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Artykuły w czasopismach na temat "Organic groups"
Yamamoto, Katsutoshi, Yuki Nohara, Yusuke Domon, Yoko Takahashi, Yasuyuki Sakata, Jacques Plévert i Takashi Tatsumi. "Organic−Inorganic Hybrid Zeolites with Framework Organic Groups". Chemistry of Materials 17, nr 15 (lipiec 2005): 3913–20. http://dx.doi.org/10.1021/cm048367g.
Pełny tekst źródłaWan, Ying, Dieqing Zhang, Na Hao i Dongyuan Zhao. "Organic groups functionalised mesoporous silicates". International Journal of Nanotechnology 4, nr 1/2 (2007): 66. http://dx.doi.org/10.1504/ijnt.2007.012316.
Pełny tekst źródłaHodge, P. "Protective groups in organic synthesis". Polymer 33, nr 16 (styczeń 1992): 3542. http://dx.doi.org/10.1016/0032-3861(92)91123-j.
Pełny tekst źródłaWilson, A. J. C. "Space groups rare for organic compounds". Acta Crystallographica Section A Foundations of Crystallography 43, a1 (12.08.1987): C289. http://dx.doi.org/10.1107/s0108767387077717.
Pełny tekst źródłaDral, A. Petra, i Johan E. ten Elshof. "Organic groups influencing microporosity in organosilicas". Microporous and Mesoporous Materials 267 (wrzesień 2018): 267–73. http://dx.doi.org/10.1016/j.micromeso.2018.03.036.
Pełny tekst źródłaCreyghton, Edward J. "Organic groups cling to the pores". Nature 393, nr 6680 (maj 1998): 21–22. http://dx.doi.org/10.1038/29886.
Pełny tekst źródłaRavikumar, Velayutham, Andrea Fin, Naomi Sakai i Stefan Matile. "Solubilising groups: a conceptual equivalent of protecting groups in organic synthesis". Supramolecular Chemistry 23, nr 1-2 (31.08.2010): 69–73. http://dx.doi.org/10.1080/10610278.2010.510193.
Pełny tekst źródłaSurtiningsih, Tini, Fatimah Fatimah, Ni’matuzahroh Ni’matuzahroh, Agus Supriyanto i Tri Nurhariyati. "PELATIHAN PEMBUATAN PUPUK ORGANIK CAIR PADA KELOMPOK TANI DI KABUPATEN PROBOLINGGO". Jurnal Layanan Masyarakat (Journal of Public Services) 2, nr 1 (10.06.2020): 21. http://dx.doi.org/10.20473/jlm.v2i1.2018.21-24.
Pełny tekst źródłaJarowicki, Krzysztof, i Philip Kocienski. "Protecting groups". Contemporary Organic Synthesis 2, nr 5 (1995): 315. http://dx.doi.org/10.1039/co9950200315.
Pełny tekst źródłaJarowicki, Krzysztof, i Philip Kocienski. "Protecting groups". Contemporary Organic Synthesis 3, nr 5 (1996): 397. http://dx.doi.org/10.1039/co9960300397.
Pełny tekst źródłaRozprawy doktorskie na temat "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.
Pełny tekst źródłaMouselmani, Rim. "Reduction of Organic Functional Groups Using Hypophosphites". Thesis, Lyon, 2018. http://www.theses.fr/2018LYSE1241/document.
Pełny tekst źródłaRecently, 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.
Pełny tekst źródłaLee, 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.
Pełny tekst źródłaAhmed, 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.
Pełny tekst źródłaHussain, 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.
Pełny tekst źródłaLongstaff, Peter A. "Novel side chain protecting groups for solid phase peptide synthesis". Thesis, University of Edinburgh, 1989. http://hdl.handle.net/1842/15232.
Pełny tekst źródłaKorzycka, 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.
Pełny tekst źródłaHe, 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.
Pełny tekst źródłaDeodhar, 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.
Pełny tekst źródłaKsiążki na temat "Organic groups"
Protecting groups. Wyd. 3. Stuttgart: Georg Thieme, 2004.
Znajdź pełny tekst źródłaProtecting groups. Stuttgart: G. Thieme, 2000.
Znajdź pełny tekst źródłaProtecting groups. Stuttgart: G. Thieme, 1994.
Znajdź pełny tekst źródłaM, Wuts Peter G., red. Protective groups in organic synthesis. Wyd. 3. New York: Wiley, 1999.
