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21.
From the fruit coats of the medicinal plant Madhuca latifolia were isolated three new compounds, the triterpenoid madhucic acid (=3β‐(octanoyloxy)‐11‐oxoolean‐12‐en‐28‐oic acid; 1 ), the untypical isoflavone madhushazone (=9‐methoxy‐7‐(2,3,6‐trimethoxyphenyl)‐[1,3]dioxolo[4,5‐g][1]benzopyran‐8(8H)‐one; 2 ), and a bis(isoflavone) named madhusalmone (=5,14‐dimethoxy‐3,12‐bis(3,4,5‐trimethoxyphenyl)‐1,6,8,10,15,17‐hexaoxanaphtho[2′,3′: 6,7]cyclodeca[1,2‐b]naphthalene‐4,13(4H,13H)‐dione; 3 ), as well as eight known constituents, and their structures were elucidated by spectral analysis, including 2D‐NMR techniques. 相似文献
22.
The influence of heat transfer on the steady flow of a fourth‐grade fluid between two stationary parallel porous plates is studied. The flow is engendered under the application of a constant pressure gradient. The concept of homotopy analysis method is utilized for the series solution of the governing problem. Numerical solution has been also carried out. In addition, both analytic and numerical solutions are compared. The variations of embedded parameters into the solution are predicted through the graphical representations. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
23.
Rahila Borissova Abderrachman Debouki Tzanko Nikolov 《Fresenius' Journal of Analytical Chemistry》1993,347(1-2):63-66
Summary Titrimetric methods for a fast determination of phosphates and monofluorophosphates in tooth pastes are described. They are based on the precipitation of PO
4
3–
-ions (directly or after the hydrolysis of PO3F2–-ions) as BiPO4 in nitric acid (pH 0.1–0.5). The end-points are detected visually (back EDTA-titration of the non-bonded Bi3+-ions), or potentiometrically (direct titration of phosphates with bismuth by a specially prepared Bi/Bi2O3-electrode). The titrations are performed without separating the precipitate. An ultrasonic field is applied to accelerate the destruction of the dentifrices. 相似文献
24.
Saify ZS Nisa M Azhar KF Azim MK Rasheed H Mushtaq N Arain MA Haider S Khanum M Ahmed W 《Natural product research》2011,25(20):1965-1968
Piperidine derivatives are reported to exhibit a variety of pharmacological activities. In this article, synthesis and aspartic protease inhibitory activity of three nitrophenacyl derivatives of N-methyl-4-hydroxy piperidine are reported. Enzyme assays showed that the attachment of a nitro group in the benzene ring plays an important role in the inhibition of plasmepsin-II of Plasmodium falciparum. The compound 1-methyl-1-(4'-nitrophenacyl)-4-hydroxypiperidinium bromide (3), consisting of a nitro group at the para position, was the most active at the concentration of 1.0?μM. The activity of the compounds was evaluated through the observed orientation and diagrammatic representation of nitrophenacyl derivatives of 4-hydroxy piperidine. 相似文献
25.
Bina Shaheen Siddiqui Kalamkas Zhanarbekovna Butabayeva Sobiya Perwaiz Huma Aslam Bhatti 《Tetrahedron》2010,66(9):1716-376
A new lignan, rayalinol (1) and a new sesquiterpene kairatene (2) were isolated from Eurotia ceratoides (L.) along with four hitherto unreported syringaresinol, dehydrodiconiferyl aldehyde, dihydrodehydrodiconiferyl alcohol, and dehydrodiconiferyl alcohol and two previously reported constituents ferulic acid and β-sitosterol. The structures of the new constituents were elucidated by extensive spectroscopic means and chemical evidences. Rayalinol is a biogenetically interesting compound with a hitherto unreported 9a homolignane skeleton. Its biosynthetic origin is suggested. 相似文献
26.
Rubina Munir Noman Javid Muhammad Zia-ur-Rehman Muhammad Zaheer Rahila Huma Ayesha Roohi Muhammad Makshoof Athar 《Molecules (Basel, Switzerland)》2021,26(16)
In this article, a synthesis of N’-(benzylidene)-2-(6-methyl-1H-pyrazolo[3,4-b]quinolin-1-yl)acetohydrazides and their structural interpretation by NMR experiments is described in an attempt to explain the duplication of some peaks in their 1H- and 13C-NMR spectra. Twenty new 6-methyl-1H-pyrazolo[3,4-b]quinoline substituted N-acylhydrazones 6(a–t) were synthesized from 2-chloro-6-methylquinoline-3-carbaldehyde (1) in four steps. 2-Chloro-6-methylquinoline-3-carbaldehyde (1) afforded 6-methyl-1H-pyrazolo[3,4-b]quinoline (2), which upon N-alkylation yielded 2-(6-methyl-1H-pyrazolo[3,4-b]quinolin-1-yl)acetate (3). The hydrazinolysis of 3 followed by the condensation of resulting 2-(6-methyl-1H-pyrazolo[3,4-b]quinolin-1-yl)acetohydrazide (4) with aromatic aldehydes gave N-acylhydrazones 6(a–t). Structures of the synthesized compounds were established by readily available techniques such as FT-IR, NMR and mass spectral studies. The stereochemical behavior of 6(a–t) was studied in dimethyl sulfoxide-d6 solvent by means of 1H NMR and 13C NMR techniques at room temperature. NMR spectra revealed the presence of N’-(benzylidene)-2-(6-methyl-1H-pyrazolo[3,4-b]quinolin-1-yl)acetohydrazides as a mixture of two conformers, i.e., E(C=N)(N-N) synperiplanar and E(C=N)(N-N) antiperiplanar at room temperature in DMSO-d6. The ratio of both conformers was also calculated and E(C=N) (N-N) syn-periplanar conformer was established to be in higher percentage in equilibrium with the E(C=N) (N-N) anti-periplanar form. 相似文献
27.
