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Journal articles on the topic 'Pimelic acid. Organic compounds'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Müller-Tautges, C., A. Eichler, M. Schwikowski, G. B. Pezzatti, M. Conedera, and T. Hoffmann. "Historic records of organic compounds from a high Alpine glacier: influences of biomass burning, anthropogenic emissions, and dust transport." Atmospheric Chemistry and Physics 16, no. 2 (2016): 1029–43. http://dx.doi.org/10.5194/acp-16-1029-2016.

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Abstract. Historic records of α-dicarbonyls (glyoxal, methylglyoxal), carboxylic acids (C6–C12 dicarboxylic acids, pinic acid, p-hydroxybenzoic acid, phthalic acid, 4-methylphthalic acid), and ions (oxalate, formate, calcium) were determined with annual resolution in an ice core from Grenzgletscher in the southern Swiss Alps, covering the time period from 1942 to 1993. Chemical analysis of the organic compounds was conducted using ultra-high-performance liquid chromatography (UHPLC) coupled to electrospray ionization high-resolution mass spectrometry (ESI-HRMS) for dicarbonyls and long-chain c

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2

Hansen, A. M. K., K. Kristensen, Q. T. Nguyen, et al. "Organosulfates and organic acids in Arctic aerosols: speciation, annual variation and concentration levels." Atmospheric Chemistry and Physics 14, no. 15 (2014): 7807–23. http://dx.doi.org/10.5194/acp-14-7807-2014.

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Abstract. Sources, composition and occurrence of secondary organic aerosols in the Arctic were investigated at Zeppelin Mountain, Svalbard, and Station Nord, northeastern Greenland, during the full annual cycle of 2008 and 2010, respectively. Speciation of organic acids, organosulfates and nitrooxy organosulfates – from both anthropogenic and biogenic precursors were in focus. A total of 11 organic acids (terpenylic acid, benzoic acid, phthalic acid, pinic acid, suberic acid, azelaic acid, adipic acid, pimelic acid, pinonic acid, diaterpenylic acid acetate and 3-methyl-1,2,3-butanetricarboxyli

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3

Amarandei, Cornelia, Romeo Iulian Olariu, and Cecilia Arsene. "Implications of Matrix Effects in Quantitative HPLC/ESI-ToF-MS Analyses of Atmospheric Organic Aerosols." Proceedings 55, no. 1 (2020): 6. http://dx.doi.org/10.3390/proceedings2020055006.

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Matrix-induced signal suppression or enhancements are known phenomena in electrospray ionization mass spectrometry. Very few studies report on method development for organic aerosols analyses with the evaluation of the matrix effects. The matrix effects lead to errors in the quantification of the analytes and affect the detection capability, precision, and accuracy of an analysis method. The present study reports on the matrix effects in the analysis of organic chemical compounds present in atmospheric aerosol particles collected on quartz filters. A total number of 19 analytes, including diff

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4

Martinsson, Johan, Guillaume Monteil, Moa K. Sporre, et al. "Exploring sources of biogenic secondary organic aerosol compounds using chemical analysis and the FLEXPART model." Atmospheric Chemistry and Physics 17, no. 18 (2017): 11025–40. http://dx.doi.org/10.5194/acp-17-11025-2017.

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Abstract. Molecular tracers in secondary organic aerosols (SOAs) can provide information on origin of SOA, as well as regional scale processes involved in their formation. In this study 9 carboxylic acids, 11 organosulfates (OSs) and 2 nitrooxy organosulfates (NOSs) were determined in daily aerosol particle filter samples from Vavihill measurement station in southern Sweden during June and July 2012. Several of the observed compounds are photo-oxidation products from biogenic volatile organic compounds (BVOCs). Highest average mass concentrations were observed for carboxylic acids derived from

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5

Marsh, Aleksandra, Rachael E. H. Miles, Grazia Rovelli, et al. "Influence of organic compound functionality on aerosol hygroscopicity: dicarboxylic acids, alkyl-substituents, sugars and amino acids." Atmospheric Chemistry and Physics 17, no. 9 (2017): 5583–99. http://dx.doi.org/10.5194/acp-17-5583-2017.

