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Статті в журналах з теми "Pure compounds"

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Автор: Grafiati

Опубліковано: 8 червня 2024

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1

Babalola, F. U., and A. A. Susu. "Stability Limit Determination for Pure Compounds." Petroleum Science and Technology 26, no. 12 (July 21, 2008): 1481–97. http://dx.doi.org/10.1080/15567030701776783.

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2

Linde, Bogumił B. J., and Nikołaj B. Lezhnev. "Ultrasonic spectroscopy of pure cyclic compounds." Ultrasonics 44 (December 2006): e1467-e1470. http://dx.doi.org/10.1016/j.ultras.2006.05.146.

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3

López Cortés, José Guadalupe, Sandrine Vincendeau, Jean-Claude Daran, Eric Manoury, and Maryse Gouygou. "Three new enantiomerically pure ferrocenylphosphole compounds." Acta Crystallographica Section C Crystal Structure Communications 62, no. 5 (April 13, 2006): m188—m191. http://dx.doi.org/10.1107/s0108270106010833.

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4

Kitazume, Tomoya, and Jenq Tain Lin. "Synthetic approach to optically pure trifluoromethylated compounds." Journal of Fluorine Chemistry 34, no. 3-4 (January 1987): 461–70. http://dx.doi.org/10.1016/s0022-1139(00)85187-8.

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5

Overdevest, Pieter E. M., and Albert van der Padt. "ChemInform Abstract: Optically Pure Compounds from Ultrafiltration." ChemInform 31, no. 7 (June 10, 2010): no. http://dx.doi.org/10.1002/chin.200007285.

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6

Buendia, Julien, Jakob Mottweiler, and Carsten Bolm. "Preparation of Diastereomerically Pure Dilignol Model Compounds." Chemistry - A European Journal 17, no. 49 (November 10, 2011): 13877–82. http://dx.doi.org/10.1002/chem.201101579.

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7

PYNE, S. G. "ChemInform Abstract: Synthesis of Enantiomerically Pure Compounds." ChemInform 23, no. 11 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199211295.

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8

Bauer, Sebastian, Steffen Tschirschwitz, Peter Lönnecke, René Frank, Barbara Kirchner, Matthew L. Clarke, and Evamarie Hey-Hawkins. "Enantiomerically Pure Bis(phosphanyl)carbaborane(12) Compounds." European Journal of Inorganic Chemistry 2009, no. 19 (July 2009): 2776–88. http://dx.doi.org/10.1002/ejic.200900304.

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9

Gharagheizi, Farhad. "Prediction of the Standard Enthalpy of Formation of Pure Compounds Using Molecular Structure." Australian Journal of Chemistry 62, no. 4 (2009): 376. http://dx.doi.org/10.1071/ch08522.

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A predictive approach has been presented to calculate the standard enthalpy of formation of pure compounds based on a quantitative structure–property relationship technique. A large number (1692) of pure compounds were used in this study. A genetic algorithm based on multivariate linear regression was used to subset variable selection. Using the selected molecular descriptors an optimized feed forward neural network was presented to predict the ΔHfo of pure compounds.

10

Vulić, Predrag, Volker Kahlenberg, Christian Gspan, and Radovan Dimitrijević. "Reinvestigation of pure Na-nepheline like compounds obtained from the thermal conversion of zeolite LTA." European Journal of Mineralogy 25, no. 3 (September 13, 2013): 473–78. http://dx.doi.org/10.1127/0935-1221/2013/0025-2293.

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11

Schwab, R. G., T. Pimpl, H. Schukow, A. Stolle, and D. K. Breitinger. "Compounds of the crandallite-type: Synthesis, properties and thermodynamic data of pure crandallite and woodhouseite." Neues Jahrbuch für Mineralogie - Monatshefte 2004, no. 9 (August 20, 2004): 385–409. http://dx.doi.org/10.1127/0028-3649/2004/2004-0385.

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12

Dorenbos, Pieter. "Electronic Structure of Bi-Activated Luminescent Compounds and Pure Bismuth Photocatalytic Compounds." ECS Journal of Solid State Science and Technology 10, no. 8 (August 1, 2021): 086002. http://dx.doi.org/10.1149/2162-8777/ac19c6.

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13

Shinta, Dewi Yudiana, Yusmarini Yusmarini, Herix Sonata MS, Hilwan Yuda Teruna, and Saryono Saryono. "Uji Bioaktivitas Antibakteri Senyawa murni dari Jamur Endofit Sporothrix sp Terhadap Bakteri Escherichia coli dan Staphylococcus aureus." Dinamika Lingkungan Indonesia 6, no. 1 (January 9, 2019): 37. http://dx.doi.org/10.31258/dli.6.1.p.37-44.

