A dissymmetric TTF-type electron donor, cyanobenzene-ethylenedithio-tetrathiafulvalene (CNB-EDT-TTF), was obtained in high yield, by a cross-coupling reaction with triethyl phosphite between 2-thioxobenzo[d][1,3]dithiole-5-carbonitrile and 5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-one. This new donor was characterized namely by single crystal X-ray diffraction, cyclic voltammetry, NMR, UV-...

The cobalt-catalyzed carboxylation of propargyl acetates with CO2 (1 atm) is described. The reaction proceeds at room temperature in the presence of Mn powder as a reducing reagent. Various propargyl acetates are converted to the corresponding carboxylic acids in good to high yields.

n-(diphenylphosphino)triethyl- and tributylammonium salts are introduced as easily prepared, cheap and stable ionic liquids that act as the condensing agent and media for the efficient esterification of acids with alcohols and phenols. this class of ionic liquids is immiscible with the ester products and thus allows simple and easy separation of the desired products from the reaction mixture.

The title compound, C(16)H(13)NOS, was prepared by alkyl-ation of 1-(benzothia-zol-2-yl)propan-2-one with propargyl bromide. The asymmetric unit contains two mol-ecules that are crystallographically independent but linked to each other by non-classical C-H⋯O hydrogen bonds, building up a dimeric substructure. The benzothia-zole rings are essentially planar with maximum deviations of 0.005 (1) a...

We report an efficient method to prepare polysubstituted 3-hydroxypyridines from amino acids, propargyl alcohols, and arylboronic acids. The process involves Pd(0)-catalyzed anti-selective arylative cyclizations of N-propargyl-N-tosyl-aminoaldehydes with acids (“anti-Wacker”-type cyclization), oxidation the resulting 5-substituted-3-hydroxy-1,2,3,6-tetrahydropyridines 3-oxo derivatives, elimina...

Quantum-chemical modeling of the mechanism interaction between propargyl chloride and potassium 1,3-propanedithiolate in hydrazine hydrate–KOH system was carried out using combined approach CCSD(T)/6-31+G*//B3LYP/6-311++G**. The elementary stages reaction, possible intermediates transition states are established

Silica sulfuric acid as an efficient and reusable heterogeneous catalyst has been used for the preparation of amidines 2 from formimidate 1 by reaction with aromatic amines at room temperature in good to excellent yields. Imidate was prepared by treatment of equimolar quantities of triethyl orthoformate and diaminomaleonitrile in refluxing dioxane. All the compounds were characterized fully by ...