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Journal articles on the topic 'Pure compounds'

Author: Grafiati

Published: 8 June 2024

Last updated: 31 July 2025

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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 (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 (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 (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 (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 (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 (2010): no. http://dx.doi.org/10.1002/chin.199211295.

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8

Bauer, Sebastian, Steffen Tschirschwitz, Peter Lönnecke, et al. "Enantiomerically Pure Bis(phosphanyl)carbaborane(12) Compounds." European Journal of Inorganic Chemistry 2009, no. 19 (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.

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10

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 (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 de

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11

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 (2021): 086002. http://dx.doi.org/10.1149/2162-8777/ac19c6.

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12

Rodriguez, Lyanne, Óscar A. Muñoz-Bernal, Eduardo Fuentes, Emilio Alvarez-Parrilla, and Iván Palomo. "Antiplatelet Activity of Phenolic Compounds-Fortified Merlot Wine and Pure Phenolic Compounds." Applied Sciences 14, no. 13 (2024): 5707. http://dx.doi.org/10.3390/app14135707.

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Red wines and their pomace are valuable sources of phenolic compounds (PCs), which have been proposed as potential contributors to their cardioprotective effect through the inhibition of platelet aggregation. The antiplatelet activity of an extract depends on its chemical composition, specifically the presence of certain phenolic compounds, as well as the interactions between them affecting biological activity. In order to assess the effect on platelet aggregation, we investigated the effect of the grape pomace PC enrichment of a Merlot wine, as well as the effect of the five major phenolic co

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13

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 (2013): 473–78. http://dx.doi.org/10.1127/0935-1221/2013/0025-2293.

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14

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 (2004): 385–409. http://dx.doi.org/10.1127/0028-3649/2004/2004-0385.

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15

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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16

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 (2012): 1359–66. http://dx.doi.org/10.1080/00397911.2010.539894.

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17

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

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18

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

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19

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 (2008): 46–58. http://dx.doi.org/10.1007/s11669-008-9425-6.

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20

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

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21

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

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22

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

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23

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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24

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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25

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 (2011): 1228–31. http://dx.doi.org/10.1016/j.foodchem.2011.05.108.

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26

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

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27

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

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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.

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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 (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 red

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29

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.

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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 (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 qu

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31

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 (2003): 557–66. http://dx.doi.org/10.1016/s0969-8043(03)00053-8.

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32

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 (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 activi

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33

Zhao, Luyang, Chao Chen, Zimeng Li, Dongdong Qi, and Jianzhuang Jiang. "Density functional theory study of pure octupolar porphyrazines with second-order nonlinear optical activity." Journal of Porphyrins and Phthalocyanines 18, no. 08n09 (2014): 715–20. http://dx.doi.org/10.1142/s1088424614500539.

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Delicately designed pure octupolar molecular compounds, tetra(triptycene)porphyrazine and its skeleton expanded derivatives have been studied on the basis of density functional theory. The pure octupolar contribution with better isotropy to the second-order nonlinear optical response for these compounds is revealed, with further investigation to the molecular size effects, as well as peripheral polarized substituent influences to the nonlinear optical response.

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34

Jiménez-Arellanes, Adelina, Rosalba León-Díaz, Mariana Meckes, et al. "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 iso

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35

Juckmeta, Thana, Pakakrong Thongdeeying та Arunporn Itharat. "Inhibitory Effect onβ-Hexosaminidase Release from RBL-2H3 Cells of Extracts and Some Pure Constituents of Benchalokawichian, a Thai Herbal Remedy, Used for Allergic Disorders". Evidence-Based Complementary and Alternative Medicine 2014 (2014): 1–8. http://dx.doi.org/10.1155/2014/828760.

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Introduction.Benchalokawichian (BCW), a Thai traditional herbal formulation, has long been used as antipyretic and to treat skin disorders. It comprises roots from five herbs:Ficus racemosa,Capparis micracantha,Clerodendrum petasites,Harrisonia perforata, andTiliacora triandra. This polyherbal remedy has recently been included in the Thailand National List of Essential Medicines (Herbal Products list).Methodology.A Bioassay-guided fractionation technique was used to evaluate antiallergy activities of crude extracts, and those obtained by the multistep column chromatography isolation of pure co

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36

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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37

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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38

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 (2001): 551–65. http://dx.doi.org/10.1111/j.1745-459x.2001.tb00320.x.

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39

Bert, F., P. Mendels, D. Bono, et al. "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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40

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

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41

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

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42

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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43

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 (1992): 1165–70. http://dx.doi.org/10.1351/pac199264081165.

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44

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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45

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

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46

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 (2016): 481–88. http://dx.doi.org/10.1063/1674-0068/29/cjcp1601010.

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47

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

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48

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

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49

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 (2010): 343–51. http://dx.doi.org/10.1002/fam.1057.

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50

FERRIER, R. J., R. BLATTNER, K. CLINCH, et al. "ChemInform Abstract: Synthesis of Enantiomerically Pure Non-Carbohydrate Compounds." ChemInform 28, no. 14 (2010): no. http://dx.doi.org/10.1002/chin.199714287.

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