Статті в журналах з теми "Aromatico"
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Lanati, Donato, Dora Marchi, Giacomo Mazza, Desislava Baicheva, and Alberto La Rosa. "Profilo aromatico varietale delle uve Mavrud, Bouquet e Rubin." BIO Web of Conferences 9 (2017): 02035. http://dx.doi.org/10.1051/bioconf/20170902035.
Повний текст джерелаTang, Jianhong, Jiarong Li, Lijun Zhang, Shuling Ma, Daxin Shi, Qi Zhang, Liupan Yang, Xiuzhen Wang, Xuan Liu, and Change Liu. "The Divergent Transformations of Aromatico-Aminonitrile with Carbonyl Compound." Journal of Heterocyclic Chemistry 49, no. 3 (May 2012): 533–42. http://dx.doi.org/10.1002/jhet.804.
Повний текст джерелаNaidu, Devendra, and Stephen W. Ragsdale. "Characterization of a Three-Component Vanillate O-Demethylase from Moorella thermoacetica." Journal of Bacteriology 183, no. 11 (June 1, 2001): 3276–81. http://dx.doi.org/10.1128/jb.183.11.3276-3281.2001.
Повний текст джерелаMachovina, Melodie M., Sam J. B. Mallinson, Brandon C. Knott, Alexander W. Meyers, Marc Garcia-Borràs, Lintao Bu, Japheth E. Gado, et al. "Enabling microbial syringol conversion through structure-guided protein engineering." Proceedings of the National Academy of Sciences 116, no. 28 (June 24, 2019): 13970–76. http://dx.doi.org/10.1073/pnas.1820001116.
Повний текст джерелаYang, Junjuan, Daxin Shi, Mingxing Liu, Lijun Zhang, Qi Zhang, and Jiarong Li. "Structure of the Condensed Product of Aromatico-Aminonitrile with Carbonyl Compound and Its Mechanism." Chinese Journal of Organic Chemistry 34, no. 12 (2014): 2424. http://dx.doi.org/10.6023/cjoc201406007.
Повний текст джерелаKancherla, Sindhu, Marianne Lorentzen, Victor Snieckus, and Kåre B. Jørgensen. "Directedortho-Metalation and Anionicortho-Fries Rearrangement of Polycyclic AromaticO-Carbamates: Regioselective Synthesis of Substituted Chrysenes." Journal of Organic Chemistry 83, no. 7 (March 15, 2018): 3590–98. http://dx.doi.org/10.1021/acs.joc.7b03210.
Повний текст джерелаShuvaev, Sergey, Ivan S. Bushmarinov, Ilya Sinev, Artem O. Dmitrienko, Konstantin A. Lyssenko, Vladimir Baulin, Wolfgang Grünert, Aslan Yu Tsivadze, and Natalia Kuzmina. "Copper(II) Complexes with Aromatico-Phosphorylated Phenols - Synthesis, Crystal Structures, and X-ray Photoelectron Spectroscopy." European Journal of Inorganic Chemistry 2013, no. 27 (July 10, 2013): 4823–31. http://dx.doi.org/10.1002/ejic.201300540.
Повний текст джерелаKudlich, Michael, Malcolm J. Hetheridge, Hans-Joachim Knackmuss, and Andreas Stolz. "Autoxidation Reactions of Different Aromatico-Aminohydroxynaphthalenes That Are Formed during the Anaerobic Reduction of Sulfonated Azo Dyes." Environmental Science & Technology 33, no. 6 (March 1999): 896–901. http://dx.doi.org/10.1021/es9808346.
Повний текст джерелаZhao, Kai Yun, Dong Bei Yue, and Ting Yang. "Characterization of Aromatics at Working Surface of a Municipal Solid Waste Landfill." Applied Mechanics and Materials 768 (June 2015): 458–64. http://dx.doi.org/10.4028/www.scientific.net/amm.768.458.
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 джерелаKonopski, Leszek, and Anna Kiełczewska. "Application of 2-Trichloromethylbenzimidazole in Analytical Chemistry: A Highly Selective Chromogenic Reagent for Thin-Layer Chromatography and Some Other Analytical Uses." Journal of Analytical Methods in Chemistry 2012 (2012): 1–10. http://dx.doi.org/10.1155/2012/650150.
