Добірка наукової літератури з теми "N - Aryl Y - Lactam"
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Статті в журналах з теми "N - Aryl Y - Lactam"
Tsang, Wing Y., Naveed Ahmed, Karl Hemming та Michael I. Page. "Competitive endo- and exo-cyclic CN fission in the hydrolysis of N-aroyl β-lactams". Canadian Journal of Chemistry 83, № 9 (1 вересня 2005): 1432–39. http://dx.doi.org/10.1139/v05-153.
Повний текст джерелаBarba, Victor, Cecilia Hernández, Susana Rojas-Lima, Norberto Farfán та Rosa Santillan. "Preparation of N-aryl-substituted spiro-β-lactams via Staudinger cycloaddition". Canadian Journal of Chemistry 77, № 12 (5 грудня 1999): 2025–32. http://dx.doi.org/10.1139/v99-212.
Повний текст джерелаMöhrle, H., and M. Jeandrée. "Chinazolinderivate durch Cyclodehydrierung von N-(2-substituierten Aryl)-Piperidinen / Quinazoline Derivatives by Cyclodehydrogenation of N-(2-Substituted Aryl)-Piperidines." Zeitschrift für Naturforschung B 54, no. 12 (December 1, 1999): 1577–88. http://dx.doi.org/10.1515/znb-1999-1217.
Повний текст джерелаFang, Zeguo, Lin Xie, Liang Wang, Qian Zhang та Dong Li. "Silver-catalyzed cascade cyclization and functionalization of N-aryl-4-pentenamides: an efficient route to γ-lactam-substituted quinone derivatives". RSC Advances 12, № 41 (2022): 26776–80. http://dx.doi.org/10.1039/d2ra05283k.
Повний текст джерелаSaliu, Francesco, Marco Orlandi, and Maurizio Bruschi. "N-Aryl Lactams by Regioselective Ozonation of N-Aryl Cyclic Amines." ISRN Organic Chemistry 2012 (October 15, 2012): 1–5. http://dx.doi.org/10.5402/2012/281642.
Повний текст джерелаHaldar, Pranab, та Jayanta K. Ray. "CAN mediated decarboxylative hydroxylation/alkoxylation of N-aryl-γ-lactam-carboxylic acids at room temperature: an easy access to N-aryl-α-hydroxy/alkoxy-γ-lactams". Tetrahedron Letters 49, № 22 (травень 2008): 3659–62. http://dx.doi.org/10.1016/j.tetlet.2008.03.147.
Повний текст джерелаYurino, Taiga, Takeshi Ohkuma, Hamdiye Ece, and Yuji Tange. "Silyl Cyanopalladate-Catalyzed Friedel–Crafts-Type Cyclization Affording 3-Aryloxindole Derivatives." Synlett 32, no. 09 (January 26, 2021): 935–39. http://dx.doi.org/10.1055/a-1373-7017.
Повний текст джерелаPatra, Prasanta, Gandhi K. Kar, Aparna Sarkar, Jayanta K. Ray, Tista Dasgupta, Mahua Ghosh та Sugata Bhattacharya. "N-Aryl Modification in γ-Lactam: Design and Synthesis of Novel Monocyclic γ-Lactam Derivatives as Inhibitor for Bacterial Propagation". Synthetic Communications 42, № 20 (21 червня 2012): 3031–41. http://dx.doi.org/10.1080/00397911.2011.574807.
Повний текст джерелаDorbec, Matthieu, Jean-Claude Florent, Claude Monneret, Marie-Noëlle Rager та Emmanuel Bertounesque. "1-Aryltetralin privileged structure-based libraries: parallel synthesis of N-aryl and N-biaryl γ-lactam lignans". Tetrahedron 62, № 50 (грудень 2006): 11766–81. http://dx.doi.org/10.1016/j.tet.2006.09.026.
Повний текст джерелаPatra, Prasanta, Gandhi K. Kar, Aparna Sarkar, Jayanta K. Ray, Tista Dasgupta, Mahua Ghosh та Sugata Bhattacharya. "ChemInform Abstract: N-Aryl Modification in γ-Lactam: Design and Synthesis of Novel Monocyclic γ-Lactam Derivatives as Inhibitor for Bacterial Propagation." ChemInform 44, № 1 (1 січня 2013): no. http://dx.doi.org/10.1002/chin.201301160.
Повний текст джерелаДисертації з теми "N - Aryl Y - Lactam"
Barman, Gopa. "Synthetic studies on N - Aryl Y - Lactam & N - Aryl Y - Thio - Lactam : chemoselective Transformation to N-Aryl-Pyrrolidine, N-Aryl Succinimide and Other Bioactive Compounds." Thesis, University of North Bengal, 2009. http://hdl.handle.net/123456789/1379.
Повний текст джерелаBhattacharya, Biplob. "Synthesis and Anti-MRSA Activity of Hydrophilic C3-Acylated N-Thiolated β-Lactams and N-Acyl Ciprofloxacin-N-Thiolated β-Lactam Hybrids". Scholar Commons, 2012. http://scholarcommons.usf.edu/etd/4289.
