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101.
Tripathi RP Rastogi SK Kundu B Saxena JK Reddy VJ Srivastava S Chandra S Bhaduri AP 《Combinatorial chemistry & high throughput screening》2001,4(3):237-244
A library of 24 glycoconjugates related to glycosylated beta-amino acid derivative (I) was been prepared and screened against DNA topoisomerase-II of the filarial parasite S. cervi. Among these, compound 6 was found to be a potent inhibitor of DNA topoisomerase-II with 95% inhibition at 1.09 microM. Furthermore, compound 6 was at least three times more potent than the lead compound, glycosylated beta-amino acid derivative I. 相似文献
102.
Kalyan Kali Sen Gupta Mrityunjoy Adbikary Subrata Kumar Mandal Shipra Sen Gupta 《Transition Metal Chemistry》1987,12(2):152-155
Summary The oxidation of MeCHO by chromium(VI) has been studied in HClO4 medium over a wide range of experimental conditions and has been found to obey the rate law;v=k[MeCHO][HCrO
4
–
][H+]. The calculated H
and-S
values for the reaction are 30±2kJ mol–1 and 171±7J mol–1deg–1, respectively. The mechanism is discussed in terms of carbon-hydrogen bond cleavage. 相似文献
103.
The reduction of triphenyltin piperidyl dithiocarbamate in acetone has been investigated using d.c. polarography and cyclic
voltammetry. Polarographic reduction yielded four well-defined waves, two of which were diffusion-controlled and two of which
appear to represent adsorption processes. The cyclic voltammetric study yielded results in close agreement with the polarographic
data. Results appear to indicate the release of the dithiocarbamate moiety, followed by reduction to form the triphenyltin
radical, which undergoes dimerization, as well as reduction to the triphenyltin anion. For comparison, the polarographic reduction
of triphenyltinchloride was investigated. A mechanism similar to that proposed by earlier authors for the polarographic behaviour
of tributyltin oxide was found.
For convenience, the more commonly used terminology of piperidyl dithiocarbamate is used throughout the paper, in place of
(piperidine-1-carbodithioato) triphenyltin (IV). 相似文献
104.
Kalyanmoy Jana Somnath Das Tithi Maity Maidul Hossain Subhas Chandra Debnath 《Journal of Coordination Chemistry》2018,71(10):1497-1509
A new Co(II) complex of general formula [Co(L)2] has been synthesized from a NNO tridentate Schiff base ligand, 2-[(piperidin-2-ylmethylimino)-methyl]-phenol (L). The title complex is characterized by elemental, spectroscopic, antibacterial, and single crystal X-ray structural studies. X-Ray crystallography reveals that the complex shows a distorted octahedral geometry around the Co(II) ion. The complex was tested against several bacteria and shows good antibacterial activities against almost all of the bacteria. The interactions of the title complex with calf thymus deoxyribonucleic acid (CT-DNA) have been investigated by electronic absorption and fluorescence spectroscopy, showing that the complex interacts with CT-DNA via partial intercalation. Thermogravimetric analysis (TGA) of the complex has also been reported and the result shows that the complex is thermally stable up to 134 °C. 相似文献
105.
Rukhsana Ilays Kureshy K. Jeya PrathapManish Kumar Prasanta Kumar BeraNoor-ul Hasan Khan Sayed Hasan Razi AbdiHari Chandra Bajaj 《Tetrahedron》2011,67(43):8300-8307
A series of chiral macrocyclic Cr(III) salen complexes 1-8 were synthesized and characterized. These complexes were found to be highly active, regio-, diastereo-, and enantioselective catalysts in aminolytic kinetic resolution (AKR) of racemic trans-epoxides as well as asymmetric ring opening (ARO) of prochiral meso-epoxides with various anilines as nucleophiles at room temperature in 18-24 h. Excellent yields (>99% with respect to the nucleophile) with high enantioselectivity (ee, >99%) of chiral anti-β-amino alcohols was achieved with concomitant recovery of corresponding epoxides in high ee (up to >99%). The complex 1 also catalyzed the ARO of meso-epoxides to provide corresponding syn-β-amino alcohols in high yield (99%) and ee (up to 91%). Due to built-in basic sites in the catalyst, no external base (as an additive) was required to promote AKR and ARO reactions. The catalyst 1 was conveniently recycled several times with retention of its performance. The AKR of trans-stilbene oxide with aniline was successfully demonstrated at relatively higher scale (10 mmol) using the catalyst 1. 相似文献
106.
