Добірка наукової літератури з теми "Organic groups"
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Статті в журналах з теми "Organic groups"
Yamamoto, Katsutoshi, Yuki Nohara, Yusuke Domon, Yoko Takahashi, Yasuyuki Sakata, Jacques Plévert, and Takashi Tatsumi. "Organic−Inorganic Hybrid Zeolites with Framework Organic Groups." Chemistry of Materials 17, no. 15 (July 2005): 3913–20. http://dx.doi.org/10.1021/cm048367g.
Повний текст джерелаWan, Ying, Dieqing Zhang, Na Hao, and Dongyuan Zhao. "Organic groups functionalised mesoporous silicates." International Journal of Nanotechnology 4, no. 1/2 (2007): 66. http://dx.doi.org/10.1504/ijnt.2007.012316.
Повний текст джерелаHodge, P. "Protective groups in organic synthesis." Polymer 33, no. 16 (January 1992): 3542. http://dx.doi.org/10.1016/0032-3861(92)91123-j.
Повний текст джерелаWilson, A. J. C. "Space groups rare for organic compounds." Acta Crystallographica Section A Foundations of Crystallography 43, a1 (August 12, 1987): C289. http://dx.doi.org/10.1107/s0108767387077717.
Повний текст джерелаDral, A. Petra, and Johan E. ten Elshof. "Organic groups influencing microporosity in organosilicas." Microporous and Mesoporous Materials 267 (September 2018): 267–73. http://dx.doi.org/10.1016/j.micromeso.2018.03.036.
Повний текст джерелаCreyghton, Edward J. "Organic groups cling to the pores." Nature 393, no. 6680 (May 1998): 21–22. http://dx.doi.org/10.1038/29886.
Повний текст джерелаRavikumar, Velayutham, Andrea Fin, Naomi Sakai, and Stefan Matile. "Solubilising groups: a conceptual equivalent of protecting groups in organic synthesis." Supramolecular Chemistry 23, no. 1-2 (August 31, 2010): 69–73. http://dx.doi.org/10.1080/10610278.2010.510193.
Повний текст джерелаSurtiningsih, Tini, Fatimah Fatimah, Ni’matuzahroh Ni’matuzahroh, Agus Supriyanto, and Tri Nurhariyati. "PELATIHAN PEMBUATAN PUPUK ORGANIK CAIR PADA KELOMPOK TANI DI KABUPATEN PROBOLINGGO." Jurnal Layanan Masyarakat (Journal of Public Services) 2, no. 1 (June 10, 2020): 21. http://dx.doi.org/10.20473/jlm.v2i1.2018.21-24.
Повний текст джерелаJarowicki, Krzysztof, and Philip Kocienski. "Protecting groups." Contemporary Organic Synthesis 2, no. 5 (1995): 315. http://dx.doi.org/10.1039/co9950200315.
Повний текст джерелаJarowicki, Krzysztof, and Philip Kocienski. "Protecting groups." Contemporary Organic Synthesis 3, no. 5 (1996): 397. http://dx.doi.org/10.1039/co9960300397.
Повний текст джерелаДисертації з теми "Organic groups"
Dunlop, J. E. "Coordinated leaving groups in organic synthesis." Thesis, Bucks New University, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.374820.
Повний текст джерелаMouselmani, Rim. "Reduction of Organic Functional Groups Using Hypophosphites." Thesis, Lyon, 2018. http://www.theses.fr/2018LYSE1241/document.
Повний текст джерелаRecently, requirements in chemistry are changing fast, since sustainable development has retained more attention. Green chemistry principles have promoted chemists to develop chemical products and processes that reduce or eliminate hazardous substances. The research work described in this thesis is focused on the development of new reducing systems using hypophosphites as substitutes for traditional toxic reducing agents.In order to achieve this goal, aromatic nitriles were reduced into the corresponding aldehydes by the formation of hydrogen gas and nickel nanoparticles upon combining a nickel precursor with calcium hypophosphite in the presence of base in a biphasic medium. Moreover, aromatic nitriles were reduced into primary amines using calcium hypophosphite and the heterogeneous catalyst palladium on carbon. The nature of the metal catalyst, additives, solvents, temperature, and concentrations were studied in details.On the other hand, the well-known direct reductive amination of aliphatic and aromatic ketones was done for the first time using heterogeneous palladium on carbon, and ammonium hypophosphite which acts as a source of ammonia and as a reducing agent at the same time. During optimization different parameters were studied
Nomura, Glenn Sterling. "Derivatives of 4-ketoperhydroazulene with bridgehead methyl groups." Diss., Georgia Institute of Technology, 1985. http://hdl.handle.net/1853/27064.