Повний текст джерелаBekdemir, Yunus. "The mechanisms of hydrolysis and protonation behaviour of N-aryl sultams." Thesis, University of Essex, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.387004.
Повний текст джерелаDyke, Alan. "Novel Câ‚‚-symmetric N,N-donor ligands and the anionic thia-Fries rearrangement of aryl triflates." Thesis, University of Bristol, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.404435.
Повний текст джерелаYasui, Hiroto. "Studies on Addition to 1-Aryl-1-alkynes and N-Alkynyl Amides." 京都大学 (Kyoto University), 2008. http://hdl.handle.net/2433/57271.
Повний текст джерела0048
新制・課程博士
博士(工学)
甲第13827号
工博第2931号
新制||工||1433(附属図書館)
26043
UT51-2008-C743
京都大学大学院工学研究科材料化学専攻
(主査)教授 大嶌 幸一郎, 教授 檜山 爲次郎, 教授 松原 誠二郎
学位規則第4条第1項該当
Mori, Shigeki. "Studies on metallation of meso-aryl substituted hexaphyrins and N-fused pentaphyrins." 京都大学 (Kyoto University), 2008. http://hdl.handle.net/2433/136922.
Повний текст джерелаBaeza, Mario Ivan. "Synthesis and characterization of acetylenic derivatives of the actinide extractant (aryl)-N,N-di-(alkyl)carbamoylmethylphosphine oxide (CMPO)." To access this resource online via ProQuest Dissertations and Theses @ UTEP, 2008. http://0-proquest.umi.com.lib.utep.edu/login?COPT=REJTPTU0YmImSU5UPTAmVkVSPTI=&clientId=2515.
Повний текст джерелаProsen, Katherine Rose. "Investigating the Mode of Action of a Novel N-sec-butylthiolated Beta-lactam Against Staphylococcus aureus." Scholar Commons, 2010. http://scholarcommons.usf.edu/etd/3609.
Повний текст джерелаCui, Xiuhua. "Asymmetric hydrogenations of aryl alkenes using imidazol-2-ylidene iridium complexes." Texas A&M University, 2005. http://hdl.handle.net/1969.1/2456.
Повний текст джерелаJiao, Dezhi. "Alkyl and aryl imidazolium salts in aqueous supramolecular systems with cucurbit[n]uril." Thesis, University of Cambridge, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.610692.
Повний текст джерелаКниги з теми "N - Aryl Y - Lactam"
Henderson, Colin M. Nucleophilic additions to C-aryl, N-arylsulphonyl methyleneimines. [S.l: The Author], 1992.
Знайти повний текст джерелаIkhlef, Fatima. Routes to 4-aryl-1-N-methylanilinobut-3-en-2-ones and reactions of 2-phenylethylamine. Salford: University of Salford, 1985.
Знайти повний текст джерелаInternational Conference on Carcinogenic and Mutagenic N-Substituted Aryl Compounds (3rd 1987 Dearborn, Mich.). Carcinogenic and mutagenic responses to aromatic amines and nitroarenes: Proceedings of the Third International Conference on Carcinogenic and Mutagenic N-Substituted Aryl Compounds, held April 25-28, 1987, in Dearborn Michigan. Edited by King Charles M. 1932-, Romano Louis James 1950-, and Schuetzle Dennis 1942-. New York: Elsevier, 1988.
Знайти повний текст джерелаCarcinogenic and mutagenic N-substituted aryl compounds. [Research Triangle Park, NC]: National Institutes of Health, National Institute of Environmental Health Sciences, 1994.
Знайти повний текст джерелаLagerman, Robert K. Metal ion induced decomposition of N-Aryl-O-pivaloylhydroxylamines in aqueous solution. 1989.
Знайти повний текст джерелаЧастини книг з теми "N - Aryl Y - Lactam"
Atwood, David A. "(IV) into N-C (Aryl) Bonds." In Inorganic Reactions and Methods, 160. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145296.ch145.
Повний текст джерелаMitchell, Glynn, Nigel J. Barnes, John M. Cox, Ian R. Matthews, David R. Parry, David P. J. Pearson, and Stephen C. Smith. "Synthesis and Structure-Activity Relationships in a Novel Class ofN-Aryl Lactam Herbicides." In ACS Symposium Series, 18–29. Washington, DC: American Chemical Society, 2001. http://dx.doi.org/10.1021/bk-2002-0800.ch003.
Повний текст джерелаMonnier, Florian, and Marc Taillefer. "Copper-Catalyzed C(aryl)–N Bond Formation." In Amination and Formation of sp2 C-N Bonds, 173–204. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/3418_2013_69.
Повний текст джерелаKawada, Kosuke. "N-Fluoropyridinium Salt Fluorination for Preparing Aryl Fluorides." In Fluorination, 1–14. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-1855-8_40-1.
Повний текст джерелаKawada, Kosuke. "N-Fluoropyridinium Salt Fluorination for Preparing Aryl Fluorides." In Fluorination, 1–14. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-10-1855-8_40-2.
Повний текст джерелаKawada, Kosuke. "N-Fluoropyridinium Salt Fluorination for Preparing Aryl Fluorides." In Fluorination, 324–38. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-10-3896-9_40.
