Статті в журналах з теми "Aromatic chemistry"
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Yan, Yingying, David Cabrera-Perez, Jintai Lin, Andrea Pozzer, Lu Hu, Dylan B. Millet, William C. Porter, and Jos Lelieveld. "Global tropospheric effects of aromatic chemistry with the SAPRC-11 mechanism implemented in GEOS-Chem version 9-02." Geoscientific Model Development 12, no. 1 (January 4, 2019): 111–30. http://dx.doi.org/10.5194/gmd-12-111-2019.
Повний текст джерелаLu, Zhengyu, Qin Zhu, Yuanting Cai, Zhixin Chen, Kaiyue Zhuo, Jun Zhu, Hong Zhang, and Haiping Xia. "Access to tetracyclic aromatics with bridgehead metals via metalla-click reactions." Science Advances 6, no. 3 (January 2020): eaay2535. http://dx.doi.org/10.1126/sciadv.aay2535.
Повний текст джерелаPlater, M. John. "4 Aromatic chemistry." Annual Reports Section "B" (Organic Chemistry) 96 (2000): 131–55. http://dx.doi.org/10.1039/b002149k.
Повний текст джерелаToyota, Shinji, Masahiko Iyoda, and Fumio Toda. "7 Aromatic chemistry." Annu. Rep. Prog. Chem., Sect. B: Org. Chem. 98 (2002): 359–407. http://dx.doi.org/10.1039/b111467k.
Повний текст джерелаYeston, J. "CHEMISTRY: Aromatic Surprise." Science 319, no. 5860 (January 11, 2008): 137d. http://dx.doi.org/10.1126/science.319.5860.137d.
Повний текст джерелаJones, R. C. F. "Aromatic heterocyclic chemistry." Trends in Pharmacological Sciences 13 (January 1992): 417–18. http://dx.doi.org/10.1016/0165-6147(92)90127-r.
Повний текст джерелаNewman, John W., and I. C. Lewis. "Industrial Aromatic Chemistry." Carbon 27, no. 3 (1989): 503–4. http://dx.doi.org/10.1016/0008-6223(89)90089-4.
Повний текст джерелаBosdet, Michael J. D., and Warren E. Piers. "B-N as a C-C substitute in aromatic systems." Canadian Journal of Chemistry 87, no. 1 (January 1, 2009): 8–29. http://dx.doi.org/10.1139/v08-110.
Повний текст джерелаParikh, Harshal M., Harvey E. Jeffries, Ken G. Sexton, Deborah J. Luecken, Richard M. Kamens, and William Vizuete. "Evaluation of aromatic oxidation reactions in seven chemical mechanisms with an outdoor chamber." Environmental Chemistry 10, no. 3 (2013): 245. http://dx.doi.org/10.1071/en13039.
Повний текст джерелаKrompiec, Stanisław, Aneta Kurpanik-Wójcik, Marek Matussek, Bogumiła Gołek, Angelika Mieszczanin, and Aleksandra Fijołek. "Diels–Alder Cycloaddition with CO, CO2, SO2, or N2 Extrusion: A Powerful Tool for Material Chemistry." Materials 15, no. 1 (December 27, 2021): 172. http://dx.doi.org/10.3390/ma15010172.
Повний текст джерелаWang, Miaomiao, and Yanlan Wang. "Advances for Triangular and Sandwich-Shaped All-Metal Aromatics." Molecules 29, no. 4 (February 7, 2024): 763. http://dx.doi.org/10.3390/molecules29040763.
Повний текст джерелаJohn Plater, M. "Chapter 4. Aromatic chemistry." Annual Reports Section "B" (Organic Chemistry) 94 (1998): 129. http://dx.doi.org/10.1039/oc094129.
Повний текст джерелаPlater, M. John. "Chapter 4. Aromatic chemistry." Annual Reports Section "B" (Organic Chemistry) 95 (1999): 137–56. http://dx.doi.org/10.1039/a808583h.
Повний текст джерелаSeo, D. K. "CHEMISTRY: Aromatic Metal Clusters." Science 291, no. 5505 (February 2, 2001): 841–42. http://dx.doi.org/10.1126/science.1058418.
Повний текст джерелаPlater, M. John. "ChemInform Abstract: Aromatic Chemistry." ChemInform 31, no. 18 (June 8, 2010): no. http://dx.doi.org/10.1002/chin.200018191.
Повний текст джерелаPlater, M. John. "ChemInform Abstract: Aromatic Chemistry." ChemInform 32, no. 22 (May 26, 2010): no. http://dx.doi.org/10.1002/chin.200122262.
Повний текст джерелаTogo, Hideo, and Sousuke Ushijima. "One-Pot Conversion of Aromatic Bromides and Aromatics into Aromatic Nitriles." Synlett 2010, no. 10 (May 10, 2010): 1562–66. http://dx.doi.org/10.1055/s-0029-1219935.
Повний текст джерелаColquhoun, Howard M., Mikhail G. Zolotukhin, Leonard M. Khalilov, and Usein M. Dzhemilev. "Superelectrophiles in Aromatic Polymer Chemistry." Macromolecules 34, no. 4 (February 2001): 1122–24. http://dx.doi.org/10.1021/ma001579o.
