Artigos de revistas sobre o tema "Alkyl-quinolones"
Crie uma referência precisa em APA, MLA, Chicago, Harvard, e outros estilos
Veja os 50 melhores artigos de revistas para estudos sobre o assunto "Alkyl-quinolones".
Ao lado de cada fonte na lista de referências, há um botão "Adicionar à bibliografia". Clique e geraremos automaticamente a citação bibliográfica do trabalho escolhido no estilo de citação de que você precisa: APA, MLA, Harvard, Chicago, Vancouver, etc.
Você também pode baixar o texto completo da publicação científica em formato .pdf e ler o resumo do trabalho online se estiver presente nos metadados.
Veja os artigos de revistas das mais diversas áreas científicas e compile uma bibliografia correta.
Liu, Huanhuan, Huadan Liu, Enhua Wang, Liangqun Li, Zhongsheng Luo, Jiafu Cao, Jialin Chen, Lishou Yang e Xiaosheng Yang. "Hydrogen Bond Assisted Three-Component Tandem Reactions to Access N-Alkyl-4-Quinolones". Molecules 28, n.º 5 (2 de março de 2023): 2304. http://dx.doi.org/10.3390/molecules28052304.
Texto completo da fonteMollova-Sapundzhieva, Yordanka, Plamen Angelov, Danail Georgiev e Pavel Yanev. "Synthetic approach to 2-alkyl-4-quinolones and 2-alkyl-4-quinolone-3-carboxamides based on common β-keto amide precursors". Beilstein Journal of Organic Chemistry 19 (23 de novembro de 2023): 1804–10. http://dx.doi.org/10.3762/bjoc.19.132.
Texto completo da fonteTang, Jing, e Xian Huang. "Convenient synthesis of 5-(Arylamino(Alkylthio)Methylene)-2,2-Dimethyl-1,3-Dioxane-4,6-Diones and 2-Arylthio-4-Quinolones". Journal of Chemical Research 2003, n.º 3 (março de 2003): 140–41. http://dx.doi.org/10.3184/030823403103173264.
Texto completo da fonteBezuglyi, P. A., I. V. Ukrainets, V. I. Treskach e A. V. Turov. "4-Hydroxy-2-quinolones. 1. Efficient method for obtaining 3-alkyl-4-hydroxy-2-quinolones". Chemistry of Heterocyclic Compounds 27, n.º 11 (novembro de 1991): 1237–38. http://dx.doi.org/10.1007/bf00471752.
Texto completo da fonteSaalim, Muhammad, Jessica Villegas-Moreno e Benjamin R. Clark. "Bacterial Alkyl-4-quinolones: Discovery, Structural Diversity and Biological Properties". Molecules 25, n.º 23 (2 de dezembro de 2020): 5689. http://dx.doi.org/10.3390/molecules25235689.
Texto completo da fonteVrla, Geoffrey D., Mark Esposito, Chen Zhang, Yibin Kang, Mohammad R. Seyedsayamdost e Zemer Gitai. "Cytotoxic alkyl-quinolones mediate surface-induced virulence in Pseudomonas aeruginosa". PLOS Pathogens 16, n.º 9 (14 de setembro de 2020): e1008867. http://dx.doi.org/10.1371/journal.ppat.1008867.
Texto completo da fonteBEZUGLYI, P. A., I. V. UKRAINETS, V. I. TRESKATCH e A. V. TUROV. "ChemInform Abstract: 4-Hydroxy-2-quinolones. Part 1. Effective Preparation of 3-Alkyl-4- hydroxy-2-quinolones." ChemInform 24, n.º 37 (20 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199337226.
Texto completo da fonteChen, Bang-chi, Xian Huang e Jin Wang. "A Versatile Synthesis of 2-Alkyl and 2-Aryl 4-Quinolones". Synthesis 1987, n.º 05 (1987): 482–83. http://dx.doi.org/10.1055/s-1987-33427.
