Artykuły w czasopismach na temat „Alkyl-quinolones”
Utwórz poprawne odniesienie w stylach APA, MLA, Chicago, Harvard i wielu innych
Sprawdź 50 najlepszych artykułów w czasopismach naukowych na temat „Alkyl-quinolones”.
Przycisk „Dodaj do bibliografii” jest dostępny obok każdej pracy w bibliografii. Użyj go – a my automatycznie utworzymy odniesienie bibliograficzne do wybranej pracy w stylu cytowania, którego potrzebujesz: APA, MLA, Harvard, Chicago, Vancouver itp.
Możesz również pobrać pełny tekst publikacji naukowej w formacie „.pdf” i przeczytać adnotację do pracy online, jeśli odpowiednie parametry są dostępne w metadanych.
Przeglądaj artykuły w czasopismach z różnych dziedzin i twórz odpowiednie bibliografie.
Liu, Huanhuan, Huadan Liu, Enhua Wang, Liangqun Li, Zhongsheng Luo, Jiafu Cao, Jialin Chen, Lishou Yang i Xiaosheng Yang. "Hydrogen Bond Assisted Three-Component Tandem Reactions to Access N-Alkyl-4-Quinolones". Molecules 28, nr 5 (2.03.2023): 2304. http://dx.doi.org/10.3390/molecules28052304.
Pełny tekst źródłaMollova-Sapundzhieva, Yordanka, Plamen Angelov, Danail Georgiev i 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 (23.11.2023): 1804–10. http://dx.doi.org/10.3762/bjoc.19.132.
Pełny tekst źródłaTang, Jing, i 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, nr 3 (marzec 2003): 140–41. http://dx.doi.org/10.3184/030823403103173264.
Pełny tekst źródłaBezuglyi, P. A., I. V. Ukrainets, V. I. Treskach i A. V. Turov. "4-Hydroxy-2-quinolones. 1. Efficient method for obtaining 3-alkyl-4-hydroxy-2-quinolones". Chemistry of Heterocyclic Compounds 27, nr 11 (listopad 1991): 1237–38. http://dx.doi.org/10.1007/bf00471752.
Pełny tekst źródłaSaalim, Muhammad, Jessica Villegas-Moreno i Benjamin R. Clark. "Bacterial Alkyl-4-quinolones: Discovery, Structural Diversity and Biological Properties". Molecules 25, nr 23 (2.12.2020): 5689. http://dx.doi.org/10.3390/molecules25235689.
Pełny tekst źródłaVrla, Geoffrey D., Mark Esposito, Chen Zhang, Yibin Kang, Mohammad R. Seyedsayamdost i Zemer Gitai. "Cytotoxic alkyl-quinolones mediate surface-induced virulence in Pseudomonas aeruginosa". PLOS Pathogens 16, nr 9 (14.09.2020): e1008867. http://dx.doi.org/10.1371/journal.ppat.1008867.
Pełny tekst źródłaBEZUGLYI, P. A., I. V. UKRAINETS, V. I. TRESKATCH i A. V. TUROV. "ChemInform Abstract: 4-Hydroxy-2-quinolones. Part 1. Effective Preparation of 3-Alkyl-4- hydroxy-2-quinolones." ChemInform 24, nr 37 (20.08.2010): no. http://dx.doi.org/10.1002/chin.199337226.
Pełny tekst źródłaChen, Bang-chi, Xian Huang i Jin Wang. "A Versatile Synthesis of 2-Alkyl and 2-Aryl 4-Quinolones". Synthesis 1987, nr 05 (1987): 482–83. http://dx.doi.org/10.1055/s-1987-33427.
Pełny tekst źródłaGupta, Rashmi, i Martin Schuster. "Quorum sensing modulates colony morphology through alkyl quinolones in Pseudomonas aeruginosa". BMC Microbiology 12, nr 1 (2012): 30. http://dx.doi.org/10.1186/1471-2180-12-30.
Pełny tekst źródłaMichalet, S., P. M. Allard, C. Commun, V. T. Nguyen Ngoc, K. Nouwade, B. Gioia, M. G. Dijoux-Franca, J. L. Wolfender i A. Doléans-Jordheim. "ePS6.03 Alkyl-Quinolones derivatives could predict Pseudomonas infection chronicity in cystic fibrosis". Journal of Cystic Fibrosis 19 (czerwiec 2020): S52—S53. http://dx.doi.org/10.1016/s1569-1993(20)30331-3.
