Добірка наукової літератури з теми "Para-substituted"
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Статті в журналах з теми "Para-substituted"
Kozlov, O. F., A. G. Yurchenko, S. D. Isaev, N. A. Leont'eva, and A. V. Nabokova. "Para-adamantyl-substituted phenylpyrazolones." Pharmaceutical Chemistry Journal 20, no. 6 (June 1986): 412–14. http://dx.doi.org/10.1007/bf00758337.
Повний текст джерелаLangle, Sandrine, Franck David-Quillot, Mohamed Abarbri, and Alain Duchêne. "Synthesis of para-substituted styrenes." Tetrahedron Letters 44, no. 8 (February 2003): 1647–49. http://dx.doi.org/10.1016/s0040-4039(03)00027-3.
Повний текст джерелаMansour, El Sayed M. E., Samir K. El-Sadany, Ahmed A. Kassem, and Hamdy A. Maksoud. "Aminolysis of para-substituted benzalacetophenones." Journal of Chemical & Engineering Data 34, no. 3 (July 1989): 368–70. http://dx.doi.org/10.1021/je00057a030.
Повний текст джерелаŠtekláč, Marek, and Martin Breza. "DFT Studies of Substituted Phenols Cytotoxicity I. Para ‐substituted Phenols." ChemistrySelect 6, no. 28 (July 21, 2021): 7049–55. http://dx.doi.org/10.1002/slct.202101568.
Повний текст джерелаIto, Yoshikatsu, Nobuhiro Kawatsuki, Brij Pal Giri, Masahiro Yoshida, and Teruo Matsuura. "Photochemistry of meta-substituted and para-substituted aromatic polycarbonyl compounds." Journal of Organic Chemistry 50, no. 16 (August 1985): 2893–904. http://dx.doi.org/10.1021/jo00216a018.
Повний текст джерелаCihaner, Atilla, and Ahmet M. Önal. "Electrochemical Polymerization of Para‐Substituted Haloanilines." Journal of Macromolecular Science, Part A 43, no. 1 (January 2006): 153–63. http://dx.doi.org/10.1080/10601320500406032.
Повний текст джерелаZuev, Vjacheslav V., Fabio Bertini, and Guido Audisio. "Thermal degradation of para-substituted polystyrenes." Polymer Degradation and Stability 71, no. 2 (January 2001): 213–21. http://dx.doi.org/10.1016/s0141-3910(00)00113-0.
Повний текст джерелаLangle, Sandrine, Franck David-Quillot, Alexia Balland, Mohamed Abarbri, and Alain Duchêne. "General access to para-substituted styrenes." Journal of Organometallic Chemistry 671, no. 1-2 (April 2003): 113–19. http://dx.doi.org/10.1016/s0022-328x(03)00053-6.
Повний текст джерелаDouarre, L., R. Arnaud, J. Lemaire, A. Deflandre, and H. Richard. "Photochemical study of para-substituted anilines." Journal of Photochemistry and Photobiology A: Chemistry 87, no. 2 (March 1995): 143–50. http://dx.doi.org/10.1016/1010-6030(94)03978-4.
Повний текст джерелаWu, Biqi, and Harry S. Mosher. "Configuration of some para-substituted benzhydrols." Journal of Organic Chemistry 51, no. 10 (May 1986): 1904–6. http://dx.doi.org/10.1021/jo00360a049.
Повний текст джерелаДисертації з теми "Para-substituted"
Srichan, Sansanee. "Synthesis of sequence-controlled polymers by copolymerization of para-substituted styrenic derivatives and N-substituted maleimides." Thesis, Strasbourg, 2015. http://www.theses.fr/2015STRAF005/document.