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Modern medicines that are developing now come from active ingredients isolated from plants that require large amounts of plants. The development of new drugs from endophytic fungi found obstacles in the amount of pure compounds produced. Therefore further research is needed by using endophytic fungi as a new antimicrobial producer. This study aims to see the ability or activity of pure compounds produced by Sporothrix sp endophytic fungi from Dahlia tuber (Dahlia variabilis). Test the activity of pure compounds produced by Sporothrix sp. Endophytic fungi on E. coli and Staphylococcus aureus determined by disc diffusion method. With doses of 10, 30 and 50μg/disk. In Escherichia coli bacteria doses 10 and 50μg/disk gave significant inhibition of pure compounds from isolation compared to the positive control of ciprofloxacin, which was marked by a statistically significant test result (p <0.05). In contrast to Staphylococcus aureus there was no significant difference in doses of both doses of 10.30 and 50μg/disk. Determination of pure compounds was carried out by HPLC and Infra Red Spectrophotometry.

14

MOTOI, Tetsuya, Kiyoshi FUKUOKA, and Hideo YOSHIDA. "Nodularization of .ALPHA.-AlFeSi compounds in pure aluminum." Journal of Japan Institute of Light Metals 48, no. 12 (1998): 624–28. http://dx.doi.org/10.2464/jilm.48.624.

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15

Srikanth, G., Uttam Kumar Ray, D. V. N. Srinivas Rao, P. Badarinadh Gupta, P. Lavanya, and Aminul Islam. "Efficient Approach to Pure Entacapone and Related Compounds." Synthetic Communications 42, no. 9 (January 11, 2012): 1359–66. http://dx.doi.org/10.1080/00397911.2010.539894.

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16

Jacobson, Nathan. "Use of Tabulated Thermochemical Data for Pure Compounds." Journal of Chemical Education 78, no. 6 (June 2001): 814. http://dx.doi.org/10.1021/ed078p814.

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17

Bravo, P., G. Resnati, and C. Zappalà. "Synthesis of enantiomerically pure, nitrogen substituted fluoroorganic compounds." Journal of Fluorine Chemistry 54, no. 1-3 (September 1991): 287. http://dx.doi.org/10.1016/s0022-1139(00)83796-3.

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18

Li, Y. C., C. P. Wang, and X. J. Liu. "Calculation of Thermodynamic Properties in Pure Organic Compounds." Journal of Phase Equilibria and Diffusion 30, no. 1 (December 17, 2008): 46–58. http://dx.doi.org/10.1007/s11669-008-9425-6.

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19

Gurjar, M. K. "Synthesis of enantiomerically pure compounds of biological interest." Pure and Applied Chemistry 62, no. 7 (January 1, 1990): 1293–98. http://dx.doi.org/10.1351/pac199062071293.

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20

Vogt, O. "Properties of pure single crystals of actinide compounds." Journal of Nuclear Materials 166, no. 1-2 (July 1989): 36–40. http://dx.doi.org/10.1016/0022-3115(89)90172-4.

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21

Wei, Fuxiang, and L. Fang. "Pure-blue tandem OLEDs based on terfluorenes compounds." Journal of Materials Science: Materials in Electronics 19, no. 12 (December 29, 2007): 1202–5. http://dx.doi.org/10.1007/s10854-007-9528-6.

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22

Bhagwat, Sunil S., Ashwin Kane, Sparsh Ganju, and Prafullachandra P. Vora. "Simple correlation for critical isotherm of pure compounds." Chemical Engineering Science 192 (December 2018): 1036–40. http://dx.doi.org/10.1016/j.ces.2018.08.043.

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23

Albahri, Tareq A., and Dalal A. Alashwak. "Modeling of pure compounds surface tension using QSPR." Fluid Phase Equilibria 355 (October 2013): 87–91. http://dx.doi.org/10.1016/j.fluid.2013.06.052.

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24

Michotte, D., H. Rogez, R. Chirinos, E. Mignolet, D. Campos, and Y. Larondelle. "Linseed oil stabilisation with pure natural phenolic compounds." Food Chemistry 129, no. 3 (December 2011): 1228–31. http://dx.doi.org/10.1016/j.foodchem.2011.05.108.

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25

Watts, P., and C. Wiles. "Synthesis of Analytically Pure Compounds in Flow Reactors." Chemical Engineering & Technology 30, no. 3 (March 2007): 329–33. http://dx.doi.org/10.1002/ceat.200600323.