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Abstract. Hygroscopicity data for 36 organic compounds, including amino acids, organic acids, alcohols and sugars, are determined using a comparative kinetics electrodynamic balance (CK-EDB). The CK-EDB applies an electric field to trap-charged aqueous droplets in a chamber with controlled temperature and relative humidity (RH). The dual micro dispenser set-up allows for sequential trapping of probe and sample droplets for accurate determination of droplet water activities from 0.45 to > 0.99. Here, we validate and benchmark the CK-EDB for the homologous series of straight-chain dicarboxyli

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6

Kuwata, M., W. Shao, R. Lebouteiller, and S. T. Martin. "Classifying organic materials by oxygen-to-carbon elemental ratio to predict the activation regime of cloud condensation nuclei (CCN)." Atmospheric Chemistry and Physics Discussions 12, no. 12 (2012): 31829–70. http://dx.doi.org/10.5194/acpd-12-31829-2012.

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Abstract. The governing highly soluble, slightly soluble, or insoluble activation regime of organic compounds as cloud condensation nuclei (CCN) was examined as a function of oxygen-to-carbon elemental ratio (O : C). New data were collected for adipic, pimelic, suberic, azelaic and pinonic acids. Secondary organic materials (SOMs) produced by α-pinene ozonolysis and isoprene photo-oxidation were also included in the analysis. The saturation concentrations C of the organic compounds in aqueous solutions served as the key parameter for delineating regimes of CCN activation, and the values of C w

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7

Kuwata, M., W. Shao, R. Lebouteiller, and S. T. Martin. "Classifying organic materials by oxygen-to-carbon elemental ratio to predict the activation regime of Cloud Condensation Nuclei (CCN)." Atmospheric Chemistry and Physics 13, no. 10 (2013): 5309–24. http://dx.doi.org/10.5194/acp-13-5309-2013.

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Abstract. The governing highly soluble, slightly soluble, or insoluble activation regime of organic compounds as cloud condensation nuclei (CCN) was examined as a function of oxygen-to-carbon elemental ratio (O : C). New data were collected for adipic, pimelic, suberic, azelaic, and pinonic acids. Secondary organic materials (SOMs) produced by α-pinene ozonolysis and isoprene photo-oxidation were also included in the analysis. The saturation concentrations C of the organic compounds in aqueous solutions served as the key parameter for delineating regimes of CCN activation, and the values of C

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8

Broda, Jan, Marcin Baczek, Janusz Fabia, Dorota Binias та Ryszard Fryczkowski. "Nucleating agents based on graphene and graphene oxide for crystallization of the β-form of isotactic polypropylene". Journal of Materials Science 55, № 4 (2019): 1436–50. http://dx.doi.org/10.1007/s10853-019-04045-y.

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Abstract During the investigations, functionalization of graphene oxide synthesized using modified Hummers’ method and its reduced form was performed. Mixtures of graphene oxide and reduced graphene oxide with pimelic acid and calcium hydroxide were prepared for functionalization. During the reaction, the molecules of pimelic acid were attached to the surface of graphene sheets. By forming links between the carboxylic groups of pimelic acid and graphene oxide, the durable connection was achieved. The functionalized graphene oxide and the reduced graphene oxide were used as additives in isotact

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9

Ermer, Otto, Andreas Kusch, and Christof Röbke. "Distorted Fivefold-Diamond Structure of 4,4-Bis(2-carboxyethyl)pimelic Acid (‘Methanetetrapropionic Acid’)." Helvetica Chimica Acta 86, no. 4 (2003): 922–29. http://dx.doi.org/10.1002/hlca.200390110.

