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The [Cu(acac)2]‐catalyzed reactions of α,β‐unsaturated carboxamides with dimethyl diazomalonate yielded dihydrofuran derivatives by a 1,5‐electrocyclic reaction at C(β), and butadiene derivatives by carbene addition reaction at C(α) (Schemes 4 and 5; Table). Phenyl substituents at the N‐atom of the amides seem to be effective on the reaction pathways (Table). 相似文献
3.
A Genetic Algorithm (GA) is an evolutionary computation technique inspired by the principle of biological evolution via natural
selection. It employs the fundamental components of evolution, such as selection, mating, and mutation, which continue from
generation to generation, creating better solutions as time progresses. Although it is mostly used as an optimization tool,
GA enjoys a wide spectrum of applications in diverse fields such as engineering, medicine, and ecology, among others. In this
study, we propose three different population size reduction methods for a typical GA optimization, aiming to increase efficiency.
Additionally, we compare the accuracy and precision of these methods using Monte Carlo simulations. 相似文献
4.
Planar laser induced fluorescence (PLIF) and digital particle image velocimetry (DPIV) combined with Lagrangian coherent structure
(LCS) techniques are utilized to measure ambient fluid entrainment during laminar vortex ring formation and relate it to the
total entrained volume after formation is complete. Vortex rings are generated mechanically with a piston-cylinder mechanism
for a jet Reynolds number of 1,000, stroke ratios of 0.5, 1.0 and 2.0, and three velocity programs (Trapezoidal, triangular
negative and positive sloping velocity programs). The quantitative observations of PLIF agree with both the total ring volume
and entrainment rate measurements obtained from the DPIV/LCS hybrid method for the jet Reynolds number of 1,000, trapezoidal
velocity program and stroke ratio of 2.0 case. In addition to increased entrainment at smaller stroke ratios observed by others,
the PLIF results also show that a velocity program utilizing rapid jet initiation and termination enhances ambient fluid entrainment.
The observed trends in entrainment rate and final entrained fluid fraction are explained in terms of the vortex roll-up process
during vortex ring formation. 相似文献
5.
B. Kahveci M. Özil E. Menteşe O. Bekircan K. Buruk 《Russian Journal of Organic Chemistry》2008,44(12):1816-1820
A number of 3-aryl-4-arylmethylideneamino-4,5-dihydro-1H-1,2,4-triazol-5-ones were synthesized by reaction of the corresponding aromatic aldehydes with 4-amino-3-aryl-1H-1,2,4-triazol-5-ones in anhydrous ethanol under microwave irradiation. The newly synthesized 1H-1,2,4-triazole derivatives were tested for antimicrobial activity. They showed no antibacterial activity but slight mycostatic
activity against some Candida species.
Published in Russian in Zhurnal Organicheskoi Khimii, 2008, Vol. 44, No. 12, pp. 1843–1847.
The text was submitted by the authors in English. 相似文献
6.
Olcay Bekircan Zekeriya Bıyıklıoğlu Irfan Acar Hakan Bektas Halit Kantekin 《Journal of organometallic chemistry》2008,693(21-22):3425-3429
The synthesis of metallophthalocyanines [6–9; M = Ni(II), Zn(II), Co(II) and Cu(II)] with four 1,2,4-triazole units obtained from 4-{(4-chloro-2-fluorobenzyl)[3-(4-chlorophenyl)-5-(4-methylphenyl)-4H-1,2,4-triazol-4-yl]amino}phthalonitrile (5) in the presence of dimethylaminoethanol and the corresponding anhydrous metal salts is described. The thermal stabilities of the Pc compounds were determined by thermogravimetric analysis. The new compounds were characterized by a combination of IR, 1H NMR, 13C NMR, UV–Vis, elemental analysis. 相似文献
7.
Tandem carbonyl ylide formation-1,3-dipolar cycloaddition of α-diazo N-acetyl-tetrahydro-β-carbolin-1-one derivatives occur efficiently in the presence of a dirhodium catalyst to afford bimolecular cycloadducts in high yield. The Rh(II)-catalyzed reaction also takes place intramolecularly to give products derived from trapping of the carbonyl ylide dipole with a tethered alkene. The power of the intramolecular cascade sequence is that it rapidly assembles a pentacyclic ring system containing three new stereocenters and two adjacent quaternary centers stereospecifically in a single step and in high yield. 相似文献
8.
A new borate ion selective electrode using solid salts of Ag3BO3, Ag2S and Cu2S has been developed. Detailed information is provided concerning the composition, working pH and conditioning of the electrode. An analytically useful potential change occurred from 1 × 10−6 to 1 × 10−1 M borate ion. The slope of the linear portion was 31 ± 2 mV/10-fold changes in borate concentration. The measurements were made at constant ionic strength (0.1 M NaNO3) and at room temperature. The effect of Cl−, Br−, NO3−, SO=4, H2PO4− anions and K+, Na+, Cu2+, Ag+, Ca2+ cations on borate response is evaluated and it was found that only Ag+ had a small interference effect. The lifetime of the electrode was more than two years, when used at least 4-5 times a day, and the response time was about 20-30 s. Borate content in waste water of borax factory, tap water of a town situated near to the borax factory and city tap water far from these mines were also determined. The validation was made with differential pulse polarography for the same water sample, and high consistency was obtained. 相似文献
9.
The molecular structures and vibrational spectra of the three isomers of pyridinecarboxamide (picolinamide, nicotinamide, isonicotinamide) were calculated with the Density Functional Theory (DFT) method using the B3LYP function and the 6-31++G(d,p), Z2PolX, Z3PolX basis sets. The calculations were performed by using the Gaussian98W packet program set. The total energy distributions (TED) of the vibrational modes of these molecules were calculated by using the Scale 2.0 program and the vibrational modes of the molecules were determined. The Scaled Quantum Mechanical (SQM) method was used in the scaling procedure. In the experimental part of the study, the solid phase FT-IR and Micro Raman spectra of the three isomers of pyridinecarboxamide have been recorded in the range of 4000-650 and 1200-100 cm−1, respectively. The calculated wavenumbers were compared to the corresponding experimental values. As a result, the observed bands of the three isomers of pyridinecarboxamide were assigned with good accuracy. 相似文献
10.
First ever non-deformylating transdiazotization of acylacetaldehydes was achieved: the reactions of 2-azido-l-ethylpyridinium tetrafluoroborate ( 4 ) with acylacetaldehydes 3 proceeded partially without deformylation to yield 16 new α-diazo-β-oxoaldehydes 1 along with diazomethyl ketones 2 , especially in the presence of NaOAc (Scheme 1, Tables 1 and 2). The product distribution was substituent-dependent and could be correlated quantitatively. This new diazotization reaction appears as an alternative, direct, and more general method for the synthesis of these diazooxoaldehydes. α-Oxocycloalkanecarbaldehydes 5 gave only traces (if any) of α-diazocycloalkanones 7 , and rearrangement products 6 were isolated (Scheme 2). Mechanisms of the reactions are discussed (Schemes 4 and 5). 相似文献