Relevant bibliographies by topics / Organic compounds – Synthesis ; Catalysis

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Organic compounds – Synthesis ; Catalysis'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 February 2022

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Journal articles on the topic "Organic compounds – Synthesis ; Catalysis"

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Murahashi, Shun-Ichi, Hikaru Takaya, and Takeshi Naota. "Ruthenium catalysis in organic synthesis." Pure and Applied Chemistry 74, no. 1 (2002): 19–24. http://dx.doi.org/10.1351/pac200274010019.

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Ruthenium, rhodium, iridium, and rhenium hydride complexes are highly useful redox Lewis acid and base catalysts. Various substrates bearing hetero atoms are activated by these catalysts and undergo reactions with either nucleophiles or electrophiles under neutral conditions. These types of catalytic reactions are described together with their application to the preparation of various biologically active compounds.
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Baráth, Eszter. "Selective Reduction of Carbonyl Compounds via (Asymmetric) Transfer Hydrogenation on Heterogeneous Catalysts." Synthesis 52, no. 04 (2020): 504–20. http://dx.doi.org/10.1055/s-0039-1691542.

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Based on the ever-increasing demand for optically pure compounds, the development of efficient methods to produce such products is very important. Homogeneous asymmetric catalysis occupies a prominent position in the ranking of chemical transformations, with transition metals coordinated to chiral ligands being applied extensively for this purpose. However, heterogeneous catalysts have the ability to further extend the field of asymmetric transformations, because of their beneficial properties such as high stability, ease of separation and regeneration, and the possibility to apply them in con
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Li, Dongli, Panpan Wu, Ning Sun, et al. "The Diversity of Heterocyclic N-oxide Molecules: Highlights on their Potential in Organic Synthesis, Catalysis and Drug Applications." Current Organic Chemistry 23, no. 5 (2019): 616–27. http://dx.doi.org/10.2174/1385272823666190408095257.

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The synthesis and chemistry of heterocyclic N-oxide derivatives such as those from pyridine and indazole are very well-known due to their usefulness as versatile synthetic intermediates and their biological importance. These classes of organic compounds have been demonstrated in many interesting and amazing functionalities, particularly vital in the areas including metal complexes formation, catalysts design, asymmetric catalysis and synthesis, and medicinal applications (some potent N-oxide compounds with anticancer, antibacterial, anti-inflammatory activity, etc.). Therefore, the heterocycli
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Li, Junlong, Ruocan Zhuang, and Yinan Qian. "Synthesis of Novel Chalcone Derivatives by Organic Catalysis." Materials Physics and Chemistry 1, no. 1 (2018): 68. http://dx.doi.org/10.18282/mpc.v1i1.564.

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Chalcone compounds have a wide range of biological activities. In this paper, nine kinds of novel chalcone compounds were synthesized by using transacrylone derivatives and anthrone as raw materials. The effects of different catalysts and solvents on the yield of the products were investigated. The optimal catalyst was DABCO. The optimum solvent was dichloromethane with the highest yield of 71.6%. On this basis, the effect of the co-catalyst on the yield was investigated. The yield was increased to 89.9%.
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Sahoo, Biswa Mohan, and Bimal Krishna Banik. "Baker’s Yeast-Based Organocatalysis: Applications in Organic Synthesis." Current Organocatalysis 6, no. 2 (2019): 158–64. http://dx.doi.org/10.2174/2213337206666181211105304.

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Background: Catalyst speeds up any chemical reaction without changing the point of the equilibrium. Catalysis process plays a key role in organic synthesis to produce new organic compounds. Similarly, organocatalysis is a type of chemical catalysis in which the rate of a reaction is accelerated by organic catalysts. Methods: Organocatalysts have gained significant utility in organic reactions due to their less of sensitivity towards moisture, readily available, economic, large chiral pool and low toxicity as compared to metal catalysts. Organocatalysts work via both formations of covalent bond
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Imrich, Biehler, Maichle-Mössmer, and Ziegler. "Carbohydrate-Based Chiral Iodoarene Catalysts: A Survey through the Development of an Improved Catalyst Design." Molecules 24, no. 21 (2019): 3883. http://dx.doi.org/10.3390/molecules24213883.