Znajdź pełny tekst źródłaMcOmie, J. F. W., red. Protective Groups in Organic Chemistry. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4684-7218-9.
Pełny tekst źródłaGreene, Theodora W. Protective groups in organic synthesis. Wyd. 2. New York: Wiley, 1991.
Znajdź pełny tekst źródłaWuts, Peter G. M., red. Greene's Protective Groups in Organic Synthesis. Hoboken, New Jersey: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118905074.
Pełny tekst źródłaGordon, Hanna J., red. Quantitative organic analysis via functional groups. Wyd. 4. Malabar, Fla: R.E. Krieger Pub. Co., 1988.
Znajdź pełny tekst źródłaR, Katritzky Alan, Meth-Cohn Otto, Rees Charles W i Ley Steven V, red. Comprehensive organic functional group transformations. Oxford: Pergamon, 1995.
Znajdź pełny tekst źródłaR, Katritzky Alan, Meth-Cohn Otto, Rees Charles W i Pattenden Gerald, red. Comprehensive organic functional group transformations. Oxford: Pergamon, 1995.
Znajdź pełny tekst źródłaCzęści książek na temat "Organic groups"
Sarker, Satyajit D., i Lutfun Nahar. "Organic Functional Groups". W Chemistry for Pharmacy Students, 59–189. West Sussex, England: John Wiley & Sons, Ltd,., 2013. http://dx.doi.org/10.1002/9781118687529.ch4.
Pełny tekst źródłaBoons, G. J. "Protecting Groups". W Organic Synthesis with Carbohydrates, 26–55. Sheffield, UK: Sheffield Academic Press Ltd, 2008. http://dx.doi.org/10.1002/9780470760321.ch2.
Pełny tekst źródłaGutman, Ivan, i Oskar E. Polansky. "Automorphism Groups". W 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.
Pełny tekst źródłaGutman, Ivan, i Oskar E. Polansky. "Symmetry Groups". W 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.
Pełny tekst źródłaBurgess, D. A. "Organic Chemistry — Functional Groups". W Work Out Chemistry ‘A’ Level, 158–68. London: Macmillan Education UK, 1987. http://dx.doi.org/10.1007/978-1-349-24067-8_12.
Pełny tekst źródłaVančik, Hrvoj. "Functional Groups". W 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.
Pełny tekst źródłaVančik, Hrvoj. "Functional Groups". W 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.
Pełny tekst źródłaSaunders, K. J. "Other Aromatic Polymers Containing p-Phenylene Groups". W Organic Polymer Chemistry, 265–85. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-009-1195-6_12.
Pełny tekst źródłaCarey, Francis A., i Richard J. Sundberg. "Reactions of Carbon Nucleophiles with Carbonyl Groups". W Advanced Organic Chemistry, 55–120. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-9797-7_2.
Pełny tekst źródłaCarey, Francis A., i Richard J. Sundberg. "Reduction of Carbonyl and Other Functional Groups". W Advanced Organic Chemistry, 219–81. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4613-9797-7_5.
Pełny tekst źródłaStreszczenia konferencji na temat "Organic groups"
Natansohn, A., P. Rochon, J. Mao i S. Xie. "Optical Storage in Polymers Containing Azo Groups without Electron-Donor - Electron Acceptor Substituents: Poly[4-(2-methacryloyloxy)ethyl-azobenzene]". W Organic Thin Films for Photonic Applications. Washington, D.C.: Optica Publishing Group, 1993. http://dx.doi.org/10.1364/otfa.1993.wd.25.
Pełny tekst źródłaPadmaperuma, Asanga B., i Carlos A. Fernandez. "Heteroleptic cyclometalated Ir(III) complexes with charge transporting groups: a theoretical study". W SPIE Organic Photonics + Electronics, redaktorzy Franky So i Chihaya Adachi. SPIE, 2012. http://dx.doi.org/10.1117/12.949510.
Pełny tekst źródłaBerkovic, Garry, G. M. Meshulam, Z. Kotler, A. Ben-Asuly, L. Shapiro i V. Khodorkovsky. "Unique two-dimensional effects in the first hyper- polarizability of molecules with carbazole donor groups". W Organic Thin Films. Washington, D.C.: OSA, 1999. http://dx.doi.org/10.1364/otf.1999.sae8.
Pełny tekst źródłaKristanti, Novita Erma, Nafis Khuriyati, Agustinus Winarno i Sintia Putri Pradita. "Development of Marketing Channels and Packaging Innovation on “JOSS” Organic Rice to Increase Added Value". W 3rd International Conference on Community Engagement and Education for Sustainable Development. AIJR Publisher, 2023. http://dx.doi.org/10.21467/proceedings.151.36.