Texto completo da fonteGupta, Rashmi, e Martin Schuster. "Quorum sensing modulates colony morphology through alkyl quinolones in Pseudomonas aeruginosa". BMC Microbiology 12, n.º 1 (2012): 30. http://dx.doi.org/10.1186/1471-2180-12-30.
Texto completo da fonteMichalet, S., P. M. Allard, C. Commun, V. T. Nguyen Ngoc, K. Nouwade, B. Gioia, M. G. Dijoux-Franca, J. L. Wolfender e A. Doléans-Jordheim. "ePS6.03 Alkyl-Quinolones derivatives could predict Pseudomonas infection chronicity in cystic fibrosis". Journal of Cystic Fibrosis 19 (junho de 2020): S52—S53. http://dx.doi.org/10.1016/s1569-1993(20)30331-3.
Texto completo da fonteAl-Qawasmeh, Raed, Jalal Zahra, Monther Khanfar, Yusuf AL-Hiari, Mustafa El-Abadelah e Wolfgang Voelter. "A Convenient Synthesis of 1-Alkyl-7-chloro-6-fluoro-3-nitro-4-quinolones". Letters in Organic Chemistry 6, n.º 6 (1 de setembro de 2009): 511–14. http://dx.doi.org/10.2174/157017809789124812.
Texto completo da fonteSong, Yoon Ju, Jin Sun Choi e Jae In Lee. "An Efficient Synthesis of 1-Alkyl-2-phenyl-4-quinolones from 2-Halobenzoic Acids". Bulletin of the Korean Chemical Society 34, n.º 10 (20 de outubro de 2013): 3117–20. http://dx.doi.org/10.5012/bkcs.2013.34.10.3117.
Texto completo da fonteDubern, Jean-Frédéric, e Stephen P. Diggle. "Quorum sensing by 2-alkyl-4-quinolones in Pseudomonas aeruginosa and other bacterial species". Molecular BioSystems 4, n.º 9 (2008): 882. http://dx.doi.org/10.1039/b803796p.
Texto completo da fonteNiewerth, Heiko, Klaus Bergander, Siri Ram Chhabra, Paul Williams e Susanne Fetzner. "Synthesis and biotransformation of 2-alkyl-4(1H)-quinolones by recombinant Pseudomonas putida KT2440". Applied Microbiology and Biotechnology 91, n.º 5 (14 de junho de 2011): 1399–408. http://dx.doi.org/10.1007/s00253-011-3378-0.
Texto completo da fonteLi, Dandan, Naoya Oku, Atsumi Hasada, Masafumi Shimizu e Yasuhiro Igarashi. "Two new 2-alkylquinolones, inhibitory to the fish skin ulcer pathogen Tenacibaculum maritimum, produced by a rhizobacterium of the genus Burkholderia sp." Beilstein Journal of Organic Chemistry 14 (14 de junho de 2018): 1446–51. http://dx.doi.org/10.3762/bjoc.14.122.
Texto completo da fonteRitzmann, Niklas H., Almuth Mährlein, Simon Ernst, Ulrich Hennecke, Steffen L. Drees e Susanne Fetzner. "Bromination of alkyl quinolones by Microbulbifer sp. HZ11, a marine Gammaproteobacterium, modulates their antibacterial activity". Environmental Microbiology 21, n.º 7 (6 de junho de 2019): 2595–609. http://dx.doi.org/10.1111/1462-2920.14654.
Texto completo da fonteUkrainets, I. V., S. G. Taran, O. A. Evtifeeva, O. V. Gorokhova, P. A. Bezuglyi, A. V. Turov, L. N. Voronina e N. I. Filimonova. "4-Hydroxy-2-quinolones 19. A new synthesis of 3-Alkyl-2-oxo-4-hydroxyquinolines". Chemistry of Heterocyclic Compounds 30, n.º 5 (maio de 1994): 591–95. http://dx.doi.org/10.1007/bf01169841.