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10

Zhang, Wenting, Jian Sun, Fei Xu, et al. "Reactions of 2-Aminobenzohydrazide and 4-Oxo Pimelic Acid Catalyzed by Iodine in Ionic Liquids." Chinese Journal of Organic Chemistry 37, no. 12 (2017): 3191. http://dx.doi.org/10.6023/cjoc201706015.

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11

Wieczorkowska, Elzbieta, and Mervyn P. Hegarty. "Synthesis of DL-[7-14C]indospicine and DL-2-amino[7-14C]pimelic acid." Journal of Labelled Compounds and Radiopharmaceuticals 24, no. 11 (1987): 1273–80. http://dx.doi.org/10.1002/jlcr.2580241103.

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12

Huang, Liang, Li-Ping Zhang, and Lin-Pei Jin. "Hydrothermal synthesis and structural characterization of new lanthanide coordination polymers with pimelic acid and 1,10-phenanthroline." Journal of Molecular Structure 692, no. 1-3 (2004): 169–75. http://dx.doi.org/10.1016/j.molstruc.2004.01.027.

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13

Trongtorsak, Kessaraporn, Pitt Supaphol, and Supawan Tantayanon. "Effect of calcium stearate and pimelic acid addition on mechanical properties of heterophasic isotactic polypropylene/ethylene–propylene rubber blend." Polymer Testing 23, no. 5 (2004): 533–39. http://dx.doi.org/10.1016/j.polymertesting.2003.11.006.

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14

BERGMANN, E., та Lin CHUN-HSU. "Organic Fluorine Compounds; Part XLVI1. γ-Fluoroglutamic Acid and Fluorofolic Acid". Synthesis 1973, № 01 (2002): 44–46. http://dx.doi.org/10.1055/s-1973-22129.

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15

Hernáez, M. J., B. Floriano, J. J. Ríos, and E. Santero. "Identification of a Hydratase and a Class II Aldolase Involved in Biodegradation of the Organic Solvent Tetralin." Applied and Environmental Microbiology 68, no. 10 (2002): 4841–46. http://dx.doi.org/10.1128/aem.68.10.4841-4846.2002.

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ABSTRACT Two new genes whose products are involved in biodegradation of the organic solvent tetralin were identified. These genes, designated thnE and thnF, are located downstream of the previously identified thnD gene and code for a hydratase and an aldolase, respectively. A sequence comparison of enzymes similar to ThnE showed the significant similarity of hydratases involved in biodegradation pathways to 4-oxalocrotonate decarboxylases and established four separate groups of related enzymes. Consistent with the sequence information, characterization of the reaction catalyzed by ThnE showed

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16

Imai, Toru, Tomohiro Michitaka, and Akihito Hashidzume. "Formose reaction controlled by boronic acid compounds." Beilstein Journal of Organic Chemistry 12 (December 8, 2016): 2668–72. http://dx.doi.org/10.3762/bjoc.12.263.

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Formose reactions were carried out in the presence of low molecular weight and macromolecular boronic acid compounds, i.e., sodium phenylboronate (SPB) and a copolymer of sodium 4-vinylphenylboronate with sodium 4-styrenesulfonate (pVPB/NaSS), respectively. The boronic acid compounds provided different selectivities; sugars of a small carbon number were formed favorably in the presence of SPB, whereas sugar alcohols of a larger carbon number were formed preferably in the presence of pVPB/NaSS.

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17

Nishiyama, Tomihiro, Joanne F. Woodhall, Elvie N. Lawson, and William Kitching. "Synthesis of exogonic acid and related compounds." Journal of Organic Chemistry 54, no. 9 (1989): 2183–89. http://dx.doi.org/10.1021/jo00270a031.

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18

Xiang, Tao, and Keith P. Johnston. "Acid-Base Behavior of Organic Compounds in Supercritical Water." Journal of Physical Chemistry 98, no. 32 (1994): 7915–22. http://dx.doi.org/10.1021/j100083a027.