Pełny tekst źródłaA., Cidlina, Novakova V. i Zimcik P. "Synthesis of non-peripherally substituted phthalocyanines with alkylsulfanyl groups". W 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013998435.
Pełny tekst źródłaBrown, D., A. Natansohn, P. Rochon i S. Xie. "Optically Induced Birefringence in Copolymers and Blends Containing Azobenzene Groups". W Organic Thin Films for Photonic Applications. Washington, D.C.: Optica Publishing Group, 1993. http://dx.doi.org/10.1364/otfa.1993.thd.3.
Pełny tekst źródłaFort, Alain, Jacques Muller, Joel Azoulay, Marguerite Barzoukas, Valérie Alain i Mireille Blanchard-Desce. "Characterization of Push-Pull Polyenes of Increasing Size: Linear and Quadratic Polarizabilities in Solution". W Organic Thin Films for Photonic Applications. Washington, D.C.: Optica Publishing Group, 1997. http://dx.doi.org/10.1364/otfa.1997.wc.4.
Pełny tekst źródłaZucolotto Cocca, Leandro Henrique, João Victor Pereira Valverde, Rafael Queiros Marcia, Alfredo Leithold Neto, Andreia Gerniski Macedo, Paula Cristina Rodrigues, Cleber Renato Mendonça i Leonardo De Boni. "Diketopyrrolopyrrole derivatives: influence of peripheral groups in the excited states absorption process". W Organic Photonic Materials and Devices XXVI, redaktorzy Ileana Rau, Okihiro Sugihara i William M. Shensky. SPIE, 2024. http://dx.doi.org/10.1117/12.3002662.
Pełny tekst źródłaShimizu, Y., K. Oikawa, H. Monobe, K. Nakayama, B. Heinrich i D. Guillon. "Organic Transistor with Mesophase Semiconductors Possessing Two Thienyl Groups". W 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.
Pełny tekst źródłaOstroverkhova, Oksana, Nicole Quist, Mark Li, Michael M. Haley, Ryan Tollefsen i John Anthony. "Effect of molecular side groups and local nanoenvironment on photodegradation and its reversibility". W Organic Photonic Materials and Devices XX, redaktorzy Christopher E. Tabor, François Kajzar, Toshikuni Kaino i Yasuhiro Koike. SPIE, 2018. http://dx.doi.org/10.1117/12.2291065.
Pełny tekst źródłaRaporty organizacyjne na temat "Organic groups"
Knauss, K. G., i R. D. Aines. Experimental and theoretical modeling expertise of the Organic and Inorganic Environmental Geochemistry Groups. Office of Scientific and Technical Information (OSTI), grudzień 1993. http://dx.doi.org/10.2172/218213.
Pełny tekst źródłaKerakova, Maria, i 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, styczeń 2020. http://dx.doi.org/10.7546/crabs.2020.01.08.
Pełny tekst źródłaDUDKINA, 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.
Pełny tekst źródłaSantschi, 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, wrzesień 2001. http://dx.doi.org/10.21236/ada626695.
Pełny tekst źródłaSaveleva, 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, lipiec 2023. http://dx.doi.org/10.32370/iaj.2903.
Pełny tekst źródłaClearfield, Abraham. Organic Derivatives of Layered Group (4) Phosphates. Fort Belvoir, VA: Defense Technical Information Center, sierpień 1988. http://dx.doi.org/10.21236/ada201080.
Pełny tekst źródłaYates, Jr, i John T. Organic Functional Group Reactivities at Metal Surfaces. Fort Belvoir, VA: Defense Technical Information Center, grudzień 1988. http://dx.doi.org/10.21236/ada203094.
Pełny tekst źródłaHoffman, F. Retardation of volatile organic compounds in ground water in low organic carbon sediments. Office of Scientific and Technical Information (OSTI), kwiecień 1995. http://dx.doi.org/10.2172/39598.
Pełny tekst źródłaCastellano, Mike J., Abraham G. Shaviv, Raphael Linker i 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, styczeń 2012. http://dx.doi.org/10.32747/2012.7597926.bard.
Pełny tekst źródłaBair, Kimberly. Volatile organic compound (VOC) retardation in ground water. Office of Scientific and Technical Information (OSTI), maj 1996. http://dx.doi.org/10.2172/576739.
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