Texto completo da fonteSáenz, Fabián E., Alexis N. LaCrue, R. Matthew Cross, Jordany R. Maignan, Kenneth O. Udenze, Roman Manetsch e Dennis E. Kyle. "4-(1H)-Quinolones and 1,2,3,4-Tetrahydroacridin-9(10H)-Ones Prevent the Transmission of Plasmodium falciparum to Anopheles freeborni". Antimicrobial Agents and Chemotherapy 57, n.º 12 (30 de setembro de 2013): 6187–95. http://dx.doi.org/10.1128/aac.00492-13.
Texto completo da fonteBarr, H., A. Fogarty, N. Halliday, A. Knox, B. Quon, D. Forrester, P. Williams, D. Barrett e M. Camara. "P92 Systemic alkyl quinolones as novel biomarkers for pulmonary exacerbations in cystic fibrosis: a validation study". Thorax 71, Suppl 3 (15 de novembro de 2016): A133.2—A134. http://dx.doi.org/10.1136/thoraxjnl-2016-209333.235.
Texto completo da fonteXu, Bin, Jun Shao, Xiaomei Huang, Xiaohu Hong e Bingxin Liu. "Synthesis of N-Alkyl-Substituted 4-Quinolones via Tandem Alkenyl and Aryl C-N Bond Formation". Synthesis 44, n.º 12 (3 de abril de 2012): 1798–805. http://dx.doi.org/10.1055/s-0031-1290775.
Texto completo da fonteLi, Jianye, Weiwei Sun, Muhammad Saalim, Guixiang Wei, Diana A. Zaleta-Pinet e Benjamin R. Clark. "Isolation of 2-Alkyl-4-quinolones with Unusual Side Chains from a Chinese Pseudomonas aeruginosa Isolate". Journal of Natural Products 83, n.º 7 (30 de junho de 2020): 2294–98. http://dx.doi.org/10.1021/acs.jnatprod.0c00026.
Texto completo da fonteLegendre, Claire, F. Jerry Reen, Marlies J. Mooij, Gerard P. McGlacken, Claire Adams e Fergal O'Gara. "Pseudomonas aeruginosa Alkyl Quinolones Repress Hypoxia-Inducible Factor 1 (HIF-1) Signaling through HIF-1α Degradation". Infection and Immunity 80, n.º 11 (4 de setembro de 2012): 3985–92. http://dx.doi.org/10.1128/iai.00554-12.
Texto completo da fontePistorius, Dominik, Angelika Ullrich, Simon Lucas, Rolf W. Hartmann, Uli Kazmaier e Rolf Müller. "Biosynthesis of 2-Alkyl-4(1H)-Quinolones in Pseudomonas aeruginosa: Potential for Therapeutic Interference with Pathogenicity". ChemBioChem 12, n.º 6 (18 de março de 2011): 850–53. http://dx.doi.org/10.1002/cbic.201100014.
Texto completo da fonteShui, Hongling, Yuhong Zhong, Renshi Luo, Zhanyi Zhang, Jiuzhong Huang, Ping Yang e Nianhua Luo. "Cyclometalated iridium complexes-catalyzed acceptorless dehydrogenative coupling reaction: construction of quinoline derivatives and evaluation of their antimicrobial activities". Beilstein Journal of Organic Chemistry 18 (27 de outubro de 2022): 1507–17. http://dx.doi.org/10.3762/bjoc.18.159.
Texto completo da fonteBarr, Helen L., Nigel Halliday, David A. Barrett, Paul Williams, Douglas L. Forrester, Daniel Peckham, Kate Williams et al. "Diagnostic and prognostic significance of systemic alkyl quinolones for P. aeruginosa in cystic fibrosis: A longitudinal study". Journal of Cystic Fibrosis 16, n.º 2 (março de 2017): 230–38. http://dx.doi.org/10.1016/j.jcf.2016.10.005.