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19

Liu, Xing-Ping, Rama Krishna Narla, and Fatih M. Uckun. "Organic phenyl arsonic acid compounds with potent antileukemic activity." Bioorganic & Medicinal Chemistry Letters 13, no. 3 (2003): 581–83. http://dx.doi.org/10.1016/s0960-894x(02)00928-9.

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20

Ouryupin, Andrei B., Ivan A. Rakhov, and Tatyana A. Mastryukova. "Reactions of phosphorus acid halides withN-silylated organic compounds." Russian Chemical Reviews 67, no. 9 (1998): 749–59. http://dx.doi.org/10.1070/rc1998v067n09abeh000432.

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21

Mendonca, Gabriela, and Marcio Mattos. "Green Chlorination of Organic Compounds Using Trichloroisocyanuric Acid (TCCA)." Current Organic Synthesis 10, no. 6 (2014): 820–36. http://dx.doi.org/10.2174/157017941006140206102255.

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22

CANTRELL, G. L., and J. F. LANG. "ChemInform Abstract: Acid-Catalyzed Syntheses (of Organic Fluorine Compounds)." ChemInform 27, no. 51 (2010): no. http://dx.doi.org/10.1002/chin.199651250.

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23

Ishihara, Kazuaki, and Hisashi Yamamoto. "Arylboron Compounds as Acid Catalysts in Organic Synthetic Transformations." European Journal of Organic Chemistry 1999, no. 3 (1999): 527–38. http://dx.doi.org/10.1002/(sici)1099-0690(199903)1999:3<527::aid-ejoc527>3.0.co;2-r.

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24

Vishnetskaya, M. V., and M. Ya Mel’nikov. "Transformation of organic and inorganic compounds in trifluoroacetic acid." Russian Journal of Physical Chemistry A 90, no. 9 (2016): 1909–11. http://dx.doi.org/10.1134/s0036024416090314.

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25

de Lijser, H. J. P., P. Mulder, and R. Louw. "Thermal and acid catalyzed conversion of organic phosphorus compounds." Chemosphere 27, no. 5 (1993): 773–78. http://dx.doi.org/10.1016/0045-6535(93)90009-t.

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26

Brewer, J. R., J. R. Jones, K. W. M. Lawrie, D. Saunders, and A. Simmonds. "Tritiation of organic compounds by polymer-supported acid catalysts." Journal of Labelled Compounds and Radiopharmaceuticals 34, no. 4 (1994): 391–400. http://dx.doi.org/10.1002/jlcr.2580340411.

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27

Alkorta, Ibon, Nadine Jagerovic, and José Elguero. "Theoretical study of cyameluric acid and related compounds." Arkivoc 2004, no. 4 (2004): 130–36. http://dx.doi.org/10.3998/ark.5550190.0005.415.

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28

Kodama, Tetsuya. "Eventful Synthetic Studies on Nucleic Acid Related Compounds." Journal of Synthetic Organic Chemistry, Japan 76, no. 5 (2018): 450–53. http://dx.doi.org/10.5059/yukigoseikyokaishi.76.450.

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29

Musatov, D. M., L. A. Sviridova, I. A. Motorina, I. F. Leshcheva, and G. A. Golubeva. "Interaction of 5-hydroxypyrazolidines with Ch-acid compounds." Chemistry of Heterocyclic Compounds 30, no. 4 (1994): 422–28. http://dx.doi.org/10.1007/bf01169935.

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30

Mumtaz, Amara, Kiran Saeed, Abid Mahmood, et al. "Bisthioureas of pimelic acid and 4-methylsalicylic acid derivatives as selective inhibitors of tissue-nonspecific alkaline phosphatase (TNAP) and intestinal alkaline phosphatase (IAP): Synthesis and molecular docking studies." Bioorganic Chemistry 101 (August 2020): 103996. http://dx.doi.org/10.1016/j.bioorg.2020.103996.

