Gotowa bibliografia na temat „Pyridines”
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Artykuły w czasopismach na temat "Pyridines"
McNally, Andrew, Ryan Dolewski i Michael Hilton. "4-Selective Pyridine Functionalization Reactions via Heterocyclic Phosphonium Salts". Synlett 29, nr 01 (12.12.2017): 08–14. http://dx.doi.org/10.1055/s-0036-1591850.
Pełny tekst źródłaCzarnocki, Zbigniew, i Piotr Pomarański. "Arylpyridines: A Review from Selective Synthesis to Atropisomerism". Synthesis 51, nr 03 (14.12.2018): 587–611. http://dx.doi.org/10.1055/s-0037-1611365.
Pełny tekst źródłaZhang, Li-Juan, Qun Wu, Jing Sun i Chao-Guo Yan. "Synthesis of functionalized spiro[indoline-3,4’-pyridines] and spiro[indoline-3,4’-pyridinones] via one-pot four-component reactions". Beilstein Journal of Organic Chemistry 9 (2.05.2013): 846–51. http://dx.doi.org/10.3762/bjoc.9.97.
Pełny tekst źródłaBrugarolas, P., R. Freifelder, S. H. Cheng i O. DeJesus. "Synthesis of meta-substituted [18F]3-fluoro-4-aminopyridine via direct radiofluorination of pyridine N-oxides". Chemical Communications 52, nr 44 (2016): 7150–52. http://dx.doi.org/10.1039/c6cc02362b.
Pełny tekst źródłaBalkenhohl, Moritz, i Paul Knochel. "Regioselective C–H Activation of Substituted Pyridines and other Azines using Mg- and Zn-TMP-Bases". SynOpen 02, nr 01 (styczeń 2018): 0078–95. http://dx.doi.org/10.1055/s-0036-1591966.
Pełny tekst źródłaMallisetty, Naga Mohan, Hanumantharao Ganipisetti, Debendra Majhi i Venkata Nagendra Kumar Putta. "Design, Synthesis of Some New Scaffolds based on Pyrrolyl-Pyridines as Potential Anticancer Agents". Asian Journal of Chemistry 35, nr 2 (2023): 468–74. http://dx.doi.org/10.14233/ajchem.2023.23974.
Pełny tekst źródłaGad-Elkareem, Mohamed A. M., Azza M. Abdel-Fattah i Mohamed A. A. Elneairy. "Pyrazolo[3,4-b]pyridine in heterocyclic synthesis: synthesis of new pyrazolo[3,4-b]pyridines, imidazo[1',2':1,5]pyrazolo[3,4-b]pyridines, and pyrido[2',3':3,4]pyrazolo[1,5-a]pyrimidines". Canadian Journal of Chemistry 85, nr 9 (1.09.2007): 592–99. http://dx.doi.org/10.1139/v07-089.
Pełny tekst źródłaPreston, Dan, Samantha M. McNeill, James E. M. Lewis, Gregory I. Giles i James D. Crowley. "Enhanced kinetic stability of [Pd2L4]4+ cages through ligand substitution". Dalton Transactions 45, nr 19 (2016): 8050–60. http://dx.doi.org/10.1039/c6dt00133e.
Pełny tekst źródłaBarlin, GB. "Heterocyclic Amplifiers of Phleomycin. VIII. Mono- Bis-(5'-substituted 1',3',4'-thiadiazol-2'-yl)pyridines and Mono(5'-substituted 1',3',4'-thiadiazol-2'-ylmethyl)pyridines". Australian Journal of Chemistry 38, nr 10 (1985): 1491. http://dx.doi.org/10.1071/ch9851491.
Pełny tekst źródłaSchmitt, Martine, Jean-Jacques Bourguignon, Gordon B. Barlin i Les P. Davies. "Imidazo[1,2-b]pyridazines. XXIII Some 5-Deaza Analogues. Syntheses of Some 2-Aryl-6-(chloro, methoxy or unsubstituted)-3- (variously substituted)imidazo[1,2-a]pyridines and Their Affinity for Central and Mitochondrial Benzodiazepine Receptor". Australian Journal of Chemistry 50, nr 7 (1997): 719. http://dx.doi.org/10.1071/c97004.
Pełny tekst źródłaRozprawy doktorskie na temat "Pyridines"
Brice, Heloise. "Dearomatising cyclisations onto pyridines". Thesis, University of Manchester, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.496237.