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26

M, Alhasno. "Studying the Structural Properties of Compounds Fluoride that Blotched by Sb." Physical Science & Biophysics Journal 6, no. 2 (October 12, 2022): 1–5. http://dx.doi.org/10.23880/psbj-16000224.

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Анотація:

Sb doped calcium fluoride transparent conducting powder were prepared by solid state reaction method. Structural properties of the samples were investigated as a function of various Sb-doping levels (x=0.00-0.04-0.05-0.06). The results of x-ray diffraction have shown that the samples are polycrystalline structure in cubic phase and show presence (111) ،(220) ،(311) ،(400) planes in pure CaF2 sample and The preferred orientation is (220) for pure CaF2 and we have peaks correspond to (012), (015), (024), (122) for Sb for all samples and the preferred orientation is (015) for Sb for all samples. The average of crystallite size is within the range [4.063-0.915 nm] for all samples. The relative intensities, distance between crystalline planes (d), crystallite size (D) and lattice parameters (a) were determined.

27

Takahashi, Toshihiro, Takashi Mizuno, Tatsuo Ido, Ren Iwata, and Ken-ichi Watanabe. "Improved synthesis of pure [18F]fluoro-compounds for PET studies from bromo-compounds." Applied Radiation and Isotopes 58, no. 5 (May 2003): 557–66. http://dx.doi.org/10.1016/s0969-8043(03)00053-8.

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28

Yang, Yan, Fengyun Wang, Fernande D. Rochon та Margaret M. Kayser. "Synthesis of novel optically pure β-lactams". Canadian Journal of Chemistry 83, № 1 (1 січня 2005): 28–36. http://dx.doi.org/10.1139/v04-159.

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Several new β-lactams were synthesized as racemates via a Staudinger reaction. The corresponding optically pure compounds were obtained in subsequent biotransformation steps either through baker's yeast reduction or lipase resolution. Their absolute configurations were established. The X-ray crystal structures of three new substituted β-lactams are reported here. These compounds represent key building blocks for a variety of medicinally important molecules, including inhibitors of aspartyl proteases and Taxol® analogues.Key words: optically pure β-lactams, lipase resolutions, baker's yeast reductions, Staudinger reaction.

29

Aisyah, Lilis Siti, Delia Ilfani, Faridia Puspita Lestari та Yenny Febriani Yun. "α-Amylase Inhibition Activities by Flavonoid Compounds from Panda Plants (Kalanchoe tomentosa)". Jurnal Kimia Sains dan Aplikasi 23, № 3 (11 березня 2020): 96–101. http://dx.doi.org/10.14710/jksa.23.3.96-101.

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Diabetes mellitus (DM) is one of the major health problems. One way to deal with diabetes mellitus is by inhibiting the work of enzymes that hydrolyze carbohydrates, thereby reducing glucose absorption. The enzyme that plays a role in the breakdown of starch into simple sugars is the α-amylase. The genus Kalanchoe or Panda plant has been widely reported to contain a variety of secondary metabolites that have several activities such as antimalarial, antibacterial, antidiabetic, and anticancer potential. This study aims to isolate, determine the chemical structure, and test the inhibitory activity of α-amylase from the ethyl acetate fraction of K. tomentosa leaves. The isolation stage began with the maceration process with n-hexane and fractionated with ethyl acetate. Ethyl acetate extract was refracted using a gradient liquid vacuum chromatography (KCV) method (n-hexane: ethyl acetate: methanol). Repeated gravity columns separated the fraction of KCV results and preparative thin-layer chromatography (TLC-P) to obtain isolate pure. Isolate pure was characterized using several spectroscopic methods, including UV-Vis, IR, NMR. Determination of the structure of the compound against isolate pure shows that this isolate is a 3,7,4’-trihydroxyflavonol or kaempferol compound. The results of the test activity of 3,7,4’-trihydroxyflavonol compounds in inhibiting the enzyme α-amylase in vitro showed an IC50 value of 346 µU/mL. The results obtained indicate that the IC50 value is higher than that of the Acarbose, which was 39.3 µU/mL.

30

Wu, Zhi-Ping, Gui-Jun Liu, Cai-Cai Zhu, Zhi-Mei Li, Xi-Cun Gao, and Qian-Yong Cao. "Violet-blue- or pure-blue-emitting triphenylamine derivatives: synthesis and properties." Canadian Journal of Chemistry 91, no. 11 (November 2013): 1043–47. http://dx.doi.org/10.1139/cjc-2012-0473.