Повний текст джерелаCao, Xiao-Yu, Qianyi Zhao, Zhiqun Lin, and Haiping Xia. "The Chemistry of Aromatic Osmacycles." Accounts of Chemical Research 47, no. 2 (November 14, 2013): 341–54. http://dx.doi.org/10.1021/ar400087x.
Повний текст джерелаJin, Hanfeng, Wenhao Yuan, Wei Li, Jiuzhong Yang, Zhongyue Zhou, Long Zhao, Yuyang Li, and Fei Qi. "Combustion chemistry of aromatic hydrocarbons." Progress in Energy and Combustion Science 96 (May 2023): 101076. http://dx.doi.org/10.1016/j.pecs.2023.101076.
Повний текст джерелаDiederich, François, and Carlo Thilgen. "Preface." Pure and Applied Chemistry 82, no. 4 (January 1, 2010): iv. http://dx.doi.org/10.1351/pac20108204iv.
Повний текст джерелаJones, Lyn H., Nicholas W. Summerhill, Nigel A. Swain, and James E. Mills. "Aromatic chloride to nitrile transformation: medicinal and synthetic chemistry." MedChemComm 1, no. 5 (2010): 309–18. http://dx.doi.org/10.1039/c0md00135j.
Повний текст джерелаPostnikov, Pavel S., Marina Trusova, Ksenia Kutonova, and Viktor Filimonov. "Arenediazonium salts transformations in water media: Coming round to origins." Resource-Efficient Technologies, no. 1 (June 30, 2016): 36–42. http://dx.doi.org/10.18799/24056529/2016/1/37.
Повний текст джерелаŠmídl, Petr, and Karel Pecka. "Chromatographic behaviour of aromatic hydrocarbons and heterocyclic compounds on silica gel with a chemically bonded amino phase." Collection of Czechoslovak Chemical Communications 50, no. 11 (1985): 2375–80. http://dx.doi.org/10.1135/cccc19852375.
Повний текст джерелаLemaitre, Clément, Stefania Perulli, Ophélie Quinonero, Cyril Bressy, Jean Rodriguez, Thierry Constantieux, Olga García Mancheño, and Xavier Bugaut. "Enantioselective Synthesis of Atropisomers by Oxidative Aromatization with Central-to-Axial Conversion of Chirality." Molecules 28, no. 7 (March 31, 2023): 3142. http://dx.doi.org/10.3390/molecules28073142.
Повний текст джерелаSun, Laizhi, Zhibin Wang, Lei Chen, Shuangxia Yang, Xinping Xie, Mingjie Gao, Baofeng Zhao, Hongyu Si, Jian Li, and Dongliang Hua. "Catalytic Fast Pyrolysis of Biomass into Aromatic Hydrocarbons over Mo-Modified ZSM-5 Catalysts." Catalysts 10, no. 9 (September 12, 2020): 1051. http://dx.doi.org/10.3390/catal10091051.
Повний текст джерелаAbe, Daisuke, Yuichiro Fukuda, and Yuji Sasanuma. "Chemistry of aromatic polythioesters and polydithioesters." Polymer Chemistry 6, no. 16 (2015): 3131–42. http://dx.doi.org/10.1039/c4py01702a.
Повний текст джерелаPurchase, Rupert. "Polycyclic aromatic hydrocarbons: Chemistry and carcinogenicity." Food and Chemical Toxicology 30, no. 9 (September 1992): 819. http://dx.doi.org/10.1016/0278-6915(92)90088-3.
Повний текст джерелаLepp, S., and A. Dalgarno. "Polycyclic aromatic hydrocarbons in interstellar chemistry." Astrophysical Journal 324 (January 1988): 553. http://dx.doi.org/10.1086/165915.
Повний текст джерелаPlater, M. John. "ChemInform Abstract: Chapter 4: Aromatic Chemistry." ChemInform 30, no. 16 (June 16, 2010): no. http://dx.doi.org/10.1002/chin.199916285.
Повний текст джерелаPräsang, C., A. Mlodzianowska, G. Geiseler, W. Massa, M. Hofmann, and A. Berndt. "Two-electron aromatics containing three and four adjacent boron atoms." Pure and Applied Chemistry 75, no. 9 (January 1, 2003): 1175–82. http://dx.doi.org/10.1351/pac200375091175.
Повний текст джерелаBernstein, Max. "Reactions of aromatics in space and connections to the carbon chemistry of Solar System materials." Proceedings of the International Astronomical Union 4, S251 (February 2008): 437–40. http://dx.doi.org/10.1017/s1743921308022102.
Повний текст джерелаAbe, Daisuke, Yuichiro Fukuda, and Yuji Sasanuma. "Correction: Chemistry of aromatic polythioesters and polydithioesters." Polymer Chemistry 7, no. 8 (2016): 1682. http://dx.doi.org/10.1039/c6py90024k.
Повний текст джерелаMarquet, Jorge, Francisco Casado, Maria Cervera, Martirio Espin, Iluminada Gallardo, M. Mir, and M. Niat. "Reductively activated 'polar' nucleophilic aromatic substitution. A new mechanism in aromatic chemistry?" Pure and Applied Chemistry 67, no. 5 (January 1, 1995): 703–10. http://dx.doi.org/10.1351/pac199567050703.