Pełny tekst źródłaAltuna-Urquijo, M. "New routes to functionalised pyridines". Thesis, Northumbria University, 2005. http://nrl.northumbria.ac.uk/3327/.
Pełny tekst źródłaHarrington, Keith Anthony. "Regioselective synthesis of functionalised pyridines". Thesis, University of Leeds, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.329948.
Pełny tekst źródłaBouteau, Brigitte. "Synthèse et étude physicochimique de pyrrolyl-pyridines, pyrido (2,3-c) pyrrolo (1,2-e) triazépines-1,2,5, triazolo-1,2,4 (4,5-a) pyridines, triazolo (1,2,4) (2,3-a) pyridines". Caen, 1989. http://www.theses.fr/1989CAEN4051.
Pełny tekst źródłaCadu, Alban. "Iridium Catalysed Asymmetric Hydrogenation of Pyridines". Licentiate thesis, Uppsala universitet, Syntetisk organisk kemi, 2013. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-212413.
Pełny tekst źródłaMcConnell, Stuart. "2-functionalised pyridines with transition metals". Thesis, Queen Mary, University of London, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243479.
Pełny tekst źródłaMace, Laura H. "Developing the partial reduction of pyridines". Thesis, University of Oxford, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.398101.
Pełny tekst źródłaGehre, Alexander. "Development of novel routes to pyridines". Thesis, Northumbria University, 2008. http://nrl.northumbria.ac.uk/3533/.
Pełny tekst źródłaChen, Quan. "BF3-mediated direct functionalizations of pyridines". Diss., Ludwig-Maximilians-Universität München, 2014. http://nbn-resolving.de/urn:nbn:de:bvb:19-175551.
Pełny tekst źródłaGalley, Carl Maurice Swedler. "Some chemistry of pyridines and pyridones". Thesis, University of Bristol, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.412833.
Pełny tekst źródłaKsiążki na temat "Pyridines"
Andrews, Ian Philip. Hypervalent iodine oxidations of substituted pyridines. Norwich: University of East Anglia, 1992.
Znajdź pełny tekst źródłaHeo, Christina K. M. Quantitative studies on the addition of pyridines to Michael acceptors. Ottawa: National Library of Canada, 1990.
Znajdź pełny tekst źródłaBanting, Lee. Synthesis and evaluation of perhydroimidazolo [3,4-a] pyridines as fungicides. Portsmouth: Portsmouth Polytechnic, Dept. of Chemistry, 1985.
Znajdź pełny tekst źródłaOmar, Abdirahman Hagi Hassan. Reactions of trihalomethyl derivatives of pyridines and pyrimidines with nucleophiles. Salford: University of Salford, 1986.
Znajdź pełny tekst źródłaUnited States. National Aeronautics and Space Administration., red. Synthesis and characterization of the first main group oxo-centered trinuclear carboxylate: Final report, 1/16/90 to 3/31/94. [Washington, DC: National Aeronautics and Space Administration, 1994.
Znajdź pełny tekst źródłaTrethewey, Andrew Nicholas. Synthesis and evaluation of perhydro-oxazolo [3,4-a] pyridines as fungicides. Portsmouth: Portsmouth Polytechnic, 1985.
Znajdź pełny tekst źródłaV, Auping Judith, Meador Michael A i United States. National Aeronautics and Space Administration., red. Synthesis of substituted 2,3,5,6-tetraarylbenzo(1,2-b:5,4-b')difurans. [Washington, DC: National Aeronautics and Space Administration, 1995.
Znajdź pełny tekst źródłaUnited States. Agency for Toxic Substances and Disease Registry. Division of Toxicology. Pyridine. Atlanta, GA: Division of Toxicology, Dept. of Health and Human Services, Public Health Service, Agency for Toxic Substances Disease Registry, 1992.
Znajdź pełny tekst źródłaG, Bartholini, red. Imidazopyridines in anxiety disorders: A novel experimental and therapeutic approach. New York: Raven Press, 1993.
Znajdź pełny tekst źródłaP, Sauvanet J., Langer S. Z, Morselli Paolo Lucio i Laboratoires d'études et de recherches Synthélabo., red. Imidazopyridines in sleep disorders: A novel experimental and therapeutic approach. New York: Raven Press, 1988.
Znajdź pełny tekst źródłaCzęści książek na temat "Pyridines"
Brown, E. G. "Pyridines". W Ring Nitrogen and Key Biomolecules, 68–87. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-4906-8_4.