Texto completo da fonteSong, Yoon Ju, Jin Sun Choi e Jae In Lee. "ChemInform Abstract: An Efficient Synthesis of 1-Alkyl-2-phenyl-4-quinolones (VII) from 2-Halobenzoic Acids." ChemInform 45, n.º 9 (14 de fevereiro de 2014): no. http://dx.doi.org/10.1002/chin.201409173.
Texto completo da fonteWube, Abraham, Juan-David Guzman, Antje Hüfner, Christina Hochfellner, Martina Blunder, Rudolf Bauer, Simon Gibbons, Sanjib Bhakta e Franz Bucar. "Synthesis and Antibacterial Evaluation of a New Series of N-Alkyl-2-alkynyl/(E)-alkenyl-4-(1H)-quinolones". Molecules 17, n.º 7 (9 de julho de 2012): 8217–40. http://dx.doi.org/10.3390/molecules17078217.
Texto completo da fonteShao, Jun, Xiaomei Huang, Xiaohu Hong, Bingxin Liu e Bin Xu. "ChemInform Abstract: Synthesis of N-Alkyl-Substituted 4-Quinolones via Tandem Alkenyl and Aryl C-N Bond Formation." ChemInform 43, n.º 41 (13 de setembro de 2012): no. http://dx.doi.org/10.1002/chin.201241156.
Texto completo da fonteRampioni, Giordano, Marilena Falcone, Stephan Heeb, Emanuela Frangipani, Matthew P. Fletcher, Jean-Frédéric Dubern, Paolo Visca, Livia Leoni, Miguel Cámara e Paul Williams. "Unravelling the Genome-Wide Contributions of Specific 2-Alkyl-4-Quinolones and PqsE to Quorum Sensing in Pseudomonas aeruginosa". PLOS Pathogens 12, n.º 11 (16 de novembro de 2016): e1006029. http://dx.doi.org/10.1371/journal.ppat.1006029.
Texto completo da fonteLin, San San, Stefan Kerscher, Ahmad Saleh, Ulrich Brandt, Uwe Groß e Wolfgang Bohne. "The Toxoplasma gondii type-II NADH dehydrogenase TgNDH2-I is inhibited by 1-hydroxy-2-alkyl-4(1H)quinolones". Biochimica et Biophysica Acta (BBA) - Bioenergetics 1777, n.º 11 (novembro de 2008): 1455–62. http://dx.doi.org/10.1016/j.bbabio.2008.08.006.
Texto completo da fonteBarr, H. L., N. Halliday, D. A. Barrett, P. Williams, D. L. Forrester, D. Peckham, K. Williams et al. "Diagnostic and prognostic significance of systemic alkyl quinolones for P. aeruginosa in cystic fibrosis: A longitudinal study; response to comments". Journal of Cystic Fibrosis 16, n.º 6 (novembro de 2017): e21. http://dx.doi.org/10.1016/j.jcf.2017.09.008.
Texto completo da fonteAyubi, Erfan, Jamal Hallajzadeh e Saeid Safiri. "Comment on data sparsity - Diagnostic and prognostic significance of systemic alkyl quinolones for P. aeruginosa in cystic fibrosis: A longitudinal study". Journal of Cystic Fibrosis 16, n.º 6 (novembro de 2017): e19-e20. http://dx.doi.org/10.1016/j.jcf.2017.07.012.
Texto completo da fonteUkrainets, L. V., O. V. Gorokhova, S. G. Taran, P. A. Bezulyi, A. V. Turov, N. A. Marusenko e O. A. Evtifeeva. "4-hydroxy-2-quinolones. 22.* Synthesis and biological properties of 1-alkyl(aryl)-2-oxo-3-carbethoxy-4-hydroxyquinolines and their derivatives". Chemistry of Heterocyclic Compounds 30, n.º 7 (julho de 1994): 829–36. http://dx.doi.org/10.1007/bf01169641.