Two-dimensional surface properties of PEO-PPO-PEO triblock copolymer film (Mol.Wt. 2800) in the absence and presence of Tyr-Phe dipeptide, Val-Tyr-Val tripeptide, sodium dodecylsulfate and stearic acid have been investigated for the first time at the air/water interface using Langmuir film balance technique. It is observed that the above polymer forms fairly stable film at the air/water interface. There are no significant changes observed in the surface pressure-area (π-A) isotherms of polymer in the presence of SDS. However, more expanded film was formed in presence of SDS since the solubility of the polymer is more in SDS and the polymer network is disturbed in presence of SDS, which results in the increase in surface area of the polymer films. In the presence of dipeptide and tripeptide, the surface area of the polymer film decreased with a slight increase in the surface pressure indicating the binding of these peptides to polymer, which enhances the stability of the polymer film. Thermodynamic studies on the change in surface area (ΔA) and excess free energy of mixing (ΔG(mix)(E)) associated with the formation of the mixed film suggest the occurrence of a thermodynamically unstable mixed film. The presence of SDS slightly decreases the formation of mixed film of stearic acid with triblock copolymer and peptides due to the solubilization of these compounds in SDS. However, the hydrophobicity of the polymer films increases in the presence of stearic acid, leading to the increase in surface pressure. The positive deviation of ΔA and the positive ΔG(mix)(E) values show the non-ideality and incompatibility of thermodynamically unstable mixed films. The thermodynamic results suggest that the stability and compatibility of the polymer, peptides and their mixed films with stearic acid in the presence of SDS are decreased, which is in good agreement with the results obtained for other polymeric systems. 相似文献
107.
The enantioselective synthesis of bio-active 5,6-dihydro-α-pyrone, pectinolide A, has been achieved in 10 steps in good overall yield. Of the three stereogenic centres, the C-5/C-6 vic-diol was obtained using diastereo- and enantioselective Brown hydroxyl crotylation, while the C-3′ stereocentre was created by Jacobsen hydrolytic kinetic resolution method. 相似文献
108.
A first example of organo-N-heterocyclic carbene (NHC) catalyzed click-type fast 1,3-dipolar cycloaddition of nitrile oxides with alkynes was developed for the regioselective synthesis of 3,5-di- and 3,4,5-trisubstituted isoxazoles. Triethylamine (Et(3)N) was employed as an effective base to generate both nitrile oxide and the organo-NHC catalyst in situ. This catalytic approach was used to attach a variety of substituents, including other biologically active fragments, onto the isoxazole ring to selectively design multinucleus structures. Further, we have also optimized the conditions for Cu(I)-free Sonogashira cross-coupling to obtain internal alkynes in high yields, which were subsequently used in cycloaddition. A catalytic cycle is proposed and the remarkable regiocontrol in the formation of isoxazoles was ascribed to a beneficial zwitterion intermediate developed by the interaction of the strongly nucleophilic organo-NHC catalyst with alkyne followed by nitrile oxide. 相似文献
109.
Arijit Ghorai Arun Kumar Mandal Susanta Banerjee 《Journal of polymer science. Part A, Polymer chemistry》2020,58(2):263-279
Sulfonated polytriazoles have drawn a great attention as high performance polymers and their good film forming ability. In the present study, a phosphorus containing new diazide monomer namely, bis-[4-(4′-aminophenoxy)phenyl]phenylphosphine was synthesized and accordingly, a series of phosphorus containing sulfonated polytriazoles (PTPBSH-XX) was synthesized by reacting equimolar amount of this diazide monomer (PAZ) in combination with another sulfonated diazide monomer (DSAZ) and a terminal bis-alkyne (BPALK) by the Cu (I) catalyzed azide–alkyne click polymerization. The polymers were characterized by nuclear magnetic resonance (1H, 13C, 31P NMR) and Fourier transform infrared spectroscopic techniques. The sulfonic acid content of the copolymers also determined from the different integral values obtained from the 1H NMR signals. The small-angle X-ray scattering results unfolded the well-separated dispersion of the hydrophilic and hydrophobic domains of the polymers. As a whole, the copolymer membranes displayed sufficient thermal, mechanical, and oxidative stabilities high with high proton conductivity and low water uptake that are essential for proton exchange membrane applications. The copolymers exhibited oxidative stability in the range of 15–24 h and had proton conductivity values were found as high as 38–110 mS cm−1 at 80 °C in completely hydrated condition. Among the all copolytriazoles, PTPBSH-90 (BPALK:DSAZ:PAZ = 100:90:10) having IECW = 2.44 mequiv g−1, showed proton conductivity as high as 119 mS cm−1 at 90 °C with an activation energy of 10.40 kJ mol−1 for the proton conduction. © 2020 Wiley Periodicals, Inc. J. Polym. Sci. 2020 , 58, 263–279 相似文献
110.