Pełny tekst źródłaAl-Qawasmeh, Raed, Jalal Zahra, Monther Khanfar, Yusuf AL-Hiari, Mustafa El-Abadelah i Wolfgang Voelter. "A Convenient Synthesis of 1-Alkyl-7-chloro-6-fluoro-3-nitro-4-quinolones". Letters in Organic Chemistry 6, nr 6 (1.09.2009): 511–14. http://dx.doi.org/10.2174/157017809789124812.
Pełny tekst źródłaSong, Yoon Ju, Jin Sun Choi i Jae In Lee. "An Efficient Synthesis of 1-Alkyl-2-phenyl-4-quinolones from 2-Halobenzoic Acids". Bulletin of the Korean Chemical Society 34, nr 10 (20.10.2013): 3117–20. http://dx.doi.org/10.5012/bkcs.2013.34.10.3117.
Pełny tekst źródłaDubern, Jean-Frédéric, i Stephen P. Diggle. "Quorum sensing by 2-alkyl-4-quinolones in Pseudomonas aeruginosa and other bacterial species". Molecular BioSystems 4, nr 9 (2008): 882. http://dx.doi.org/10.1039/b803796p.
Pełny tekst źródłaNiewerth, Heiko, Klaus Bergander, Siri Ram Chhabra, Paul Williams i Susanne Fetzner. "Synthesis and biotransformation of 2-alkyl-4(1H)-quinolones by recombinant Pseudomonas putida KT2440". Applied Microbiology and Biotechnology 91, nr 5 (14.06.2011): 1399–408. http://dx.doi.org/10.1007/s00253-011-3378-0.
Pełny tekst źródłaLi, Dandan, Naoya Oku, Atsumi Hasada, Masafumi Shimizu i 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 (14.06.2018): 1446–51. http://dx.doi.org/10.3762/bjoc.14.122.
Pełny tekst źródłaRitzmann, Niklas H., Almuth Mährlein, Simon Ernst, Ulrich Hennecke, Steffen L. Drees i Susanne Fetzner. "Bromination of alkyl quinolones by Microbulbifer sp. HZ11, a marine Gammaproteobacterium, modulates their antibacterial activity". Environmental Microbiology 21, nr 7 (6.06.2019): 2595–609. http://dx.doi.org/10.1111/1462-2920.14654.
Pełny tekst źródłaUkrainets, I. V., S. G. Taran, O. A. Evtifeeva, O. V. Gorokhova, P. A. Bezuglyi, A. V. Turov, L. N. Voronina i N. I. Filimonova. "4-Hydroxy-2-quinolones 19. A new synthesis of 3-Alkyl-2-oxo-4-hydroxyquinolines". Chemistry of Heterocyclic Compounds 30, nr 5 (maj 1994): 591–95. http://dx.doi.org/10.1007/bf01169841.
Pełny tekst źródłaSáenz, Fabián E., Alexis N. LaCrue, R. Matthew Cross, Jordany R. Maignan, Kenneth O. Udenze, Roman Manetsch i 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, nr 12 (30.09.2013): 6187–95. http://dx.doi.org/10.1128/aac.00492-13.
Pełny tekst źródłaBarr, H., A. Fogarty, N. Halliday, A. Knox, B. Quon, D. Forrester, P. Williams, D. Barrett i M. Camara. "P92 Systemic alkyl quinolones as novel biomarkers for pulmonary exacerbations in cystic fibrosis: a validation study". Thorax 71, Suppl 3 (15.11.2016): A133.2—A134. http://dx.doi.org/10.1136/thoraxjnl-2016-209333.235.
Pełny tekst źródłaXu, Bin, Jun Shao, Xiaomei Huang, Xiaohu Hong i Bingxin Liu. "Synthesis of N-Alkyl-Substituted 4-Quinolones via Tandem Alkenyl and Aryl C-N Bond Formation". Synthesis 44, nr 12 (3.04.2012): 1798–805. http://dx.doi.org/10.1055/s-0031-1290775.
Pełny tekst źródłaLi, Jianye, Weiwei Sun, Muhammad Saalim, Guixiang Wei, Diana A. Zaleta-Pinet i Benjamin R. Clark. "Isolation of 2-Alkyl-4-quinolones with Unusual Side Chains from a Chinese Pseudomonas aeruginosa Isolate". Journal of Natural Products 83, nr 7 (30.06.2020): 2294–98. http://dx.doi.org/10.1021/acs.jnatprod.0c00026.