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31

Campbell, M. M., M. Sainsbury, and P. A. Searle. "The Biosynthesis and Synthesis of Shikimic Acid, Chorismic Acid, and Related Compounds." Synthesis 1993, no. 02 (1993): 179–93. http://dx.doi.org/10.1055/s-1993-25824.

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32

Zhang, Ying Long, Hai Bo Zhang, You Shuang Zhu, Ming Le Cao, Ming Qiang Ai, and Feng Huang. "Influences of Organic Compounds on Laccase Activity Tests." Applied Mechanics and Materials 416-417 (September 2013): 1702–7. http://dx.doi.org/10.4028/www.scientific.net/amm.416-417.1702.

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Organic compounds oxalic acid and ethylenediaminetetraacetic acid disodium salt-2-hydrate (EDTA Na2) were described as laccase inhibitors by forming complex compounds with the metal ions of the laccase. Their influence on laccase from Trametes hirsuta lg-9 and Rhus vernificera in different test systems utilizing 2, 2-azino-bis (3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) and 2, 6-dimethoxyphenol (DMP) as enzyme substrates were tested. Our study indicated that oxalic acid can influence the laccase activity determination mainly by changing the pH of the reaction system. The influences of both

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33

Gündüz, Turgut, Esma Kiliç, Mustafa Tastekin, and Güleren Ozkan. "Conductimetric titrations of symmetrical aliphatic dicarboxylic acids in solvents pyridine and pyridine–benzene mixtures." Canadian Journal of Chemistry 68, no. 3 (1990): 431–34. http://dx.doi.org/10.1139/v90-065.

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Nine symmetrical aliphatic dicarboxylic acids, namely oxalic, malonic, succinic, glutaric, adipic, pimelic, suberic, azelaic, and sebacic acids, were titrated conductimetrically with tetrabutylammonium hydroxide in pyridine and pyridine–benzene mixtures ((2 + 1), (1 + 1), (1 + 2), (1 + 3), and (1 + 4)). Titration curves of the acids exhibited two distinct and stoichiometric end-points in media of dielectric constants 13.5, 10.0, 8.2, 6.3, 5.3, and 4.7, respectively. The closer investigations of the titration curves revealed that three factors mainly influence the shapes of the titration curves

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34

Henao, Laura Domínguez, Riccardo Delli Compagni, Andrea Turolla, and Manuela Antonelli. "Disinfection by Peracetic Acid: Influence of Inorganic and Organic Compounds." Proceedings of the Water Environment Federation 2017, no. 9 (2017): 3083–89. http://dx.doi.org/10.2175/193864717822157766.

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35

Chang, Meei-ling, Shian-chee Wu, and Chih-yu Chen. "Diffusion of Volatile Organic Compounds in Pressed Humic Acid Disks." Environmental Science & Technology 31, no. 8 (1997): 2307–12. http://dx.doi.org/10.1021/es960903l.

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36

Muchuweti, Maud, Gretchen Zenda, Ashwell R. Ndhlala, and Abisha Kasiyamhuru. "Sugars, organic acid and phenolic compounds of Ziziphus mauritiana Fruit." European Food Research and Technology 221, no. 3-4 (2005): 570–74. http://dx.doi.org/10.1007/s00217-005-1204-6.

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37

Shaabani, Ahmad, Maryam Behnam, and Ali Hossein Rezayan. "Tungstophosphoric acid (H3PW12O40) catalyzed oxidation of organic compounds with NaBrO3." Catalysis Communications 10, no. 7 (2009): 1074–78. http://dx.doi.org/10.1016/j.catcom.2008.12.059.

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38

Del Rio, J. C., F. J. Gonzalez-Villa, and F. Martin. "Retention of organic compounds in a humic acid from lignite." Science of The Total Environment 81-82 (June 1989): 373–80. http://dx.doi.org/10.1016/0048-9697(89)90145-9.