Texto completo da fonteSeppänen, Otto, Mikko Muuronen e Juho Helaja. "Gold-Catalyzed Conversion of Aryl- and Alkyl-Substituted 1-(o-Aminophenyl)-2-propyn-1-ones to the Corresponding 2-Substituted 4-Quinolones". European Journal of Organic Chemistry 2014, n.º 19 (26 de maio de 2014): 4044–52. http://dx.doi.org/10.1002/ejoc.201402224.
Texto completo da fonteKilani-Feki, Olfa, Gérald Culioli, Annick Ortalo-Magné, Nabil Zouari, Yves Blache e Samir Jaoua. "Environmental Burkholderia cepacia Strain Cs5 Acting by Two Analogous Alkyl-Quinolones and a Didecyl-Phthalate Against a Broad Spectrum of Phytopathogens Fungi". Current Microbiology 62, n.º 5 (11 de fevereiro de 2011): 1490–95. http://dx.doi.org/10.1007/s00284-011-9892-6.
Texto completo da fonteSciscenko, Iván, Paula García-Negueroles, Ana María Amat, Isabel Oller, Carlos Escudero-Oñate, Laura Ferrando-Climent e Antonio Arques. "Use of Fluorescence Spectroscopy and Chemometrics to Visualise Fluoroquinolones Photodegradation Major Trends: A Confirmation Study with Mass Spectrometry". Molecules 28, n.º 2 (12 de janeiro de 2023): 777. http://dx.doi.org/10.3390/molecules28020777.
Texto completo da fonteUkrainets, I. V., N. L. Bereznyakova, V. A. Parshikov e O. V. Gorokhova. "4-Hydroxy-2-quinolones 150*. Efficient synthesis, structure, and biological activities of 4-methyl-2-oxo-1,2-dihydroquinoline-3-carboxylic acid alkyl amides". Chemistry of Heterocyclic Compounds 44, n.º 12 (dezembro de 2008): 1493–99. http://dx.doi.org/10.1007/s10593-009-0209-7.
Texto completo da fonteDow, Lachlan. "How Do Quorum-Sensing Signals Mediate Algae–Bacteria Interactions?" Microorganisms 9, n.º 7 (27 de junho de 2021): 1391. http://dx.doi.org/10.3390/microorganisms9071391.
Texto completo da fonteSeppaenen, Otto, Mikko Muuronen e Juho Helaja. "ChemInform Abstract: Gold-Catalyzed Conversion of Aryl- and Alkyl-Substituted 1-(o-Aminophenyl)-2-propyn-1-ones to the Corresponding 2-Substituted 4-Quinolones." ChemInform 46, n.º 8 (fevereiro de 2015): no. http://dx.doi.org/10.1002/chin.201508224.
Texto completo da fonteUkrainets, I. V., N. L. Bereznyakova, A. A. Davidenko e S. V. Slobodzian. "4-Hydroxy-2-quinolones. 167*. Study of the reaction of ethyl 1-alkyl-substituted 4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylates with phosphorus oxychloride". Chemistry of Heterocyclic Compounds 45, n.º 8 (agosto de 2009): 952–56. http://dx.doi.org/10.1007/s10593-009-0367-7.
Texto completo da fonteDepke, Tobias, Janne Gesine Thöming, Adrian Kordes, Susanne Häussler e Mark Brönstrup. "Untargeted LC-MS Metabolomics Differentiates Between Virulent and Avirulent Clinical Strains of Pseudomonas aeruginosa". Biomolecules 10, n.º 7 (13 de julho de 2020): 1041. http://dx.doi.org/10.3390/biom10071041.
Texto completo da fonteSingh, Shweta, Sharanya Nerella, Srihari Pabbaraja e Goverdhan Mehta. "Access to 2-Alkyl/Aryl-4-(1H)-Quinolones via Orthogonal “NH3” Insertion into o-Haloaryl Ynones: Total Synthesis of Bioactive Pseudanes, Graveoline, Graveolinine, and Waltherione F". Organic Letters 22, n.º 4 (4 de fevereiro de 2020): 1575–79. http://dx.doi.org/10.1021/acs.orglett.0c00172.