Повний текст джерелаOttersbach, Philipp A., Paul W. Elsinghorst, Hans-Georg Häcker, and Michael Gütschow. "Direct Formation of Ring-Fused 1,3-Thiazine-2,4-dithiones from Aromatico-Amino Carboxylic Acids: Observation of a Carbon Disulfide Mediated Thionation." Organic Letters 12, no. 16 (August 20, 2010): 3662–65. http://dx.doi.org/10.1021/ol101471g.
Повний текст джерелаCosta Pessoa, João, Susana Marcão, Isabel Correia, Gisela Gonçalves, Agnes Dörnyei, Tamás Kiss, Tamás Jakusch, et al. "Vanadium (IV and V) Complexes of Reduced Schiff Bases Derived from the Reaction of Aromatico-Hydroxyaldehydes and Diamines Containing Carboxyl Groups." European Journal of Inorganic Chemistry 2006, no. 18 (September 2006): 3595–606. http://dx.doi.org/10.1002/ejic.200600309.
Повний текст джерелаLinz, Alexandra M., Yanjun Ma, Samuel Scholz, Daniel R. Noguera, and Timothy J. Donohue. "iNovo479: Metabolic Modeling Provides a Roadmap to Optimize Bioproduct Yield from Deconstructed Lignin Aromatics by Novosphingobium aromaticivorans." Metabolites 12, no. 4 (April 18, 2022): 366. http://dx.doi.org/10.3390/metabo12040366.
Повний текст джерелаPutrawan, I. Dewa Gede Arsa. "Aqueous liquid membrane process for recovery of BTX aromatics." Jurnal Teknik Kimia Indonesia 11, no. 1 (October 2, 2018): 1. http://dx.doi.org/10.5614/jtki.2012.11.1.1.
Повний текст джерелаWu, Xiaoping, Lijuan Zhu, Changhui Zhu, Chenguang Wang, and Quanxin Li. "Catalytic Transformation of Bio-oil to Benzaldehyde and Benzoic Acid: An Approach for the Production of High-value Aromatic Bio-chemicals." Current Green Chemistry 6, no. 2 (October 25, 2019): 135–46. http://dx.doi.org/10.2174/2213346106666190830114619.
Повний текст джерелаAklujkar, Muktak, Carla Risso, Jessica Smith, Derek Beaulieu, Ryan Dubay, Ludovic Giloteaux, Kristin DiBurro, and Dawn Holmes. "Anaerobic degradation of aromatic amino acids by the hyperthermophilic archaeon Ferroglobus placidus." Microbiology 160, no. 12 (December 1, 2014): 2694–709. http://dx.doi.org/10.1099/mic.0.083261-0.
Повний текст джерелаBerti, G., JE Moore, L. Salusinszky, and D. Seddon. "The Conversion of Light Naphtha Into Aromatics by Using Promoted Zeolite Catalysts." Australian Journal of Chemistry 42, no. 12 (1989): 2095. http://dx.doi.org/10.1071/ch9892095.
Повний текст джерелаYan, 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 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 джерелаSetiadi, Raka Nugraha Wijaya, and Danestyan Arif Pradana. "Producing monoaromatic compounds from pyrolytic vapour of rice straw using H-ZSM-5/B2O3 catalyst." E3S Web of Conferences 67 (2018): 02026. http://dx.doi.org/10.1051/e3sconf/20186702026.
Повний текст джерелаBasu, Aditya, Rahul Shrivastava, Bhakti Basu, Shree K. Apte, and Prashant S. Phale. "Modulation of Glucose Transport Causes Preferential Utilization of Aromatic Compounds in Pseudomonas putida CSV86." Journal of Bacteriology 189, no. 21 (September 7, 2007): 7556–62. http://dx.doi.org/10.1128/jb.01235-07.
Повний текст джерелаWang, Ting, Yuebing Xu, Chengming Shi, Feng Jiang, Bing Liu, and Xiaohao Liu. "Direct production of aromatics from syngas over a hybrid FeMn Fischer–Tropsch catalyst and HZSM-5 zeolite: local environment effect and mechanism-directed tuning of the aromatic selectivity." Catalysis Science & Technology 9, no. 15 (2019): 3933–46. http://dx.doi.org/10.1039/c9cy00750d.