Pełny tekst źródłaLegendre, Claire, F. Jerry Reen, Marlies J. Mooij, Gerard P. McGlacken, Claire Adams i Fergal O'Gara. "Pseudomonas aeruginosa Alkyl Quinolones Repress Hypoxia-Inducible Factor 1 (HIF-1) Signaling through HIF-1α Degradation". Infection and Immunity 80, nr 11 (4.09.2012): 3985–92. http://dx.doi.org/10.1128/iai.00554-12.
Pełny tekst źródłaPistorius, Dominik, Angelika Ullrich, Simon Lucas, Rolf W. Hartmann, Uli Kazmaier i Rolf Müller. "Biosynthesis of 2-Alkyl-4(1H)-Quinolones in Pseudomonas aeruginosa: Potential for Therapeutic Interference with Pathogenicity". ChemBioChem 12, nr 6 (18.03.2011): 850–53. http://dx.doi.org/10.1002/cbic.201100014.
Pełny tekst źródłaShui, Hongling, Yuhong Zhong, Renshi Luo, Zhanyi Zhang, Jiuzhong Huang, Ping Yang i 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 (27.10.2022): 1507–17. http://dx.doi.org/10.3762/bjoc.18.159.
Pełny tekst źródłaBarr, Helen L., Nigel Halliday, David A. Barrett, Paul Williams, Douglas L. Forrester, Daniel Peckham, Kate Williams i in. "Diagnostic and prognostic significance of systemic alkyl quinolones for P. aeruginosa in cystic fibrosis: A longitudinal study". Journal of Cystic Fibrosis 16, nr 2 (marzec 2017): 230–38. http://dx.doi.org/10.1016/j.jcf.2016.10.005.
Pełny tekst źródłaSong, Yoon Ju, Jin Sun Choi i Jae In Lee. "ChemInform Abstract: An Efficient Synthesis of 1-Alkyl-2-phenyl-4-quinolones (VII) from 2-Halobenzoic Acids." ChemInform 45, nr 9 (14.02.2014): no. http://dx.doi.org/10.1002/chin.201409173.
Pełny tekst źródłaWube, Abraham, Juan-David Guzman, Antje Hüfner, Christina Hochfellner, Martina Blunder, Rudolf Bauer, Simon Gibbons, Sanjib Bhakta i Franz Bucar. "Synthesis and Antibacterial Evaluation of a New Series of N-Alkyl-2-alkynyl/(E)-alkenyl-4-(1H)-quinolones". Molecules 17, nr 7 (9.07.2012): 8217–40. http://dx.doi.org/10.3390/molecules17078217.
Pełny tekst źródłaShao, Jun, Xiaomei Huang, Xiaohu Hong, Bingxin Liu i Bin Xu. "ChemInform Abstract: Synthesis of N-Alkyl-Substituted 4-Quinolones via Tandem Alkenyl and Aryl C-N Bond Formation." ChemInform 43, nr 41 (13.09.2012): no. http://dx.doi.org/10.1002/chin.201241156.
Pełny tekst źródłaRampioni, Giordano, Marilena Falcone, Stephan Heeb, Emanuela Frangipani, Matthew P. Fletcher, Jean-Frédéric Dubern, Paolo Visca, Livia Leoni, Miguel Cámara i Paul Williams. "Unravelling the Genome-Wide Contributions of Specific 2-Alkyl-4-Quinolones and PqsE to Quorum Sensing in Pseudomonas aeruginosa". PLOS Pathogens 12, nr 11 (16.11.2016): e1006029. http://dx.doi.org/10.1371/journal.ppat.1006029.
Pełny tekst źródłaLin, San San, Stefan Kerscher, Ahmad Saleh, Ulrich Brandt, Uwe Groß i 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, nr 11 (listopad 2008): 1455–62. http://dx.doi.org/10.1016/j.bbabio.2008.08.006.
Pełny tekst źródłaBarr, H. L., N. Halliday, D. A. Barrett, P. Williams, D. L. Forrester, D. Peckham, K. Williams i in. "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, nr 6 (listopad 2017): e21. http://dx.doi.org/10.1016/j.jcf.2017.09.008.
Pełny tekst źródłaAyubi, Erfan, Jamal Hallajzadeh i 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, nr 6 (listopad 2017): e19-e20. http://dx.doi.org/10.1016/j.jcf.2017.07.012.
Pełny tekst źródłaUkrainets, L. V., O. V. Gorokhova, S. G. Taran, P. A. Bezulyi, A. V. Turov, N. A. Marusenko i 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, nr 7 (lipiec 1994): 829–36. http://dx.doi.org/10.1007/bf01169641.
Pełny tekst źródłaSeppänen, Otto, Mikko Muuronen i 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, nr 19 (26.05.2014): 4044–52. http://dx.doi.org/10.1002/ejoc.201402224.