Pełny tekst źródłaNewkome, G. R., V. K. Gupta i J. D. Sauer. "Macrocyclic Pyridines". W Chemistry of Heterocyclic Compounds: A Series Of Monographs, 447–633. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186701.ch3.
Pełny tekst źródłaCoutts, R. T., i A. F. Casy. "Pyridines and Reduced Pyridines of Pharmacological Interest". W Chemistry of Heterocyclic Compounds: A Series Of Monographs, 445–524. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186695.ch4.
Pełny tekst źródłaThummel, R. P. "Carbocyclic Annelated Pyridines". W Chemistry of Heterocyclic Compounds: A Series Of Monographs, 253–445. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186701.ch2.
Pełny tekst źródłaShestopalov, Anatoliy M., Lyudmila A. Rodinovskaya, Valeri Yu Mortikov i Alexander E. Fedorov. "Synthesis of Fluorinated Pyridines". W Fluorine in Heterocyclic Chemistry Volume 2, 1–58. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-04435-4_1.
Pełny tekst źródłaLickfeldt, Darin W., Denise P. Cudworth, Daniel D. Loughner i Lowell D. Markley. "Microtubulin Assembly Inhibitors (Pyridines)". W Modern Crop Protection Compounds, 439–45. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527644179.ch10.
Pełny tekst źródłaJoule, J. A., K. Mills i G. F. Smith. "Pyridines: reactions and synthesis". W Heterocyclic Chemistry, 72–119. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-3222-8_5.
Pełny tekst źródłaGonzález-Bello, Concepción, i Luis Castedo. "Six-Membered Heterocycles: Pyridines". W Modern Heterocyclic Chemistry, 1431–525. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527637737.ch16.
Pełny tekst źródłaLickfeldt, Darin W., Denise P. Cudworth, Daniel D. Loughner i Lowell D. Markley. "Microtubulin Assembly Inhibitors (Pyridines)". W Modern Crop Protection Compounds, 493–500. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2019. http://dx.doi.org/10.1002/9783527699261.ch10.
Pełny tekst źródłaLyle, Robert E. "Part B. Partially Reduced Pyridines". W Chemistry of Heterocyclic Compounds: A Series Of Monographs, 137–82. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186633.ch2.
Pełny tekst źródłaStreszczenia konferencji na temat "Pyridines"
Dotsenko, Victor, Darya Lukina i Angela Stolyarova. "Synthesis of new functionalized thieno[2,3-b]pyridines". W The 21st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04853.
Pełny tekst źródłaDotsenko, Victor, i Sergey Krivokolysko. "On the reaction of indole-3-carbaldehyde with cyanothioacetamide: an unexpected approach to indolyl-substituted pyridines and thieno[2,3-b]pyridines". W The 21st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04802.
Pełny tekst źródłaPelosi, André Gasparotto, Leandro H. Zucolotto Cocca, Sandrine Piguel, Leonardo De Boni i Cleber R. Mendonça. "Spectroscopy Study in Styryl Imidazo[4,5-b]Pyridine Derivatives". W Latin America Optics and Photonics Conference. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/laop.2022.m2a.3.
Pełny tekst źródłaMuraviev, V. S., i L. V. Dyaduchenko. "THIENO[2,3-B]PYRIDINES DERIVATIVES AS SOYBEAN PLANT GROWTH REGULATORS". W STATE AND DEVELOPMENT PROSPECTS OF AGRIBUSINESS Volume 2. DSTU-Print, 2020. http://dx.doi.org/10.23947/interagro.2020.2.683-686.
Pełny tekst źródłaValverde, J. V. P., A. G. Pelosi, L. H. Z. Cocca, O. D. Marbello, S. Piguel, L. de Boni i C. R. Mendonça. "Study of Two-Photon Absorption in Imidazo[1,2-a]Pyridines Derivatives". W Latin America Optics and Photonics Conference. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/laop.2022.tu4a.57.
Pełny tekst źródłaKneeteman, Maria. "Nitro-pyridines as Dienophiles in Polar Diels-alder Reactions. A DFT Theoretical Study". W The 16th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2012. http://dx.doi.org/10.3390/ecsoc-16-01086.
Pełny tekst źródłaТрофимов, Б., B. Trofimov, Н. Гусарова i N. Gusarova. "The development of original methodologies of directed synthesis of le-Carbs their analogs and precursors base donacetylene and its derivatives". W Topical issues of translational medicine: a collection of articles dedicated to the 5th anniversary of the day The creation of a department for biomedical research and technology of the Irkutsk Scientific Center Siberian Branch of RAS. Москва: INFRA-M Academic Publishing LLC., 2017. http://dx.doi.org/10.12737/conferencearticle_58be81ec92d17.
