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Artykuły w czasopismach na temat "Organic reaction methodology"
Chinchilla, Rafael, i Carmen Nájera. "The Sonogashira Reaction: A Booming Methodology in Synthetic Organic Chemistry†". Chemical Reviews 107, nr 3 (marzec 2007): 874–922. http://dx.doi.org/10.1021/cr050992x.
Pełny tekst źródłaSharma, Sulekha. "Electro-organic Reactions: Direct and Indirect Electrolysis". Oriental Journal Of Chemistry 40, nr 2 (30.04.2024): 321–32. http://dx.doi.org/10.13005/ojc/400202.
Pełny tekst źródłaNoor, Rida, Ameer Fawad Zahoor, Muhammad Irfan, Syed Makhdoom Hussain, Sajjad Ahmad, Ali Irfan, Katarzyna Kotwica-Mojzych i Mariusz Mojzych. "Transition Metal Catalyzed Hiyama Cross-Coupling: Recent Methodology Developments and Synthetic Applications". Molecules 27, nr 17 (2.09.2022): 5654. http://dx.doi.org/10.3390/molecules27175654.
Pełny tekst źródłaLei, Ming, Qingtong Zhang, Douyong Min i Shuangfei Wang. "The Treatment of Absorbable Organic Halogens and Organic Compounds in Simulated Bleaching Effluents Through the Response Surface Methodology Optimized Fenton System". Journal of Biobased Materials and Bioenergy 14, nr 2 (1.04.2020): 280–86. http://dx.doi.org/10.1166/jbmb.2020.1949.
Pełny tekst źródłaJimenez, David Esteban Quintero, Lucas Lima Zanin, Luan Farinelli Diniz, Javier Ellena i André Luiz Meleiro Porto. "Green Synthetic Methodology of (E)-2-cyano-3-aryl Selective Knoevenagel Adducts Under Microwave Irradiation". Current Microwave Chemistry 6, nr 1 (24.10.2019): 54–60. http://dx.doi.org/10.2174/2213335606666190906123431.
Pełny tekst źródłaLei, Jie, Jia Xu, Dian-Yong Tang, Jing-Wei Shao, Hong-yu Li, Zhong-Zhu Chen i Zhi-Gang Xu. "A concise and unexpected one-pot methodology for the synthesis of pyrazinone-fused pyridones". Organic Chemistry Frontiers 7, nr 18 (2020): 2657–63. http://dx.doi.org/10.1039/d0qo00590h.
Pełny tekst źródłaHakkou, H., D. Carrié, L. Paquin i J. P. Bazureau. "Ionic liquid-phase organic synthesis (IoLiPOS) methodology applied to cross aldol reaction". Russian Journal of Organic Chemistry 47, nr 3 (marzec 2011): 371–73. http://dx.doi.org/10.1134/s1070428011030079.
Pełny tekst źródłaReddy, K. Sateesh, Bandi Siva, S. Divya Reddy, N. Reddy Naresh, T. V. Pratap, B. Venkateswara Rao, Yi-An Hong i in. "In Situ FTIR Spectroscopic Monitoring of the Formation of the Arene Diazonium Salts and Its Applications to the Heck–Matsuda Reaction". Molecules 25, nr 9 (8.05.2020): 2199. http://dx.doi.org/10.3390/molecules25092199.
Pełny tekst źródłaRadhika, Sankaran, Mohan Neetha, Thaipparambil Aneeja i Gopinathan Anilkumar. "Microwave-assisted Amination Reactions: An Overview". Current Organic Chemistry 24, nr 19 (1.12.2020): 2235–55. http://dx.doi.org/10.2174/1385272824999200914111246.
Pełny tekst źródłaRoy, Snigdha. "Prins-Friedel-Crafts Cyclization: Synthesis of Diversely Functionalized Six- Membered Oxacycles". Current Organic Chemistry 25, nr 5 (15.03.2021): 635–51. http://dx.doi.org/10.2174/1385272825666210114105020.
Pełny tekst źródłaRozprawy doktorskie na temat "Organic reaction methodology"
Bhuiyan, Mosharef Hossain. "Synthetic organic reaction new methodology and applications". Thesis, University of North Bengal, 2003. http://hdl.handle.net/123456789/772.
Pełny tekst źródłaBiswas, Kinkar. "Development of organic reaction methodology using polymar-supported reagents, focused microwaves and on-water chemistry". Thesis, University of North Bengal, 2016. http://ir.nbu.ac.in/handle/123456789/2745.
Pełny tekst źródłaLarson, Shawn E. "Enantioselective Brønsted and Lewis Acid-Catalyzed Reaction Methodology: Aziridines as Building Blocks for Catalytic Asymmetric Induction". Scholar Commons, 2012. http://scholarcommons.usf.edu/etd/4357.
Pełny tekst źródłaCavitt, Marchello Alfonzo. "Stress relief: Exercising Lewis acid catalysis for donor-acceptor cyclopropane ring-opening annulations, a basis for new reaction methodologies". Diss., Georgia Institute of Technology, 2015. http://hdl.handle.net/1853/54448.