Texto completo da fonteUkrainets, I. V., I. A. Tugaibei, N. L. Bereznyakova, V. N. Kravchenko e A. V. Turov. "4-Hydroxy-2-quinolones 144. Alkyl-, arylalkyl-, and arylamides of 2-hydroxy-4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carboxylic acid and their diuretic properties". Chemistry of Heterocyclic Compounds 44, n.º 5 (maio de 2008): 565–75. http://dx.doi.org/10.1007/s10593-008-0076-7.
Texto completo da fonteUKRAINETS, I. V., O. V. GOROKHOVA, S. G. TARAN, P. A. BEZUGLYI, A. V. TUROV, N. A. MARUSENKO e O. A. EVTIFEEVA. "ChemInform Abstract: 4-Hydroxy-2-quinolones. Part 22. Synthesis and Biological Properties of 1-Alkyl(aryl)-2-oxo-3-carboethoxy-4-hydroxy-quinolines and Their Derivatives." ChemInform 26, n.º 18 (18 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199518153.
Texto completo da fonteNguyen, Angela T., Jace W. Jones, Max A. Ruge, Maureen A. Kane e Amanda G. Oglesby-Sherrouse. "Iron Depletion Enhances Production of Antimicrobials by Pseudomonas aeruginosa". Journal of Bacteriology 197, n.º 14 (27 de abril de 2015): 2265–75. http://dx.doi.org/10.1128/jb.00072-15.
Texto completo da fonteBrewer, Luke K., Jace W. Jones, Catherine B. Blackwood, Mariette Barbier, Amanda Oglesby-Sherrouse e Maureen A. Kane. "Development and bioanalytical method validation of an LC-MS/MS assay for simultaneous quantitation of 2-alkyl-4(1H)-quinolones for application in bacterial cell culture and lung tissue". Analytical and Bioanalytical Chemistry 412, n.º 7 (29 de janeiro de 2020): 1521–34. http://dx.doi.org/10.1007/s00216-019-02374-0.
Texto completo da fonteUkrainets, I. V., L. V. Sidorenko, A. A. Davidenko e A. K. Yarosh. "4-Hydroxy-2-quinolones. 174.* Hydrochlorides of [(alkylamino)alkyl]amides of 1-allyl- 4-hydroxy-6,7-dimethoxy-2-oxo-1,2-dihydro- quinoline-3-carboxylic acid – a new class of opioid receptor antagonists". Chemistry of Heterocyclic Compounds 46, n.º 4 (agosto de 2010): 445–51. http://dx.doi.org/10.1007/s10593-010-0529-7.
Texto completo da fonteUkrainets, I. V., L. V. Sidorenko, A. A. Davidenko e A. K. Yarosh. "ChemInform Abstract: 4-Hydroxy-2-quinolones. Part 174. Hydrochlorides of [(Alkylamino)alkyl]amides of 1-Allyl-4-hydroxy-6,7-dimethoxy-2-oxo-1,2-dihydroquinoline-3-carboxylic Acid - A New Class of Opiod Receptor Antagonists." ChemInform 42, n.º 4 (30 de dezembro de 2010): no. http://dx.doi.org/10.1002/chin.201104152.
Texto completo da fonteHuang, Bin, Yaqiu Long, Li-Rui Song, He Li, Shen-Feng Wang e Jian-Ping Lin. "Metal-free Hypervalent Iodine-promoted Tandem Carbonyl Migration and Unactivated C(Ph)-C(Alkyl) Bond Cleavage for Quinolone Scaffold Synthesis". Chemical Communications, 2022. http://dx.doi.org/10.1039/d2cc02245a.
Texto completo da fontePark, Cheol-Min, Jaehee Bae e Jiyoung Chae. "Synthesis of 2‐Quinolones based on Visible Light‐Catalyzed Annulation of Diazo compounds". Advanced Synthesis & Catalysis, 7 de fevereiro de 2024. http://dx.doi.org/10.1002/adsc.202301220.
Texto completo da fonte