Pełny tekst źródłaSharma, R. "The study of dielectric response in binary mixtures of dimethyl substituted pyridines at microwave frequency". W Proceedings of 2005 International Symposium on Electrical Insulating Materials, 2005. (ISEIM 2005). IEEE, 2005. http://dx.doi.org/10.1109/iseim.2005.193330.
Pełny tekst źródłaDucray, Richard, Iain Simpson, Clifford D. Jones, Jon Curwen, Catherine B. Trigwell, Margaret H. Veldman-Jones, Martina Fitzek i in. "Abstract B238: Novel imidazo[1,2-a]pyridines as inhibitors of the IGF-1R tyrosine kinase." W Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Nov 12-16, 2011; San Francisco, CA. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1535-7163.targ-11-b238.
Pełny tekst źródłaVanden Eynde, Jean Jacques, Térence Honoré, Annie Mayence i Tien Huang. "Identification of a Hit in a Small Library of Potential Antiplasmodial Imidazo[4,5-b]pyridines". W 1st International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2015. http://dx.doi.org/10.3390/ecmc-1-a034.
Pełny tekst źródłaRaporty organizacyjne na temat "Pyridines"
Lowe-Ma, Charlotte K., Robin A. Nissan i William S. Wilson. Tetrazolo(1,5-A)pyridines and Furazano(4,5-B)pyridine-1-oxides as Energetic Materials. Fort Belvoir, VA: Defense Technical Information Center, kwiecień 1989. http://dx.doi.org/10.21236/ada209357.
Pełny tekst źródłaKhasaeva, Fatima, Igor Parshikov i Evgeny Zaraisky. Degradation of 2,6-dimethylpyridine by Arthrobacter crystallopoietes. Intellectual Archive, grudzień 2020. http://dx.doi.org/10.32370/iaj.2463.
Pełny tekst źródłaHellier, Paul C., Jerald S. Bradshaw i Reed M. Izatt. Synthesis of Chiral Pyridine-Based Macrobicyclic Clefts. Fort Belvoir, VA: Defense Technical Information Center, maj 1996. http://dx.doi.org/10.21236/ada309257.
Pełny tekst źródłaAuburn, P. R., E. S. Dodsworth, M. A. Haga, W. Liu i W. A. Nevin. Bis(Dioxolene)Bis(Pyridine)Ruthenium Redox Series. Fort Belvoir, VA: Defense Technical Information Center, sierpień 1991. http://dx.doi.org/10.21236/ada240290.
Pełny tekst źródłaEssington, M., i B. Hart. Adsorption of pyridine by combusted oil shale. Office of Scientific and Technical Information (OSTI), marzec 1990. http://dx.doi.org/10.2172/6346070.
Pełny tekst źródłaBlatchford, J. W., S. W. Jessen, L. B. Lin, T. L. Gustafson i A. J. Epstein. Photoluminescence in Pyridine-Based Polymers: Role of Aggregates. Fort Belvoir, VA: Defense Technical Information Center, wrzesień 1997. http://dx.doi.org/10.21236/ada330183.
Pełny tekst źródłaParshikov, Igor. Microbial Transformation of Some Ethylpyridines by Fungi. Intellectual Archive, styczeń 2022. http://dx.doi.org/10.32370/iaj.2635.
Pełny tekst źródłaStolberg, L., J. Lipkowski i D. E. Irish. Adsorption of Pyridine at the Au(311) - Solution Interface. Fort Belvoir, VA: Defense Technical Information Center, luty 1991. http://dx.doi.org/10.21236/ada232823.
Pełny tekst źródłaMudge, Christopher, Bradley Sartain, Benjamin Sperry i Kurt Getsinger. Efficacy of florpyrauxifen-benzyl for eurasian watermilfoil control and nontarget Illinois pondweed, elodea, and coontail response. Engineer Research and Development Center (U.S.), wrzesień 2021. http://dx.doi.org/10.21079/11681/42063.
Pełny tekst źródłaEpstein, A. J., Y. Z. Wang, S. W. Jessen, J. W. Blatchford i D. D. Gebler. Pyridine-Based Conjugated Polymers: Photophysical Properties and Light- Emitting Diodes. Fort Belvoir, VA: Defense Technical Information Center, wrzesień 1997. http://dx.doi.org/10.21236/ada330192.
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