Microwave-assisted unimolecular isomerization-Claisen domino reactions of 1,3-di(hetero)aryl propargyl trityl ethers lead, depending on the basicity of the amine, either to the formation of tricyclo[3.2.1.0(2,7)]oct-3-enes (with triethylamine) or to indanes (with DBU). Based upon product analyses and computations, this base dependent dichotomy can be rationalized as a sequel of pericyclic react...

The aim of this study was to synthesize novel ionic compound – 1-propargyl-1-(2-methyl-3-oxo-3-(p-tolyl)propyl)-piperidin-1-ium bromide via the N-alkylation (in conventional conditions and using ultrasound activation), investigate its influence on plant growth-stimulating activity sweet sorghum seeds. synthesized fully characterized by infrared (IR) nuclear magnetic resonance (NMR) spectroscopy...

4-amino-6-methyl- 1,2,4-triazine-3(2h)-thione-5-0ne (1) was condensed with propargyl bromidein the presence of sodium rnethoxide to afford 3-propargylmercapto- 4-arnino-6-rnethyl-1,2,4-triazin-5-one(2) . transformation of the latter to 8-dihydro- 3-methyl-7-methylene-4-oxo-6h-[1,2,4]triazino [3,4-b] [1,3,4] thiadiazine (3) was performed under the condition of palladium (ii) salt. ring closure o...

First-row metal complexes often undergo undesirable one-electron redox processes during two-electron steps of catalytic cycles. We report the amination of aryl chlorides and bromides with primary aliphatic amines catalyzed by a well-defined, single-component nickel precursor (BINAP)Ni(η(2)-NC-Ph) (BINAP = 2,2'-bis(biphenylphosphino)-1,1'-binaphthalene) that minimizes the formation of Ni(I) spec...

This paper examines the unimolecular dissociation of propargyl (HCCCH2) radicals over a range of internal energies to probe the CH+HCCH and C+C2H3 bimolecular reactions from the radical intermediate to products. The propargyl radical was produced by 157 nm photolysis of propargyl chloride in crossed laser-molecular beam scattering experiments. The H-loss and H2 elimination channels of the nasce...

Two ionic liquids triethylammonium oleate and stearate were synthesized from fatty acids triethyl amine using two different methods (one step three methods). The yield rearch 68.8-74% method) 86.3% (three of 68.7-74.1 83.5% method). one method spends more time but less chemicals brings higher yield. FT-IR 1H-NMR spectra ILs obtained both was measured. results showed that synthesis doesn’t affec...

The reaction between benzyl-triethyl-ammonium chloride and dimethyl-tin dichloride yields the title salt, [(C(6)H(5)CH(2))(C(2)H(5))(3)N](2)[SnCl(6)]. The Sn(IV) atom, located on a center of inversion, exists in an octa-hedral coordination environment. The cation links with the anion via weak C-H⋯Cl hydrogen bonding.