Повний текст джерелаFoght, J. M., P. M. Fedorak, and D. W. S. Westlake. "Mineralization of [14C]hexadecane and [14C]phenanthrene in crude oil: specificity among bacterial isolates." Canadian Journal of Microbiology 36, no. 3 (March 1, 1990): 169–75. http://dx.doi.org/10.1139/m90-030.
Повний текст джерелаZhang, Lingling, Hong Yi, Jue Wang, and Aiwen Lei. "Visible-light induced oxidative Csp3–H activation of methyl aromatics to methyl esters." Green Chemistry 18, no. 19 (2016): 5122–26. http://dx.doi.org/10.1039/c6gc01880g.
Повний текст джерелаPourjafar, Mohammad, Amir Khosravani, and Rabi Behrooz. "Formation mechanism of aromatics during co-pyrolysis of coal and cotton stalk." BioResources 15, no. 2 (April 27, 2020): 4449–63. http://dx.doi.org/10.15376/biores.15.2.4449-4463.
Повний текст джерелаCorreia, Isabel, Jo�o Costa Pessoa, M. Teresa Duarte, M. F�tima Minas da Piedade, Tam�s Jackush, Tam�s Kiss, M. Margarida C. A. Castro, Carlos F. G. C. Geraldes, and Fernando Avecilla. "Vanadium(IV andV) Complexes of Schiff Bases and Reduced Schiff Bases Derived from the Reaction of Aromatico-Hydroxyaldehydes and Diamines: Synthesis, Characterisation and Solution Studies." European Journal of Inorganic Chemistry 2005, no. 4 (February 2005): 732–44. http://dx.doi.org/10.1002/ejic.200400481.
Повний текст джерелаWang, Weiyan, Zhiqiang Qiao, Kun Zhang, Pengli Liu, Yunquan Yang, and Kui Wu. "Highly selective catalytic hydrodeoxygenation of Caromatic–OH in bio-oil to cycloalkanes on a Ce–Ni–W–B amorphous catalyst." RSC Adv. 4, no. 70 (2014): 37288–95. http://dx.doi.org/10.1039/c4ra04364b.
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 джерелаVeličković, Dušan, Mowei Zhou, Jonathan S. Schilling, and Jiwei Zhang. "Using MALDI-FTICR-MS Imaging to Track Low-Molecular-Weight Aromatic Derivatives of Fungal Decayed Wood." Journal of Fungi 7, no. 8 (July 28, 2021): 609. http://dx.doi.org/10.3390/jof7080609.
Повний текст джерелаMa, Yanjun, Timothy J. Donohue, and Daniel R. Noguera. "Kinetic modeling of anaerobic degradation of plant-derived aromatic mixtures by Rhodopseudomonas palustris." Biodegradation 32, no. 2 (March 6, 2021): 179–92. http://dx.doi.org/10.1007/s10532-021-09932-3.
Повний текст джерелаCai, Yuanting, Yuhui Hua, Zhengyu Lu, Qing Lan, Zuzhang Lin, Jiawei Fei, Zhixin Chen, Hong Zhang, and Haiping Xia. "Electrophilic aromatic substitution reactions of compounds with Craig-Möbius aromaticity." Proceedings of the National Academy of Sciences 118, no. 39 (September 20, 2021): e2102310118. http://dx.doi.org/10.1073/pnas.2102310118.
Повний текст джерелаBasu, Aditya, Shree K. Apte, and Prashant S. Phale. "Preferential Utilization of Aromatic Compounds over Glucose by Pseudomonas putida CSV86." Applied and Environmental Microbiology 72, no. 3 (March 2006): 2226–30. http://dx.doi.org/10.1128/aem.72.3.2226-2230.2006.
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 джерелаAbonia, Rodrigo, Juan Castillo, Paola Cuervo, Braulio Insuasty, Jairo Quiroga, Alejandro OrtÃz, Manuel Nogueras, and Justo Cobo. "A Simple One-Pot Synthesis of New Imidazol-2-yl-1H-quinolin-2-ones from the Direct Reaction of 2-Chloroquinolin-3-carbaldehyde with Aromatico-Diamines." European Journal of Organic Chemistry 2010, no. 2 (January 2010): 317–25. http://dx.doi.org/10.1002/ejoc.200901014.