Pełny tekst źródłaKilani-Feki, Olfa, Gérald Culioli, Annick Ortalo-Magné, Nabil Zouari, Yves Blache i 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, nr 5 (11.02.2011): 1490–95. http://dx.doi.org/10.1007/s00284-011-9892-6.
Pełny tekst źródłaSciscenko, Iván, Paula García-Negueroles, Ana María Amat, Isabel Oller, Carlos Escudero-Oñate, Laura Ferrando-Climent i Antonio Arques. "Use of Fluorescence Spectroscopy and Chemometrics to Visualise Fluoroquinolones Photodegradation Major Trends: A Confirmation Study with Mass Spectrometry". Molecules 28, nr 2 (12.01.2023): 777. http://dx.doi.org/10.3390/molecules28020777.
Pełny tekst źródłaUkrainets, I. V., N. L. Bereznyakova, V. A. Parshikov i 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, nr 12 (grudzień 2008): 1493–99. http://dx.doi.org/10.1007/s10593-009-0209-7.
Pełny tekst źródłaDow, Lachlan. "How Do Quorum-Sensing Signals Mediate Algae–Bacteria Interactions?" Microorganisms 9, nr 7 (27.06.2021): 1391. http://dx.doi.org/10.3390/microorganisms9071391.
Pełny tekst źródłaSeppaenen, Otto, Mikko Muuronen i 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, nr 8 (luty 2015): no. http://dx.doi.org/10.1002/chin.201508224.
Pełny tekst źródłaUkrainets, I. V., N. L. Bereznyakova, A. A. Davidenko i 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, nr 8 (sierpień 2009): 952–56. http://dx.doi.org/10.1007/s10593-009-0367-7.
Pełny tekst źródłaDepke, Tobias, Janne Gesine Thöming, Adrian Kordes, Susanne Häussler i Mark Brönstrup. "Untargeted LC-MS Metabolomics Differentiates Between Virulent and Avirulent Clinical Strains of Pseudomonas aeruginosa". Biomolecules 10, nr 7 (13.07.2020): 1041. http://dx.doi.org/10.3390/biom10071041.
Pełny tekst źródłaSingh, Shweta, Sharanya Nerella, Srihari Pabbaraja i 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, nr 4 (4.02.2020): 1575–79. http://dx.doi.org/10.1021/acs.orglett.0c00172.
Pełny tekst źródłaUkrainets, I. V., I. A. Tugaibei, N. L. Bereznyakova, V. N. Kravchenko i 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, nr 5 (maj 2008): 565–75. http://dx.doi.org/10.1007/s10593-008-0076-7.
Pełny tekst źródłaUKRAINETS, I. V., O. V. GOROKHOVA, S. G. TARAN, P. A. BEZUGLYI, A. V. TUROV, N. A. MARUSENKO i 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, nr 18 (18.08.2010): no. http://dx.doi.org/10.1002/chin.199518153.
Pełny tekst źródłaNguyen, Angela T., Jace W. Jones, Max A. Ruge, Maureen A. Kane i Amanda G. Oglesby-Sherrouse. "Iron Depletion Enhances Production of Antimicrobials by Pseudomonas aeruginosa". Journal of Bacteriology 197, nr 14 (27.04.2015): 2265–75. http://dx.doi.org/10.1128/jb.00072-15.
Pełny tekst źródłaBrewer, Luke K., Jace W. Jones, Catherine B. Blackwood, Mariette Barbier, Amanda Oglesby-Sherrouse i 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, nr 7 (29.01.2020): 1521–34. http://dx.doi.org/10.1007/s00216-019-02374-0.
Pełny tekst źródłaUkrainets, I. V., L. V. Sidorenko, A. A. Davidenko i 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, nr 4 (sierpień 2010): 445–51. http://dx.doi.org/10.1007/s10593-010-0529-7.
Pełny tekst źródłaUkrainets, I. V., L. V. Sidorenko, A. A. Davidenko i 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, nr 4 (30.12.2010): no. http://dx.doi.org/10.1002/chin.201104152.
Pełny tekst źródłaHuang, Bin, Yaqiu Long, Li-Rui Song, He Li, Shen-Feng Wang i 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.
Pełny tekst źródłaPark, Cheol-Min, Jaehee Bae i Jiyoung Chae. "Synthesis of 2‐Quinolones based on Visible Light‐Catalyzed Annulation of Diazo compounds". Advanced Synthesis & Catalysis, 7.02.2024. http://dx.doi.org/10.1002/adsc.202301220.
Pełny tekst źródła