A novel methodology has been devised for the chemoselective reduction of enones involving the use of nBu3SnH and azobisisobutyronitrile. The 1,4-reduction of variously substituted α,β-unsaturated cyclic and acyclic enones has been successfully carried out under free radical reaction conditions. The reaction has been determined to proceed via single-electron transfer.
[Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications® for the following free supplemental resource(s): Full experimental and spectral details.] 相似文献
Cyclization of enantiopure (S/R)-1 with halogen-reagent-constructed enantiopure octahydrobenzofuran core structure with contiguous three stereogenic centers of both enantiomers (SRR and RSS). The absolute configurations of all compounds have been established from x-ray analysis of the single crystal of (3aS,7aR,7R)-3. The chiral initiation in diastereoselective mode of 5-exo ring closure across C?C bond of pendant cyclohexene moiety has been proposed. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications® for the following free supplemental resource(s): Full experimental and spectral details.] 相似文献
The Suzuki–Miyaura coupling reaction was applied for the synthesis of biologically relevant derivatives of known mucolytic agents Bromhexine and Ambroxol. Using commercially available electron-rich and electron-poor arylboronic acids the desired products are obtained in moderate to high yields (42–81%). 相似文献
The synthesis of novel CO2 philic surfactant using maleic anhydride and dipropylene tertiary butyl alcohol is reported. The synthesis involved the esterification of maleic anhydride to produce bis(2-(2-(tert-butoxy)propoxy)propyl) maleate and subsequent sulfonation of the esterified product. Para toluene sulfonic acid was employed as catalyst for the esterification reaction. The esterification reaction was optimized for the maximum yield of 98% of bis(2-(2-(tert-butoxy)propoxy)propyl) maleate. The esterification reaction kinetics employing heterogeneous catalyst were also studied. Although this is a bimolecular reaction, a first order reaction kinetics with respect to acid has been observed. The activation energy was found to be 58.71 kJ/mol. The diester was followed by the sulfonation process and a yield of 85% of surfactant was achieved. The synthesized surfactant successfully lowered down the IFT between CO2/brine to 1.93 mN/m. This surfactant has a great potential to be used for CO2-EOR applications. 相似文献
Positive and negative streamer discharges in atmospheric pressure air were generated in a shielded sliding discharge reactor at operating voltages as low as 5 kV for a gap length of 1.6 cm. In this reactor, electrodes are placed on top of a dielectric layer and one of the electrodes, generally the one on ground potential, is connected to a conductive layer on the opposite side of the dielectric. The energy per pulse, at the same applied voltage, was more than a factor of seven higher than that of pulsed corona discharges, and more than a factor of two higher than that of sliding discharges without a shield. It is explained on the basis of enhanced electric fields, particularly at the plasma emitting electrode. Specific input energy required for 50 % removal from ~1,000 ppm initial NO could be reduced to ~18 eV/molecule when ozone in the exhaust of negative streamers was utilized. For sliding discharges and pulsed corona discharges this value was ~25 eV/molecule and it was 35 eV/molecule for positive shielded sliding discharges. Also, the ozone energy yield from dry air was up to ~130 g/kW h and highest for negative streamer discharges in shielded sliding discharge reactors. The high energy density in negative streamer discharges in the shielded discharge reactor at the relatively low applied voltages might not only allow expansion of basic studies on negative streamers, but also open the path to industrial applications, which have so far been focused on positive streamer discharges. 相似文献
This Letter reveals a unique, user-friendly, concise two-step, one-pot protocol for the synthesis of highly substituted quinoxalines. Conducting the Ugi reaction with appropriately functionalized classical Ugi reagents with subsequent acid treatment of the Ugi adduct affords collections of diversified quinoxalines in good to excellent yields. The methodology exploits what may be viewed as a ‘convertible carboxylic acid’, which in addition may be captured in an intramolecular sense to generate structurally complex 2-benzimidazolylquinoxalines in a mere two steps. 相似文献
The independent isomeric yield ratios of 95m,gNb from the natMo(γ, pxn) reactions with bremsstrahlung end-point energies of 45, 50, 55, 60, and 70 MeV were determined by an activation and an off-line γ-ray spectrometric technique at the Pohang accelerator laboratory (PAL), Korea. The isomeric yield ratios of 95m,gNb from the natZr(p, xn) reactions were also determined in eight different proton energies within 19.4–44.7 MeV by a stacked-foil activation and an off-line γ-ray spectrometric technique using the MC-50 cyclotron of Korea Institute of Radiological and Medical Sciences (KIRAMS), Korea. The measured isomeric yield ratios of 95m,gNb from the present work and the literature data in the natMo(γ, pxn) and natZr(p, xn) reactions were compared with the similar literature data in the natMo(p, αxn) reactions. It was found that the isomeric yield ratio of 95m,gNb increases with projectile energy, which indicate the effect of excitation energy. However, at the same excitation energy, the isomeric yield ratios of 95m,gNb in the natZr(p, xn) and natMo(p, αxn) reactions are higher than those in the natMo(γ, pxn) reaction, which indicates the role of input angular momentum. The isomeric yield ratios of 95m,gNb in the natMo(γ, pxn), natZr(p, xn), and natMo(p, αxn) reactions were also calculated using computer code TALYS 1.4. The calculated isomeric yield ratios of 95m,gNb from three reactions increase with excitation energy. However, in all the three reactions, the calculated values are significantly higher than the experimental data. 相似文献
In contrast to the approach of coupling a nonlinear oscillator that represents the lift force with the cylinder’s equation of motion to predict the amplitude of vortex-induced vibrations, we propose and show that the displacement can be directly predicted by a nonlinear oscillator without a need for a force model. The advantages of the latter approach include reducing the number of equations and, subsequently, the number of coefficients to be identified to predict displacements associated with vortex-induced vibrations. The implemented single-equation model is based on phenomenological representation of different components of the transverse force as required to initiate the vibrations and to limit their amplitude. Three different representations for specific flow and cylinder parameters yielding synchronization for Reynolds numbers between 104 and 114 are considered. The method of multiple scales is combined with data from direct numerical simulations to identify the parameters of the proposed models. The variations in these parameters with the Reynolds number, reduced velocity or force coefficient over the synchronization regime are determined. The predicted steady-state amplitudes are validated against those obtained from high-fidelity numerical simulations. The capability of the proposed models in assessing the performance of linear feedback control strategy in reducing the vibrations amplitude is validated with performance as determined from numerical simulations.
Reactive dyes are vastly used in dyeing and printing of cotton fibre. These dyes have a distinctive reactive nature due to active groups which form covalent bonds with -OH groups of cotton through substitution and/or addition mechanism. Among many methods used for dyeing cotton with reactive dyes, the Cold Pad Batch (CPB) method is relatively more environment friendly due to high dye fixation and non requirement of thermal energy. The dyed fabric production rate is low due to requirement of at least twelve hours batching time for dye fixation. The proposed CPB method for dyeing cotton involves ultrasonic energy resulting into a one third decrease in batching time. The dyeing of cotton fibre was carried out with CI reactive red 195 and CI reactive black 5 by conventional and ultrasonic (US) method. The study showed that the use of ultrasonic energy not only shortens the batching time but the alkalis concentrations can considerably be reduced. In this case, the colour strength (K/S) and dye fixation (%F) also enhances without any adverse effect on colour fastness of the dyed fabric. The appearance of dyed fibre surface using scanning electron microscope (SEM) showed relative straightening of fibre convolutions and significant swelling of the fibre upon ultrasonic application. The total colour difference values ΔE (CMC) for the proposed method, were found within close proximity to the conventionally dyed sample. 相似文献