Повний текст джерелаLee, Duckhee. "The design of organosilyl groups to control organic reactions." Thesis, University of Cambridge, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.624740.
Повний текст джерелаAhmed, K. M. "Diels-Alder reaction of quinones carrying electron-withdrawing groups." Thesis, University of Manchester, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.234154.
Повний текст джерелаHussain, Firasat [Verfasser]. "Hybrid organic-inorganic polyoxometalates functionalized by diorganotin groups / Firasat Hussain." Bremen : IRC-Library, Information Resource Center der Jacobs University Bremen, 2008. http://d-nb.info/1034891162/34.
Повний текст джерелаLongstaff, Peter A. "Novel side chain protecting groups for solid phase peptide synthesis." Thesis, University of Edinburgh, 1989. http://hdl.handle.net/1842/15232.
Повний текст джерелаKorzycka, Karolina Anna. "Two-photon sensitive protecting groups for biological application." Thesis, University of Oxford, 2015. http://ora.ox.ac.uk/objects/uuid:7e895ed2-04a5-4c0b-9105-74461eae8796.
Повний текст джерелаHe, Chaobin. "Synthesis and structure of rigid chain polyamides with bulky side groups." Thesis, University of Cambridge, 1994. https://www.repository.cam.ac.uk/handle/1810/273003.
Повний текст джерелаDeodhar, Bhushan S. "Towards the development of rotaxanes with two functional blocking groups." University of Cincinnati / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1311690891.
Повний текст джерелаКниги з теми "Organic groups"
Protecting groups. 3rd ed. Stuttgart: Georg Thieme, 2004.
Знайти повний текст джерелаProtecting groups. Stuttgart: G. Thieme, 2000.
Знайти повний текст джерелаProtecting groups. Stuttgart: G. Thieme, 1994.
Знайти повний текст джерелаM, Wuts Peter G., ed. Protective groups in organic synthesis. 3rd ed. New York: Wiley, 1999.
Знайти повний текст джерелаMcOmie, J. F. W., ed. Protective Groups in Organic Chemistry. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4684-7218-9.
Повний текст джерелаGreene, Theodora W. Protective groups in organic synthesis. 2nd ed. New York: Wiley, 1991.
Знайти повний текст джерелаWuts, Peter G. M., ed. Greene's Protective Groups in Organic Synthesis. Hoboken, New Jersey: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118905074.
Повний текст джерелаGordon, Hanna J., ed. Quantitative organic analysis via functional groups. 4th ed. Malabar, Fla: R.E. Krieger Pub. Co., 1988.
Знайти повний текст джерелаR, Katritzky Alan, Meth-Cohn Otto, Rees Charles W, and Ley Steven V, eds. Comprehensive organic functional group transformations. Oxford: Pergamon, 1995.
Знайти повний текст джерелаR, Katritzky Alan, Meth-Cohn Otto, Rees Charles W, and Pattenden Gerald, eds. Comprehensive organic functional group transformations. Oxford: Pergamon, 1995.
Знайти повний текст джерелаЧастини книг з теми "Organic groups"
Sarker, Satyajit D., and Lutfun Nahar. "Organic Functional Groups." In Chemistry for Pharmacy Students, 59–189. West Sussex, England: John Wiley & Sons, Ltd,., 2013. http://dx.doi.org/10.1002/9781118687529.ch4.
Повний текст джерелаBoons, G. J. "Protecting Groups." In Organic Synthesis with Carbohydrates, 26–55. Sheffield, UK: Sheffield Academic Press Ltd, 2008. http://dx.doi.org/10.1002/9780470760321.ch2.