Pełny tekst źródłaPelletier, Sophie Marie-Clémentine. "One-pot nitro-Mannich cascade reactions : new methodologies and synthetic applications". Thesis, University of Oxford, 2011. http://ora.ox.ac.uk/objects/uuid:283641bf-bb4e-48a8-8a28-2e048b8c4ea6.
Pełny tekst źródłaMartinez, Ariza Guillermo, i Ariza Guillermo Martinez. "Exploiting Molecular Diversity to Access Biologically Relevant Chemotypes". Diss., The University of Arizona, 2016. http://hdl.handle.net/10150/621718.
Pełny tekst źródłaJha, Satadru. "Organic reactions methodology : studies on carbon-nitrogen hetero bond forming reactions". Thesis, University of North Bengal, 2004. http://hdl.handle.net/123456789/745.
Pełny tekst źródłaBaldwin, I. Craig. "New methodology involving allylic substitution and conjugate addition reactions". Thesis, Loughborough University, 1996. https://dspace.lboro.ac.uk/2134/27583.
Pełny tekst źródłaDas, Pralay. "New reactions and methodology : studies on transition metal catalyzed organic transformations". Thesis, University of North Bengal, 2005. http://hdl.handle.net/123456789/775.
Pełny tekst źródłaBentley, Scott Alexander. "Asymmetric conjugate addition reactions". Thesis, University of Oxford, 2011. http://ora.ox.ac.uk/objects/uuid:9e619a66-6277-48c2-8a2e-24f8206e52b3.
Pełny tekst źródłaKsiążki na temat "Organic reaction methodology"
Sun, Xiaoping. Organic mechanisms: Reactions, methodology, and biological applications. Hoboken, New Jersey: Wiley, 2013.
Znajdź pełny tekst źródłaBoger, Dale L. Hetero Diels-Alder methodology in organic synthesis. San Diego: Academic Press, 1987.
Znajdź pełny tekst źródłaBoger, Dale L. Hetero Diels-Alder methodology inorganic synthesis. San Diego: Academic Press, 1987.
Znajdź pełny tekst źródłaInternational Symposium on Organic Reactions (1991 Kyoto, Japan). Modern methodology in organic synthesis: Proceedings of the 1991 International Symposium on Organic Reactions, Kyoto. Tokyo: Kodansha, 1992.
Znajdź pełny tekst źródłaSun, Xiaoping. Organic Mechanisms: Reactions, Methodology, and Biological Applications. Wiley & Sons, Incorporated, John, 2013.
Znajdź pełny tekst źródłaSun, Xiaoping. Organic Mechanisms: Reactions, Methodology, and Biological Applications. Wiley & Sons, Limited, John, 2021.
Znajdź pełny tekst źródłaSun, Xiaoping. Organic Mechanisms: Reactions, Methodology, and Biological Applications. Wiley & Sons, Incorporated, John, 2020.
Znajdź pełny tekst źródłaSun, Xiaoping. Organic Mechanisms: Reactions, Methodology, and Biological Applications. Wiley & Sons, Incorporated, John, 2013.
Znajdź pełny tekst źródłaSun, Xiaoping. Organic Mechanisms: Reactions, Methodology, and Biological Applications. Wiley & Sons, Incorporated, John, 2020.
Znajdź pełny tekst źródłaSun, Xiaoping. Organic Mechanisms: Reactions, Methodology, and Biological Applications. Wiley & Sons, Incorporated, John, 2013.
Znajdź pełny tekst źródłaCzęści książek na temat "Organic reaction methodology"
Hirano, Takashi, i Chihiro Matsuhashi. "Soft Crystal Chemiluminescence Systems Using Organic Peroxides". W The Materials Research Society Series, 155–77. Singapore: Springer Nature Singapore, 2023. http://dx.doi.org/10.1007/978-981-99-0260-6_9.
Pełny tekst źródłaGhosh, Mithun Kumar, i Tanmay Kumar Ghorai. "Advantages of Nanocatalysts on Knoevenagel Condensation". W Diverse Strategies for Catalytic Reactions, 119–39. BENTHAM SCIENCE PUBLISHERS, 2023. http://dx.doi.org/10.2174/9789815079036123020007.
Pełny tekst źródłaNakamura, Eiichi. "Me3SiCl-accelerated conjugate addition reactions of organocopper reagents". W Organocopper Reagents: A Practical Approach, 129–42. Oxford University PressOxford, 1995. http://dx.doi.org/10.1093/oso/9780198557579.003.0006.
Pełny tekst źródłaSu, Z., i L. A. Paquette,. "Synthesis of an Enantiopure C-4 Functionalised 2-Iodocyclohexanone Acetal". W Exercises in Synthetic Organic Chemistry, 29. Oxford University PressOxford, 1997. http://dx.doi.org/10.1093/oso/9780198559443.003.0022.
Pełny tekst źródłaGovind, Rakesh, Shiva Charan i Jack Baltzersen. "Systematic Generation of Reactions Pathways for Manufacturing Bulk Industrial Chemicals from Biomass". W Biomass [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.103123.