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We report the synthesis and optoelectronic properties of a series of nine triphenylamine derivatives. They were synthesized by Suzuki cross-coupling reactions and characterized by elemental analysis, nuclear magnetic resonance, ultraviolet visible absorption spectra, fluorescence spectra, and cyclic voltammetry. All compounds exhibit reversibly electrochemical behavior. In solid state, compounds 5 and 9 emit near violet blue and compounds 1, 2, 4, 6, 7, and 8 emit deep blue or pure blue and compound 3 emits green. Of all of these compounds, compounds 1, 3, 4, and 8 exhibit high fluorescence quantum yields (44%–68%) with the best coplanarity. Compared with them, compounds 5 and 9 have the lowest fluorescence quantum yields due to the least coplanarity. With the similarity in structure with those reported in literature, these compounds can be potentially useful for blue-emitting, host, and up-converting materials.

31

Jiménez-Arellanes, Adelina, Rosalba León-Díaz, Mariana Meckes, Amparo Tapia, Gloria María Molina-Salinas, Julieta Luna-Herrera, and Lilián Yépez-Mulia. "Antiprotozoal and Antimycobacterial Activities of Pure Compounds fromAristolochia elegansRhizomes." Evidence-Based Complementary and Alternative Medicine 2012 (2012): 1–7. http://dx.doi.org/10.1155/2012/593403.

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We analyzed the antimycobacterial activity of the hexane extract of rhizomes fromAristolochia elegans. Some compounds of this extract were purified and tested against a group of drug-resistantMycobacterium tuberculosisstrains. We also evaluated their antiprotozoal activities. The hexane extract was active againstM. tuberculosisH37Rv at aMIC=100 μg mL−1; the pure compounds eupomatenoid-1, fargesin, and (8R,8′R,9R)-cubebin were active againstM. tuberculosisH37Rv (MIC = 50 μg mL−1), while fargesin presented activity against three monoresistant strains ofM. tuberculosisH37Rv and a MDR clinical isolate ofM. tuberculosis(MIC<50 μg mL-1). Both the extract and eupomatenoid-1 were very active againstE. histolyticaandG. lamblia(IC50<0.624 μg mL-1); in contrast, fargesin and (8R,8′R,9R)-cubebin were moderately active (IC50<275 μg mL-1). In this context, two compounds responsible for the antimycobacterial presented byA. elegansare fargesin and cubebin, although others may exert this activity also. In addition to the antimycobacterial activity, the hexane extract has important activity againstE. histolyticaandG. lamblia, and eupomatenoid-1 is one of the compounds responsible for the antiparasite activity.

32

Saini, Pooja, Ekta Menghani, and Rekha Mithal. "Isolation and Identification of Pure Bioactive Compounds from Cuscuta reflexa Grown on Nerium oleander Host Plant by Flash Column Chromatography and GC-MS/MS Analysis." Asian Journal of Chemistry 32, no. 10 (2020): 2486–88. http://dx.doi.org/10.14233/ajchem.2020.22664.

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In this work, an ethyl acetate extract of Cuscuta reflexa grown on Nerium oleander host plant was used for the isolation and identification of pure bioactive compounds. Chloroform:methanol was used as mobile phase for flash column chromatography. Five pure bioactive compounds were isolated and two compounds were identified using GC-MS/MS technique. Glycerol-1-palmitate and squalene were identified in Cuscuta reflexa using NIST library on the basis of area percentage.

33

Paterson, R. RussellM, and Nelson Lima. "Biomedical effects of mushrooms with emphasis on pure compounds." Biomedical Journal 37, no. 6 (2014): 357. http://dx.doi.org/10.4103/2319-4170.143502.

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34

ISHIHARA, Yoshimi, Jiro TAKANO, Takashi YASUOKA, and Shunmei MITSUZAWA. "The Solubilities of Aromatic Nitro Compounds in Pure Water." NIPPON KAGAKU KAISHI, no. 11 (1996): 987–90. http://dx.doi.org/10.1246/nikkashi.1996.987.

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35

PROST, CAROLE, SOPHIE LE GUEN, PHILIPPE COURCOUX, and MICHEL DEMAIMAY. "SIMILARITIES AMONG 40 PURE ODORANT COMPOUNDS EVALUATED BY CONSUMERS." Journal of Sensory Studies 16, no. 6 (December 2001): 551–65. http://dx.doi.org/10.1111/j.1745-459x.2001.tb00320.x.