Повний текст джерелаDöpp, D., A. A. Hassan, A. M. Nour-el-Din, and A. E. Mourad. "A Novel Reaction of Tetracyanoethylene with N-Aryl-Isoindolines." In Organic Free Radicals, 41–42. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73963-7_21.
Повний текст джерелаNielsen, David J., and Kingsley J. Cavell. "Pd-NHC Complexes as Catalysts in Telomerization and Aryl Amination Reactions." In N-Heterocyclic Carbenes in Synthesis, 73–102. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/9783527609451.ch4.
Повний текст джерелаJuliano, Luiz, Maria Helena S. Cezari, and Regina S. H. Carvalho. "Studies on lactam formation during the coupling procedures with N α-carbobenzoxy-N G-tosylarginine." In Peptides 1992, 247–48. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1470-7_99.
Повний текст джерелаBartsch, Richard A., David A. Babb, and Brian E. Knudsen. "Synthesis and Alkali Metal Cation Complexation of N-Aryl [3.2.2] Cryptands." In Inclusion Phenomena in Inorganic, Organic, and Organometallic Hosts, 407–11. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3987-5_67.
Повний текст джерелаТези доповідей конференцій з теми "N - Aryl Y - Lactam"
Liu, Chang, Jing Zhu, Wei Huang, Jin Xu, Changgui Lu, and Yiping Cui. "Quadratic nonlinear optical properties of N-aryl stilbazolium dyes." In Nonlinear Optics: Technologies and Applications. SPIE, 2007. http://dx.doi.org/10.1117/12.757577.
Повний текст джерелаŚcianowski, Jacek, Agata Pacuła, and Magdalena Obieziurska. "N-aryl benzisoselenazolones – synthesis, transformations and antioxidant activity." In The 20th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a019.
Повний текст джерелаKOIKE, R., J. MOTOYOSHIYA, and H. AOYAMA. "THE HIGH ENERGY KEY INTERMEDIATES IN THE PEROXYOXALATE CHEMILUMINESCENCE OF 2,4,6-TRICHLOROPHENYL N-ARYL-N-TOSYLOXAMATES." In Proceedings of the 13th International Symposium. WORLD SCIENTIFIC, 2005. http://dx.doi.org/10.1142/9789812702203_0037.
Повний текст джерелаChaves, Humberto T., Ana M. Lobo, Sundaresan Prabhakar, and Henry S. Rzepa. "A theoretical mechanistic investigation of asymmetric aziridination by N-Aryl-O-acylhydroxylamines." In The first European conference on computational chemistry (E.C.C.C.1). AIP, 1995. http://dx.doi.org/10.1063/1.47868.
Повний текст джерелаPindjakova, Dominika, Lucia Vrablova, Tomas Strharsky, Jiri Kos, and Josef Jampilek. "Investigation of Interactions of ortho- and para-N-Aryl-Substituted 2-Trifluoromethylcinnamanilides." In ECSOC-25. Basel Switzerland: MDPI, 2021. http://dx.doi.org/10.3390/ecsoc-25-11651.
Повний текст джерелаCieślak, Jacek, Jadwiga Jankowska, Michał Sobkowski, Annika Kers, Inger Kers, Jacek Stawinski, and Adam Kraszewski. "The reactions of aryl nucleoside H-phosphonates with O-, N-, and S-nucleophiles." In XIth Symposium on Chemistry of Nucleic Acid Components. Prague: Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 1999. http://dx.doi.org/10.1135/css199902063.
Повний текст джерелаRidzuan, M. S. M., M. Z. Jaafar, and M. M. Zain. "Quantitative structure-activity relationship (QSAR) modelling of N-aryl derivatives as cholinesterase inhibitors." In 2012 IEEE Symposium on Humanities, Science and Engineering Research (SHUSER). IEEE, 2012. http://dx.doi.org/10.1109/shuser.2012.6269006.
Повний текст джерелаGonec, Tomas, Lucia Vrablova, Dominika Pindjakova, Tomas Strharsky, Michal Oravec, and Josef Jampilek. "Preparation and Hydro-Lipophilic Properties of Monosubstituted N-Aryl-4-hydroxyquinoline-3-carboxanilides." In International Electronic Conference on Synthetic Organic Chemistry. Basel Switzerland: MDPI, 2022. http://dx.doi.org/10.3390/ecsoc-26-13548.
Повний текст джерелаKeung Chui, Wai, Anton Dolzhenko, and Hriday Bera. "Synthesis of N-(3(5)-Aryl-1,2,4-triazol-5(3)-yl)-N'-carbethoxythioureas and Their Tautomerism in DMSO Solution." In The 13th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00187.
Повний текст джерелаPalermo, Mark G., Rohan Beckwith, Christopher S. Straub, Kara Herlihy, Yiping Shen, Xiaolu Zhang, Matthew Clapham, and Brian Hurley. "Abstract C54: Aryl-N-(1H-imidazol-2-yl)-acetamides: Nonpeptidic binders of Bir3 cIAP protein." In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Oct 19-23, 2013; Boston, MA. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1535-7163.targ-13-c54.
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