Pełny tekst źródłaLi, Jie Jack, Chris Limberakis i Derek A. Pflum. "Carbon−Carbon Bond Formation". W Modern Organic Synthesis in the Laboratory. Oxford University Press, 2008. http://dx.doi.org/10.1093/oso/9780195187984.003.0011.
Pełny tekst źródłaBhatia, B., T. Punniyamurthy i J. Iqbal. "Oxidation of the C—H bond". W Asymmetric Oxidation Reactions, 5–18. Oxford University PressOxford, 2001. http://dx.doi.org/10.1093/oso/9780198502012.003.0002.
Pełny tekst źródłaDaly, Francis P., William M. Jensen i Daniel J. Ostgard. "Influence of Catalyst Preparation Methodology on the Selectivity of Supported Transition Metal Catalysts". W Catalysis of Organic Reactions, 13–21. Routledge, 2017. http://dx.doi.org/10.1201/9781315138855-2.
Pełny tekst źródłaChemla, F., i A. Pérez-Luna. "2.5 Radical–Polar Crossover Reactions". W Free Radicals: Fundamentals and Applications in Organic Synthesis 2. Stuttgart: Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/sos-sd-233-00075.
Pełny tekst źródłaReiss-Husson, F., i D. Picot. "Crystallization of Membrane Proteins". W Crystallization of Nucleic Acids and Proteins. Oxford University Press, 1999. http://dx.doi.org/10.1093/oso/9780199636792.003.0013.
Pełny tekst źródłaStreszczenia konferencji na temat "Organic reaction methodology"
Mereu, Federico, Jayangi D. Wagaarachchige, Zulkifli Idris, Klaus-Joachim Jens i Maths Halstensen. "Response Surface Modelling to Reduce CO2 Capture Solvent Cost by Conversion of OZD to MEA". W 64th International Conference of Scandinavian Simulation Society, SIMS 2023 Västerås, Sweden, September 25-28, 2023. Linköping University Electronic Press, 2023. http://dx.doi.org/10.3384/ecp200003.
Pełny tekst źródłaBurge, Scott R. "Automated Analysis of Trichloroethene and Chloroform". W ASME 2003 9th International Conference on Radioactive Waste Management and Environmental Remediation. ASMEDC, 2003. http://dx.doi.org/10.1115/icem2003-4648.
Pełny tekst źródłaTioni, Estevan, i Pascal Rousseaux. "BRINGING TOGETHER MICROWAVE ASSISTED SYNTHESIS AND CHEMICAL ENGINEERING PRINCIPLES". W Ampere 2019. Valencia: Universitat Politècnica de València, 2019. http://dx.doi.org/10.4995/ampere2019.2019.9901.
Pełny tekst źródłaZheng, Zhenguo, Oscar Julian Jaramillo, Jhon Patiño, John Fredy Reina i Carlos Francisco Pacheco. "Successful Acid Stimulation in Limestone - Tobo-Monserrate Formation in Gigante Field - Colombia". W SPE Annual Technical Conference and Exhibition. SPE, 2021. http://dx.doi.org/10.2118/206037-ms.
Pełny tekst źródłaFerreira, Jorge A., João E. de Oliveira i Vitor A. Costa. "Modeling of Hydraulic Systems for Hardware-in-the-Loop Simulation: A Methodology Proposal". W ASME 1999 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 1999. http://dx.doi.org/10.1115/imece1999-0766.
Pełny tekst źródłaTsai, Lung-Wen, Dar-Zen Chen i Ta-Wei Lin. "Dynamic Analysis of Geared Robotic Mechanisms Using Graph Theory". W ASME 1996 Design Engineering Technical Conferences and Computers in Engineering Conference. American Society of Mechanical Engineers, 1996. http://dx.doi.org/10.1115/96-detc/mech-1554.
Pełny tekst źródłaJiang, Li, Suzanne Stewart i Jonathan Abbott. "Downhole Mineral Scale Dissolution Booster". W Offshore Technology Conference. OTC, 2022. http://dx.doi.org/10.4043/32069-ms.
Pełny tekst źródłaJiang, Li, Suzanne Stewart i Jonathan Abbott. "Downhole Mineral Scale Dissolution Booster". W Offshore Technology Conference. OTC, 2022. http://dx.doi.org/10.4043/32069-ms.
Pełny tekst źródłaMoreira da Silva, Fernando. "Color processing and human perception". W Intelligent Human Systems Integration (IHSI 2023) Integrating People and Intelligent Systems. AHFE International, 2023. http://dx.doi.org/10.54941/ahfe1002840.
Pełny tekst źródłaRaporty organizacyjne na temat "Organic reaction methodology"
Hochman, Ayala, Thomas Nash III i Pamela Padgett. Physiological and Biochemical Characterization of the Effects of Oxidant Air Pollutants, Ozone and Gas-phase Nitric Acid, on Plants and Lichens for their Use as Early Warning Biomonitors of these Air Pollutants. United States Department of Agriculture, styczeń 2011. http://dx.doi.org/10.32747/2011.7697115.bard.
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