Повний текст джерелаIn this work, controlled radical copolymerizations of donor (styrenic derivatives) and acceptor monomers (N-substituted maleimides, MIs) have been investigated in order to synthesize sequence-controlled polymers. These macromolecules were prepared by nitroxide mediated polymerization using the nitroxide SG1 as a control agent. Polymers with defined microstructures were obtained by time-controlled addition of small amounts of acceptor monomers during the polymerization of a large excess of donor monomer. In this thesis, new styrenic derivatives have been studied in order to design sequence-controlled polymers with functional backbones. For example, sequence-controlled polyelectrolytes based on poly(4-hydroxystyrene)s and poly(vinyl benzyl amine)s were obtained through the polymerization of protected styrenic derivatives (i.e. 4-tert-butoxystyrene, 4-acetoxystyrene and N-(p-vinyl benzyl)phthalimide) with non-stoichiometric quantities of N-substituted maleimides. Furthermore, the preparation of PEGylated biocompatible water-soluble polymers was also investigated. Sequence-controlled polymers bearing protected alkyne functional groups on each styrene units were first synthesized followed by the removal of their protecting groups allowing the grafting of α-methoxy-ω-azido-PEG on free alkyne moieties via CuAAC mediated click reaction. Finally, sequence-controlled semi-crystalline polymers were synthesized using octadecylstyrene as a donor monomer. The thermal properties of these polymers were studied to evaluate the influence of polymer microstructure on crystallization behavior
Ramlall, Pratima Madhuri. "Photogeneration of nitrenium ions of para-substituted phenyl azides by laser flash photolysis." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape7/PQDD_0002/NQ41284.pdf.
Повний текст джерелаRautenbach, Daniel. "The development of an electrochemical process for the production of para-substituted di-hydroxy benzenes." Thesis, Nelson Mandela Metropolitan University, 2005. http://hdl.handle.net/10948/159.
Повний текст джерелаGalvis, Pareja David Andrés. "Pharmacological evaluation of new meta- and para-hydroxyl substituted C-4-aryl-1,4-dihydropyridines in cardiomyocytes." Tesis, Universidad de Chile, 2011. http://www.repositorio.uchile.cl/handle/2250/105211.
Повний текст джерелаBonano, Julie S. "Structural Determinants of Abuse-Related Neurochemical and Behavioral Effects of Para-Substituted Methcathinone Analogs in Rats." VCU Scholars Compass, 2015. http://scholarscompass.vcu.edu/etd/3911.
Повний текст джерелаZhu, Peizhi, and 朱沛志. "Time-resolved resonance Raman and density functional theory studies ofselected para-phenyl substituted arylnitrenium ions and arylnitrenes." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2003. http://hub.hku.hk/bib/B31246370.
Повний текст джерелаSchäfer, Julian [Verfasser], and Christoph [Gutachter] Lambert. "Synthesis and Photophysical Investigation of Donor-Acceptor-Substituted meta- and para-Benzene Derivatives / Julian Schäfer ; Gutachter: Christoph Lambert." Würzburg : Universität Würzburg, 2018. http://d-nb.info/1171132948/34.
Повний текст джерелаChan, Pik-ying, and 陳碧瑩. "Time-resolved resonance Raman investigation of selected para-substituted phenylnitrenium ions and the 2-fluorenylnitrenium ionreaction with guanosine." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2005. http://hub.hku.hk/bib/B36189881.
Повний текст джерелаHickman, Hazel Alice. "Towards the synthesis of alkoxy-substituted [2.2]para-cyclophenes and [2.2]para-cyclophane-1-enes : tailored monomers for the preparation of well-defined, functionalised PPV." Thesis, University of Leicester, 2005. http://hdl.handle.net/2381/30100.
Повний текст джерелаChan, Pik-ying. "Time-resolved resonance Raman investigation of selected para-substituted phenylnitrenium ions and the 2-fluorenylnitrenium ion reaction with guanosine." Click to view the E-thesis via HKUTO, 2005. http://sunzi.lib.hku.hk/hkuto/record/B36189881.
Повний текст джерелаКниги з теми "Para-substituted"
Genus, Devon. Biological synthesis of chemical and materials: Production of substituted para-polyphenylene. Lowell, Mass: Toxics Use Reduction Institute, University of Massachusetts Lowell, 1992.
Знайти повний текст джерелаKoerner, Terry. Using kinetic isotope effects to model the transition states for the sn2 reactions between sodium borohydride and para-substituted benzyl chlorides. Sudbury, Ont: Laurentian University Press, 1996.
Знайти повний текст джерелаRamlall, Pratima Madhuri. Photogeneration of nitrenium ions of para-substituted phenyl azides by laser flash photolysis. 1999.