Повний текст джерелаGutman, Ivan, and Oskar E. Polansky. "Automorphism Groups." In Mathematical Concepts in Organic Chemistry, 108–16. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-70982-1_10.
Повний текст джерелаGutman, Ivan, and Oskar E. Polansky. "Symmetry Groups." In Mathematical Concepts in Organic Chemistry, 85–107. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-70982-1_9.
Повний текст джерелаBurgess, D. A. "Organic Chemistry — Functional Groups." In Work Out Chemistry ‘A’ Level, 158–68. London: Macmillan Education UK, 1987. http://dx.doi.org/10.1007/978-1-349-24067-8_12.
Повний текст джерелаVančik, Hrvoj. "Functional Groups." In Basic Organic Chemistry for the Life Sciences, 17–20. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-07605-8_2.
Повний текст джерелаVančik, Hrvoj. "Functional Groups." In Basic Organic Chemistry for the Life Sciences, 19–22. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-92438-6_2.
Повний текст джерелаSaunders, K. J. "Other Aromatic Polymers Containing p-Phenylene Groups." In Organic Polymer Chemistry, 265–85. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-1195-6_12.
Повний текст джерелаCarey, Francis A., and Richard J. Sundberg. "Reactions of Carbon Nucleophiles with Carbonyl Groups." In Advanced Organic Chemistry, 55–120. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-9797-7_2.
Повний текст джерелаCarey, Francis A., and Richard J. Sundberg. "Reduction of Carbonyl and Other Functional Groups." In Advanced Organic Chemistry, 219–81. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-9797-7_5.
Повний текст джерелаТези доповідей конференцій з теми "Organic groups"
Natansohn, A., P. Rochon, J. Mao, and S. Xie. "Optical Storage in Polymers Containing Azo Groups without Electron-Donor - Electron Acceptor Substituents: Poly[4-(2-methacryloyloxy)ethyl-azobenzene]." In Organic Thin Films for Photonic Applications. Washington, D.C.: Optica Publishing Group, 1993. http://dx.doi.org/10.1364/otfa.1993.wd.25.
Повний текст джерелаPadmaperuma, Asanga B., and Carlos A. Fernandez. "Heteroleptic cyclometalated Ir(III) complexes with charge transporting groups: a theoretical study." In SPIE Organic Photonics + Electronics, edited by Franky So and Chihaya Adachi. SPIE, 2012. http://dx.doi.org/10.1117/12.949510.
Повний текст джерелаBerkovic, Garry, G. M. Meshulam, Z. Kotler, A. Ben-Asuly, L. Shapiro, and V. Khodorkovsky. "Unique two-dimensional effects in the first hyper- polarizability of molecules with carbazole donor groups." In Organic Thin Films. Washington, D.C.: OSA, 1999. http://dx.doi.org/10.1364/otf.1999.sae8.
Повний текст джерелаKristanti, Novita Erma, Nafis Khuriyati, Agustinus Winarno, and Sintia Putri Pradita. "Development of Marketing Channels and Packaging Innovation on “JOSS” Organic Rice to Increase Added Value." In 3rd International Conference on Community Engagement and Education for Sustainable Development. AIJR Publisher, 2023. http://dx.doi.org/10.21467/proceedings.151.36.
Повний текст джерелаA., Cidlina, Novakova V., and Zimcik P. "Synthesis of non-peripherally substituted phthalocyanines with alkylsulfanyl groups." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013998435.
Повний текст джерелаBrown, D., A. Natansohn, P. Rochon, and S. Xie. "Optically Induced Birefringence in Copolymers and Blends Containing Azobenzene Groups." In Organic Thin Films for Photonic Applications. Washington, D.C.: Optica Publishing Group, 1993. http://dx.doi.org/10.1364/otfa.1993.thd.3.
Повний текст джерелаFort, Alain, Jacques Muller, Joel Azoulay, Marguerite Barzoukas, Valérie Alain, and Mireille Blanchard-Desce. "Characterization of Push-Pull Polyenes of Increasing Size: Linear and Quadratic Polarizabilities in Solution." In Organic Thin Films for Photonic Applications. Washington, D.C.: Optica Publishing Group, 1997. http://dx.doi.org/10.1364/otfa.1997.wc.4.