Повний текст джерелаChen, Yaqi, Tao Li, Jianguo Li, Shiyan Cheng, Jinghui Wang, Chandra Verma, Yibing Zhao, and Chuanliu Wu. "Stabilization of peptides against proteolysis through disulfide-bridged conjugation with synthetic aromatics." Organic & Biomolecular Chemistry 15, no. 8 (2017): 1921–29. http://dx.doi.org/10.1039/c6ob02786e.
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 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 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 джерелаWei, Zhimin, Youming Li, and Yi Hou. "Quick estimation for pollution load contributions of aromatic organics in wastewater from pulp and paper industry." Nordic Pulp & Paper Research Journal 33, no. 3 (September 25, 2018): 568–72. http://dx.doi.org/10.1515/npprj-2018-3046.
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 джерелаFedik, Nikita, Alexander I. Boldyrev та Alvaro Muñoz-Castro. "Aromatic character of [Au13]5+ and [MAu12]4+/6+ (M = Pd, Pt) cores in ligand protected gold nanoclusters – interplay between spherical and planar σ-aromatics". Physical Chemistry Chemical Physics 21, № 45 (2019): 25215–19. http://dx.doi.org/10.1039/c9cp04477a.
Повний текст джерелаSadowsky, Daniel, Kristopher McNeill, and Christopher J. Cramer. "Dehalogenation of Aromatics by Nucleophilic Aromatic Substitution." Environmental Science & Technology 48, no. 18 (August 27, 2014): 10904–11. http://dx.doi.org/10.1021/es5028822.
Повний текст джерелаToda, Hayato, Nobuyuki Hara, Michiya Fujiki, and Yoshitane Imai. "Sign inversion in magnetic circularly polarised luminescence of fused aromatics with 1.6 T N-up/S-up Faraday geometry." RSC Advances 11, no. 3 (2021): 1581–85. http://dx.doi.org/10.1039/d0ra09233a.
Повний текст джерелаARZHANIK, VLADIMIR, DARJA SVISTUNOVA, OLEG KOLIASNIKOV та ALEXEY M. EGOROV. "INTERACTION OF ANTIBODIES WITH AROMATIC LIGANDS: THE ROLE OF π-STACKING". Journal of Bioinformatics and Computational Biology 08, № 03 (червень 2010): 471–83. http://dx.doi.org/10.1142/s0219720010004835.
Повний текст джерелаWang, Wenbo, Zhongyang Luo, Simin Li, Shuang Xue, and Haoran Sun. "Novel Micro-Mesoporous Composite ZSM-5 Catalyst for Aromatics Production by Catalytic Fast Pyrolysis of Lignin Residues." Catalysts 10, no. 4 (April 1, 2020): 378. http://dx.doi.org/10.3390/catal10040378.
Повний текст джерелаAxelsson, Håkan, Anders Eilard, Annika Emanuelsson, Bo Galle, Hans Edner, Pär Ragnarson, and Henrik Kloo. "Measurement of Aromatic Hydrocarbons with the DOAS Technique." Applied Spectroscopy 49, no. 9 (September 1995): 1254–60. http://dx.doi.org/10.1366/0003702953965254.
Повний текст джерелаMcKee, Richard H., Ceinwen A. Schreiner, Russell White, Mark Saperstein, Jeffrey H. Charlap, Thomas P. O'Neill, Katy Olsavsky Goyak, and Mark Nicolich. "Characterization of the Noncancer Hazards of Gas Oils." International Journal of Toxicology 33, no. 1_suppl (October 31, 2013): 78S—94S. http://dx.doi.org/10.1177/1091581813504228.
Повний текст джерелаZhou, Haifeng, Yasuhiro Uozumi, Danyi Chen, Yanmei Zhou, Sensheng Liu, Qixing Liu, and Kaili Zhang. "Metal-free Reduction of Nitro Aromatics to Amines with B2(OH)4/H2O." Synlett 29, no. 13 (June 19, 2018): 1765–68. http://dx.doi.org/10.1055/s-0037-1610086.
Повний текст джерелаPeng, Jianfei, Min Hu, Zhuofei Du, Yinhui Wang, Jing Zheng, Wenbin Zhang, Yudong Yang, et al. "Gasoline aromatics: a critical determinant of urban secondary organic aerosol formation." Atmospheric Chemistry and Physics 17, no. 17 (September 13, 2017): 10743–52. http://dx.doi.org/10.5194/acp-17-10743-2017.
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