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36

Bert, F., P. Mendels, D. Bono, A. Olariu, F. Ladieu, J. C. Trombe, F. Duc, C. Baines, A. Amato, and A. Hillier. "Dynamics in pure and substituted volborthite kagome-like compounds." Physica B: Condensed Matter 374-375 (March 2006): 134–37. http://dx.doi.org/10.1016/j.physb.2005.11.034.

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37

Bachki, Abderrazak, Larry R. Falvello, Francisco Foubelo та Miguel Yus. "Enantiomerically pure γ-oxidofunctionalised organolithium compounds from chiral oxetanes". Tetrahedron: Asymmetry 8, № 15 (серпень 1997): 2633–43. http://dx.doi.org/10.1016/s0957-4166(97)00274-7.

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38

Anakkar, A., N. Isaert, J. M. Buisine, and H. T. Nguyen. "Under pressure studies of TGBAand TGBCphases on pure compounds." Ferroelectrics 212, no. 1 (May 1998): 231–38. http://dx.doi.org/10.1080/00150199808217370.

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39

Adekunle, O. K., Ruchi Acharya, and Bikram Singh. "Toxicity of pure compounds isolated fromTagetes minutaoil toMeloidogyne incognita." Australasian Plant Disease Notes 2, no. 1 (2007): 101. http://dx.doi.org/10.1071/dn07042.

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40

Ader, U., P. Andersch, M. Berger, U. Goergens, R. Seemayer, and M. Schneider. "Hydrolases in organic synthesis: Preparation of enantiomerically pure compounds." Pure and Applied Chemistry 64, no. 8 (January 1, 1992): 1165–70. http://dx.doi.org/10.1351/pac199264081165.

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41

Kramp, Peter, G�nter Helmchen, and Andrew B. Holmes. "Syntheses of enantiomerically pure ent-multifidene and related compounds." Journal of the Chemical Society, Chemical Communications, no. 6 (1993): 551. http://dx.doi.org/10.1039/c39930000551.

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42

Sugiya, Masashi, and Hiroyuki Nohira. "Synthesis of Optically Pure Bisphosphine Oxides and Related Compounds." Bulletin of the Chemical Society of Japan 73, no. 3 (March 2000): 705–12. http://dx.doi.org/10.1246/bcsj.73.705.

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43

Xue, He, Jun-xu Liu, Tong-yan Xia, and Quan-xin Li. "Catalytic Transformation of Oxygenated Organic Compounds into Pure Hydrogen." Chinese Journal of Chemical Physics 29, no. 4 (August 27, 2016): 481–88. http://dx.doi.org/10.1063/1674-0068/29/cjcp1601010.

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44

Jovanović, Jovan D., and Dušan K. Grozdanić. "A correlation for heat of vaporization of pure compounds." Korean Journal of Chemical Engineering 25, no. 6 (November 2008): 1499–508. http://dx.doi.org/10.1007/s11814-008-0247-3.

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45

GRABULOSA, A., J. GRANELL, and G. MULLER. "Preparation of optically pure P-stereogenic trivalent phosphorus compounds." Coordination Chemistry Reviews 251, no. 1-2 (January 2007): 25–90. http://dx.doi.org/10.1016/j.ccr.2006.05.009.

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46

Rowley, Jeffrey R., Richard L. Rowley, and W. Vincent Wilding. "Prediction of pure-component flash points for organic compounds." Fire and Materials 35, no. 6 (November 4, 2010): 343–51. http://dx.doi.org/10.1002/fam.1057.

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47

FERRIER, R. J., R. BLATTNER, K. CLINCH, R. H. FURNEAUX, J. M. GARDINER, P. C. TYLER, R. H. WIGHTMAN, and N. R. WILLIAMS. "ChemInform Abstract: Synthesis of Enantiomerically Pure Non-Carbohydrate Compounds." ChemInform 28, no. 14 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199714287.

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48

FERRIER, R. J. "ChemInform Abstract: Synthesis of Enantiomerically Pure Non-Carbohydrate Compounds." ChemInform 27, no. 27 (August 5, 2010): no. http://dx.doi.org/10.1002/chin.199627286.

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49

Errécalde, Olivier, Michel Astruc, Georges Maury, and Raoul Pinel. "Biotransformation of butyltin compounds using pure strains of microorganisms." Applied Organometallic Chemistry 9, no. 1 (February 1995): 23–28. http://dx.doi.org/10.1002/aoc.590090105.

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Anon., Anon. "ChemInform Abstract: Synthesis of Enantiomerically Pure Non-Carbohydrate Compounds." ChemInform 30, no. 23 (June 15, 2010): no. http://dx.doi.org/10.1002/chin.199923322.

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