Повний текст джерелаZucolotto Cocca, Leandro Henrique, João Victor Pereira Valverde, Rafael Queiros Marcia, Alfredo Leithold Neto, Andreia Gerniski Macedo, Paula Cristina Rodrigues, Cleber Renato Mendonça, and Leonardo De Boni. "Diketopyrrolopyrrole derivatives: influence of peripheral groups in the excited states absorption process." In Organic Photonic Materials and Devices XXVI, edited by Ileana Rau, Okihiro Sugihara, and William M. Shensky. SPIE, 2024. http://dx.doi.org/10.1117/12.3002662.
Повний текст джерелаShimizu, Y., K. Oikawa, H. Monobe, K. Nakayama, B. Heinrich, and D. Guillon. "Organic Transistor with Mesophase Semiconductors Possessing Two Thienyl Groups." In 2008 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2008. http://dx.doi.org/10.7567/ssdm.2008.i-8-2.
Повний текст джерелаOstroverkhova, Oksana, Nicole Quist, Mark Li, Michael M. Haley, Ryan Tollefsen, and John Anthony. "Effect of molecular side groups and local nanoenvironment on photodegradation and its reversibility." In Organic Photonic Materials and Devices XX, edited by Christopher E. Tabor, François Kajzar, Toshikuni Kaino, and Yasuhiro Koike. SPIE, 2018. http://dx.doi.org/10.1117/12.2291065.
Повний текст джерелаЗвіти організацій з теми "Organic groups"
Knauss, K. G., and R. D. Aines. Experimental and theoretical modeling expertise of the Organic and Inorganic Environmental Geochemistry Groups. Office of Scientific and Technical Information (OSTI), December 1993. http://dx.doi.org/10.2172/218213.
Повний текст джерелаKerakova, Maria, and Emilia Varadinova. Influence of the River Bottom Substrate and Sediment Organic Component on the Macrozoobenthos Functional Feeding Groups. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, January 2020. http://dx.doi.org/10.7546/crabs.2020.01.08.
Повний текст джерелаDUDKINA, T. A. INCORPORATION OF ORGANIC MATTER INTO THE SOIL IN CROP ROTATIONS WITH DIFFERENT RATIOS OF CROP GROUPS. Ljournal, 2019. http://dx.doi.org/10.18411/issn1997-0749.2019-08-38-41.
Повний текст джерелаSantschi, Peter H. Complexation Reactions Between Trace Metals and Specific Functional Groups in Natural Organic Matter from Estuarine Waters. Fort Belvoir, VA: Defense Technical Information Center, September 2001. http://dx.doi.org/10.21236/ada626695.
Повний текст джерелаSaveleva, Viktoria. The use of a phosphor in light sources in a photo cabinet. Light sources with a phosphor in a photo cabinet using laser diodes. Intellectual Archive, July 2023. http://dx.doi.org/10.32370/iaj.2903.
Повний текст джерелаClearfield, Abraham. Organic Derivatives of Layered Group (4) Phosphates. Fort Belvoir, VA: Defense Technical Information Center, August 1988. http://dx.doi.org/10.21236/ada201080.
Повний текст джерелаYates, Jr, and John T. Organic Functional Group Reactivities at Metal Surfaces. Fort Belvoir, VA: Defense Technical Information Center, December 1988. http://dx.doi.org/10.21236/ada203094.
Повний текст джерелаHoffman, F. Retardation of volatile organic compounds in ground water in low organic carbon sediments. Office of Scientific and Technical Information (OSTI), April 1995. http://dx.doi.org/10.2172/39598.
Повний текст джерелаCastellano, Mike J., Abraham G. Shaviv, Raphael Linker, and Matt Liebman. Improving nitrogen availability indicators by emphasizing correlations between gross nitrogen mineralization and the quality and quantity of labile soil organic matter fractions. United States Department of Agriculture, January 2012. http://dx.doi.org/10.32747/2012.7597926.bard.
Повний текст джерелаBair, Kimberly. Volatile organic compound (VOC) retardation in ground water. Office of Scientific and Technical Information (OSTI), May 1996. http://dx.doi.org/10.2172/576739.
Повний текст джерела