28.
In this paper, we introduce and consider a new class of mixed variational inequalities, which is called the general mixed
variational inequality. Using the resolvent operator technique, we establish the equivalence between the general mixed variational
inequalities and the fixed-point problems as well as resolvent equations. We use this alternative equivalent formulation to
suggest and analyze some iterative methods for solving the general mixed variational inequalities. We study the convergence
criteria of the suggested iterative methods under suitable conditions. Using the resolvent operator technique, we also consider
the resolvent dynamical systems associated with the general mixed variational inequalities. We show that the trajectory of
the dynamical system converges globally exponentially to the unique solution of the general mixed variational inequalities.
Our methods of proofs are very simple as compared with others’ techniques. Results proved in this paper may be viewed as a
refinement and important generalizations of the previous known results. 相似文献
29.
Niaz Muhammad Muhammad Nawaz Tahir Shaukat Shujah Abdul Wadood Huma Khan 《Phosphorus, sulfur, and silicon and the related elements》2013,188(11):1067-1073
AbstractDi-n-butyl- (1) and diethyltin(IV) (2) derivatives of 3-methylphenylethanoic acid were synthesized and characterized by elemental analysis, atomic absorption, IR, 1H and 13C NMR spectroscopy and mass spectrometry. The spectroscopic data and single crystal X-ray diffraction studies for complex 2 have confirmed a bidentate coordination mode of the carboxylate ligand and the presence of hexacoordinated tin atoms in the complexes. The complexes were screened for their in vitro antibacterial activity against selected gram positive and gram negative bacterial strains. The anticancer potential was assessed against prostate cancer cell lines. Both complexes have shown higher activities than the ligand acid. Complex 1 with an IC50 value of 4.97?±?0.27?μg/mL was found to be better anti prostate cancer agent than complex 2 (IC50 = 11.26?±?2.18?μg/mL). Molecular docking study has suggested antibacterial action of the complexes in terms of their ability to develop hydrogen bonding and hydrophobic interactions with vital residues of the target proteins like tyrosyl-tRNA synthase from Staphylococcus aureus (gram-positive bacteria) and undecaprenyl diphosphate synthase from Escherichia coli (gram-negative bacteria). 相似文献
30.
New route to ABCD-porphyrins via bilanes 总被引:1,自引:0,他引:1
Dogutan DK Zaidi SH Thamyongkit P Lindsey JS 《The Journal of organic chemistry》2007,72(20):7701-7714
A new strategy for preparing porphyrins that bear up to four different meso-substituents (ABCD-porphyrins) relies on two key reactions. One key reaction entails a directed synthesis of a 1-protected 19-acylbilane by acid-catalyzed condensation at high concentration (0.5 M) of a 1-acyldipyrromethane and a 9-protected dipyrromethane-1-carbinol (derived from a 9-protected 1-acyldipyrromethane). Three protecting groups (X) were examined, including thiocyanato, ethylthio, and bromo, of which bromo proved most effective. The bilanes were obtained in 72-80% yield, fully characterized, and examined by 15N NMR spectroscopy. The second key reaction entails a one-flask transformation of the 1-protected 19-acylbilane under basic, metal-templating conditions to give the corresponding metalloporphyrin. The reaction parameters investigated for cyclization of the bilane include solvent, metal salt, base, concentration, temperature, atmosphere, and time. The best conditions entailed the 1-bromo-19-acylbilane at 100 mM in toluene containing DBU (10 mol equiv) and MgBr2 (3 mol equiv) at 115 degrees C exposed to air for 2 h, which afforded the magnesium porphyrin in 65% yield. The magnesium porphyrin is readily demetalated to give the free base porphyrin. A stepwise procedure (which entailed treatment of the 1-(ethylthio)-19-acylbilane to oxidation, metal complexation, desulfurization, carbonyl reduction, and acid-catalyzed condensation) was developed but was much less efficient than the one-flask process. The new route to ABCD-porphyrins retains the desirable features of the existing "2 + 2" (dipyrromethane + dipyrromethane-1,9-dicarbinol) method, such as absence of scrambling, yet has significant advantages. The advantages include the absence of acid in the porphyrin-forming step, the use of a metal template for cyclization, the ability to carry out the reaction at high concentration, the lack of a quinone oxidant, avoidance of use of dichloromethane, and the increased yield of macrocycle formation to give the target ABCD-metalloporphyrin. 相似文献