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39

Legand, S., C. Bouyer, V. Dauvois, F. Casanova, D. Lebeau, and C. Lamouroux. "Uranium carbide dissolution in nitric acid: speciation of organic compounds." Journal of Radioanalytical and Nuclear Chemistry 302, no. 1 (2014): 27–39. http://dx.doi.org/10.1007/s10967-014-3409-2.

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40

Jafvert, Chad T. "Sorption of organic acid compounds to sediments: Initial model development." Environmental Toxicology and Chemistry 9, no. 10 (1990): 1259–68. http://dx.doi.org/10.1002/etc.5620091004.

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41

KURIHARA, Hideki, Kazuaki ISHIHARA, and Hisashi YAMAMOTO. "Recent Developments of Arylboron Compounds as Lewis Acid Catalysts." Journal of Synthetic Organic Chemistry, Japan 56, no. 1 (1998): 45–53. http://dx.doi.org/10.5059/yukigoseikyokaishi.56.45.

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42

Wei, Zhenzhong, Jiangfei Li, Zeyun Wang, Pinhua Li, and Yongqiu Wang. "Synthesis of 1,4-Dihydropyridine Compounds Catalyzed by Humic Acid." Chinese Journal of Organic Chemistry 37, no. 7 (2017): 1835. http://dx.doi.org/10.6023/cjoc201612055.

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43

Xu, Yuliang, and Hao Fang. "Research Progress towards Synthesis of Aryl Boronic Acid Compounds." Chinese Journal of Organic Chemistry 38, no. 4 (2018): 738. http://dx.doi.org/10.6023/cjoc201709045.

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44

Antonioletti, R., F. Bonadies, and Arrigo Scettri. "Lewis acid induced .alpha.-alkoxyalkylation of 1,3-dicarbonyl compounds." Journal of Organic Chemistry 53, no. 23 (1988): 5540–42. http://dx.doi.org/10.1021/jo00258a028.

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45

Yamamoto, Hisashi, Yanhua Zhang, and Kazutaka Shibatomi. "Lewis Acid Catalyzed Highly Selective Halogenation of Aromatic Compounds." Synlett, no. 18 (2005): 2837–42. http://dx.doi.org/10.1055/s-2005-918919.

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46

Deady, Leslie W., Maureen F. Mackay, and Dianne M. Werden. "Reactions of some quinazoline compounds with ethoxymethylenemalonic acid derivatives." Journal of Heterocyclic Chemistry 26, no. 1 (1989): 161–68. http://dx.doi.org/10.1002/jhet.5570260129.

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47

Bassin, Jatinder P., Richard J. Cremlyn, John M. Lynch, and Frederic J. Swinbourne. "CYCLISATION OF DIARYL COMPOUNDS WITH CHLOROSULFONIC ACID." Phosphorus, Sulfur, and Silicon and the Related Elements 78, no. 1-4 (1993): 55–70. http://dx.doi.org/10.1080/10426509308032422.

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48

Moreno-Ma紡s, Marcial, and Roser Pleixats. "Bicyclic Compounds Structurally Relted to Dehydroacetic Acid and Triacetic Acid Lactone." HETEROCYCLES 37, no. 1 (1994): 585. http://dx.doi.org/10.3987/rev-93-sr2.

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49

Kulkarni, B., S. Chattopadhyay, A. Chattopadhyay, and V. Mamdapur. "Synthesis of the Demospongic Compounds, (6Z, 11Z)-Octadecadienoic Acid and (6Z, 11Z)-Eicosadienoic Acid." Molecules 2, no. 12 (1997): 99. http://dx.doi.org/10.3390/20600099.

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50

Kulkarni, B., S. Chattopadhyay, A. Chattopadhyay, and V. Mamdapur. "Synthesis of the Demospongic Compounds, (6Z, 11Z)-Octadecadienoic Acid and (6Z, 11Z)-Eicosadienoic Acid." Molecules 2, no. 12 (1997): 3–6. http://dx.doi.org/10.3390/jan97p2.

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