld refinement of powder XRD data (space group P21/b). [ABSTRACT FROM AUTHOR]

The article discusses the one pot synthesis of diarylimidazolium salts from 1H-imidazole.

The article presents chemical structures of fused pyridine derivatives representing efficient Rh/Oxygen2 catalytic system for oxidative carbon-hydrogen activation/annulation.

Under optimized conditions, the title reaction provides a facile access to azaarene-containing hydrazines from easily available starting materials. [ABSTRACT FROM AUTHOR]

Synthesis and biological evaluation of title compounds (IV) as potential plant protecting additives to the herbicide acetochlor are described. [ABSTRACT FROM AUTHOR]

The treatment of 2-arylpyridines, 2-arylquinolines, or 1-phenylpyrazole with chalcones or analogues in AcOH as solvent and an optimized Rh/Ag catalyst affords a range of corresponding addition products (32 examples). [ABSTRACT FROM AUTHOR]

Review: ca. 100 refs. [ABSTRACT FROM AUTHOR]

An abstract of the article "Copper-Catalyzed Decarboxylative Cross-Coupling of Cinnamic Acids and ACCN via Single Electron Transfer" by Bao Gao and colleagues is presented.

The title reaction starts from easily available 2-halobenzamides [e.g. (I)] or 2-halonicotinamides (X) and proceeds probably via aromatic nuleophilic substitution of azide/copper catalyzed reduction/imine formation/cyclization/oxidation sequence. [ABSTRACT FROM AUTHOR]

A wide range of 3,4-disubstituted coumarins are efficiently obtained by exploitation of a thiocarbamate group directed C-H bond activation, an annulation with an alkyne, and a desulfurization. [ABSTRACT FROM AUTHOR]

An efficient and concise method for the preparation of compounds (I) from tabulalin is reported. [ABSTRACT FROM AUTHOR]

Amination is carried out in the presence of air with symmetrical aminals to give the products in moderate yields. [ABSTRACT FROM AUTHOR]

The ratio of the products (III) and (IV) depends on the used aldehyde and the reaction temperature. [ABSTRACT FROM AUTHOR]

The addition reaction with various 2-alkylazaarenes leads to heterocycle-containing dinitrile systems, which are useful building blocks for medicinal compounds. [ABSTRACT FROM AUTHOR]

Sarglaperoxide A (I) demonstrates moderate antibacterial and antiinflammatory activities in vitro. [ABSTRACT FROM AUTHOR]

The article presents chemical equations for the article "Palladium-Catalyzed Hydroaminocarbonylation of Alkenes with Amines Promoted by Weak Acid", by H. Huang and others, published in the journal "Tetrahedron Letters" in 2016.

Crystals of (II) and (III) are characterized by single crystal XRD, IR spectroscopy, UV/VIS diffuse reflectance spectroscopy, second harmonic generation (SHG) measurements, and DFT calculations. [ABSTRACT FROM AUTHOR]

The (E)-selective title reaction of cinnamic acid derivatives or unsaturated ketoacids with dimethyl 2,2′-azobis(2-methylpropionate) is described, and depending on the electronic properties of the substituents β,γ-unsaturated carboxylic esters are formed in low to often high yields. [ABSTRACT FROM AUTHOR]

The tandem oxa-Michael-Michael reaction of 2-nitrovinyl phenols (I) with enal (II) followed by reaction of intermediate chromanes with oxindoles (III) leads to chroman-fused spirooxindoles (IV) with high enantioselectivities and good diastereoselectivities. [ABSTRACT FROM AUTHOR]

The presented approach allows the production of two synthetically important compounds with excellent stereo control in a one-pot operation. [ABSTRACT FROM AUTHOR]

Theoretical results obtained for three Ag2CdGeS4 polytypes (two of space group Pna21, one of Pmn21) show the effects of cation arrangement on the electronic and lattice dynamic properties such as bonding strength, band structure, and IR spectrum. [ABSTRACT FROM AUTHOR]

The first palladium-catalyzed cascade reaction involving the cleavage of four C-H bonds and the formation of two C-C bonds is presented [viz. [ABSTRACT FROM AUTHOR]

Review: 217 refs. [ABSTRACT FROM AUTHOR]