Знайти повний текст джерелаЧастини книг з теми "Para-substituted"
Schultz, T. Wayne, Geoffrey W. Riggin, and Sonji K. Wesley. "Structure-Activity Relationships for Para-Substituted Phenols." In QSAR in Environmental Toxicology - II, 333–45. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3937-0_25.
Повний текст джерелаBiava, M., R. Fioravanti, G. C. Porretta, L. Caruso, G. Musumarra, N. Simonetti, and A. Villa. "CARSO response surface modelling of para-substituted -N-heteroaryl benzylamines antimycotic activities." In Trends in QSAR and Molecular Modelling 92, 319–20. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1472-1_61.
Повний текст джерелаHehre, W. J., R. W. Taft, and R. D. Topsom. "Ab Initio Calculations of Charge Distributions in Monosubstituted Benzenes and in Meta- and Para-Substituted Fluorobenzenes. Comparison with 1 H, 13 C, and 19 F Nmr Substituent Shifts." In Progress in Physical Organic Chemistry, 159–87. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470171912.ch6.
Повний текст джерелаMark, James E., Dale W. Schaefer, and Gui Lin. "Types of Polysiloxanes." In The Polysiloxanes. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780195181739.003.0005.
Повний текст джерела"Para-substituted Aniline Hydrogenation Over Rhodium Catalysts: Metal Crystallite Size and Catalyst Pore Size Effects Department of Chemistry, The University, Glasgow G12 8QQ, Scotland, U.K." In Catalysis of Organic Reactions, 101–8. CRC Press, 2005. http://dx.doi.org/10.1201/9781420028034-19.
Повний текст джерелаMark, James E., Harry R. Allcock, and Robert West. "Polysiloxanes and Related Polymers." In Inorganic Polymers. Oxford University Press, 2005. http://dx.doi.org/10.1093/oso/9780195131192.003.0008.
Повний текст джерелаMark, James E., Dale W. Schaefer, and Gui Lin. "Introduction." In The Polysiloxanes. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780195181739.003.0003.
Повний текст джерелаSridhar, Rapolu, D. Ravinder, J. Laxman Naik, K. Vijaya Kumar, N. Maramu, and S. Katlakunta. "Investigation of Structural, Magnetic and Electrical Properties of Chromium Substituted Nickel Ceramic Nanopowders." In Advanced Ceramic Materials. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.94941.
Повний текст джерелаТези доповідей конференцій з теми "Para-substituted"
Thiemann, Thies, Nuha al Soom, and Saber Elsuccary. "Preparation of methoxy-substituted para-benzoquinones." In The 20th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a007.
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 джерелаBedre, L. K., and B. M. Bahirwar. "Synthesis and optical study of ortho, meta and para methoxy substituted 2, 4–diphenyl quinoline." In INTERNATIONAL CONFERENCE ON “MULTIDIMENSIONAL ROLE OF BASIC SCIENCE IN ADVANCED TECHNOLOGY” ICMBAT 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5100486.
Повний текст джерелаReddy, B. Venkatram, Jai Kishan Ojha, G. Ramana Rao, P. Predeep, Mrinal Thakur, and M. K. Ravi Varma. "Vibrational Analysis of Some Substituted Methylbenzenes Part II. Transferability of Force Constants—The Case of Tetra-, Tri-methylbenzenes and Nitro-para-toluidine." In OPTICS: PHENOMENA, MATERIALS, DEVICES, AND CHARACTERIZATION: OPTICS 2011: International Conference on Light. AIP, 2011. http://dx.doi.org/10.1063/1.3643583.
Повний текст джерелаPrimozic, Ines, Marijana Bolant, Alma Ramic, and Srdjanka Tomic. "Preparation of novel meta and para substituted N-benzyl protected quinuclidine esters and their resolution with butyrylcholinesterase." In The 15th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2011. http://dx.doi.org/10.3390/ecsoc-15-00740.
Повний текст джерелаЗвіти організацій з теми "Para-substituted"
Barney, James R. A Theoretical Study of Conjugation in Para-Substituted Nitrobenzenes. Fort Belvoir, VA: Defense Technical Information Center, May 1990. http://dx.doi.org/10.21236/ada227167.
Повний текст джерела