Повний текст джерелаQiu, Rulin, and Jun Zhu. "Adaptive aromaticity in 16-valence-electron metallazapentalenes." Dalton Transactions 50, no. 45 (2021): 16842–48. http://dx.doi.org/10.1039/d1dt03244e.
Повний текст джерелаLahoutifard, N., M. Ammann, L. Gutzwiller, B. Ervens, and Ch George. "The impact of multiphase reactions of NO<sub>2</sub> with aromatics: a modelling approach." Atmospheric Chemistry and Physics Discussions 2, no. 1 (February 11, 2002): 147–72. http://dx.doi.org/10.5194/acpd-2-147-2002.
Повний текст джерелаJenkin, M. E., S. M. Saunders, V. Wagner, and M. J. Pilling. "Protocol for the development of the Master Chemical Mechanism, MCM v3 (Part B): tropospheric degradation of aromatic volatile organic compounds." Atmospheric Chemistry and Physics Discussions 2, no. 6 (November 7, 2002): 1905–38. http://dx.doi.org/10.5194/acpd-2-1905-2002.
Повний текст джерелаJenkin, M. E., S. M. Saunders, V. Wagner, and M. J. Pilling. "Protocol for the development of the Master Chemical Mechanism, MCM v3 (Part B): tropospheric degradation of aromatic volatile organic compounds." Atmospheric Chemistry and Physics 3, no. 1 (February 12, 2003): 181–93. http://dx.doi.org/10.5194/acp-3-181-2003.
Повний текст джерелаCui, Weihong, and Bradford B. Wayland. "Hydrocarbon C-H bond activation by rhodium porphyrins." Journal of Porphyrins and Phthalocyanines 08, no. 02 (February 2004): 103–10. http://dx.doi.org/10.1142/s108842460400009x.
Повний текст джерелаLewis, Michael, Shana Beg, Aimee Clements, Dianne Tran, and Kristine Waggoner. "The effect of substituent rotation on aromatic quadrupole moments." Canadian Journal of Chemistry 88, no. 1 (January 2010): 5–13. http://dx.doi.org/10.1139/v09-152.
Повний текст джерелаBates, Kelvin H., Daniel J. Jacob, Ke Li, Peter D. Ivatt, Mat J. Evans, Yingying Yan, and Jintai Lin. "Development and evaluation of a new compact mechanism for aromatic oxidation in atmospheric models." Atmospheric Chemistry and Physics 21, no. 24 (December 17, 2021): 18351–74. http://dx.doi.org/10.5194/acp-21-18351-2021.
Повний текст джерелаKaiser, Ralf I., and Nils Hansen. "An Aromatic Universe–A Physical Chemistry Perspective." Journal of Physical Chemistry A 125, no. 18 (April 7, 2021): 3826–40. http://dx.doi.org/10.1021/acs.jpca.1c00606.
Повний текст джерелаWakelam, Valentine, and Eric Herbst. "Polycyclic Aromatic Hydrocarbons in Dense Cloud Chemistry." Astrophysical Journal 680, no. 1 (June 10, 2008): 371–83. http://dx.doi.org/10.1086/587734.
Повний текст джерелаSnieckus, Victor, and Paul Knochel. "Cluster Preface: Resurgence of Synthetic Aromatic Chemistry." Synlett 26, no. 20 (December 7, 2015): 2782–83. http://dx.doi.org/10.1055/s-0035-1560959.
Повний текст джерелаMinisci, F. "Diazo Chemistry I. Aromatic and Heteroaromatic Compounds." Synthesis 1995, no. 04 (April 1995): 473–74. http://dx.doi.org/10.1055/s-1995-3912.
Повний текст джерелаNodin, Laura, Olivier Noël, Françoise Chaminade, Ouerdia Maskri, Vincent Barbier, Olivier David, Philippe Fossé, and Juan Xie. "RNA SHAPE chemistry with aromatic acylating reagents." Bioorganic & Medicinal Chemistry Letters 25, no. 3 (February 2015): 566–70. http://dx.doi.org/10.1016/j.bmcl.2014.12.020.
Повний текст джерелаBartle, K. D. "Industrial Aromatic Chemistry, Raw Materials—Processes—Products." Fuel 67, no. 9 (September 1988): 1310. http://dx.doi.org/10.1016/0016-2361(88)90057-9.
Повний текст джерелаFreeman, Harold. "Aromatic amines: use in azo dye chemistry." Frontiers in Bioscience 18, no. 1 (2013): 145. http://dx.doi.org/10.2741/4093.
Повний текст джерелаGriffiths, J. "Diazo chemistry I: Aromatic and heteroatomic compounds." Dyes and Pigments 27, no. 3 (January 1995): 261–62. http://dx.doi.org/10.1016/0143-7208(95)90005-5.
Повний текст джерелаZANDER, M. "ChemInform Abstract: Aspects of Polycyclic Aromatic Chemistry." ChemInform 26, no. 9 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199509315.
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