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Iodoarene catalysts can be applied in versatile reactions, for instance in the construction of complex chiral molecules via dearomatization of simple aromatic compounds. Recently, we reported the synthesis of the first carbohydrate-based chiral iodoarene catalysts and their application in asymmetric catalysis. Here we describe the synthesis of some new and improved catalysts. An account on how we got to the improved catalyst design, as well as the X-ray structure of one of the carbohydrate-based iodoarenes, is given.
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Aneeja, Thaipparambil, Sankaran Radhika, Mohan Neetha, and Gopinathan Anilkumar. "An Overview of the One-pot Synthesis of Imidazolines." Current Organic Chemistry 24, no. 20 (2020): 2341–55. http://dx.doi.org/10.2174/1385272824999201001153735.

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One-pot syntheses are a simple, efficient and easy methodology, which are widely used for the synthesis of organic compounds. Imidazoline is a valuable heterocyclic moiety used as a synthetic intermediate, chiral auxiliary, chiral catalyst and a ligand for asymmetric catalysis. Imidazole is a fundamental unit of biomolecules that can be easily prepared from imidazolines. The one-pot method is an impressive approach to synthesize organic compounds as it minimizes the reaction time, separation procedures, and ecological impact. Many significant one-pot methods such as N-bromosuccinimide mediated
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Macarie, Lavinia, Nicoleta Plesu, Smaranda Iliescu, and Gheorghe Ilia. "Synthesis of organophosphorus compounds using ionic liquids." Reviews in Chemical Engineering 34, no. 5 (2018): 727–40. http://dx.doi.org/10.1515/revce-2017-0014.

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Abstract Organophosphorus chemistry was developed in the last decade by promoting the synthesis reactions using ionic liquids either as solvent or catalyst. Ionic liquids (ILs), the so-called “green solvents”, have gained interest in the synthesis of organophosphorus compounds as alternatives to flammable and toxic organic solvents and catalysts. ILs have beneficial properties because they provide high solubility for many organic and inorganic compounds or metal complexes, have no vapor pressure, and are reusable. Also, in some cases, they can enhance the reactivity of chemical reagents. In th
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Negishi, Ei-ichi, and Tamotsu Takahashi. "Organozirconium Compounds in Organic Synthesis." Synthesis 1988, no. 01 (1988): 1–19. http://dx.doi.org/10.1055/s-1988-27453.

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Knölker, H. J. "Iron Compounds in Organic Synthesis." Synthesis 1994, no. 10 (1994): 1106. http://dx.doi.org/10.1055/s-1994-25646.

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Dissertations / Theses on the topic "Organic compounds – Synthesis ; Catalysis"

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Jones, Charlotte E. S. "Enantioselective homogeneous catalysts for the synthesis of fluorinated organic compounds." Thesis, University of St Andrews, 2011. http://hdl.handle.net/10023/2611.

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This thesis is divided into three main results chapters that reflect the path my research took. In the first results chapter, the first organocatalyst for the carbonyl-ene reaction was discovered and found to give high conversion using 1,3-bis(3,5-bis(trifluoromethyl)phenyl)thiourea. Various carbonyl and alkene precursors were examined in the ene reaction in both catalysed and uncatalysed reactions. It was found that ene reactions using fluoral and ethyl trifluoropyruvate give higher rates of reaction when compared to other carbonyl compounds. A novel enantiopure thiourea was synthesised and t
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Huh, Billy K. "Structural effects in Fischer-Tropsch synthesis over bimetallic supported catalysts." Diss., Georgia Institute of Technology, 1985. http://hdl.handle.net/1853/11832.

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Fair, Barbara E. "An investigation of omega-phase catalysis." Diss., Georgia Institute of Technology, 1985. http://hdl.handle.net/1853/30308.

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Collins, Beatrice Samora LeFanu. "New catalytic methods and strategies for chemical synthesis." Thesis, University of Cambridge, 2014. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.648556.

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Ou, Jun, and 欧军. "Asymmetric reactions induced by phase-tagged phosphoric acid organocatalysts and copper hydride-catalyzed reductions of unsaturatedthioesters." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2011. http://hub.hku.hk/bib/B47849708.

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Two syntheses of non-cross-linked polystyrene-supported TADDOL-based phosphoric acid organocatalyst have been developed. The optimal polymer-supported catalyst 2.29d exhibited comparable catalytic activity to its small molecule counterpart in asymmetric Mannich-type reactions, and the syntheses of several chiral β-amino esters were demonstrated using 2.29d as catalyst. However, when this TADDOL-based phosphoric acid was immobilized on a polystyrene cross-linked with 1,4-bis(4-vinylphenoxy)butane, ie. JandaJelTM, the catalytic activity diminished in the first recycling and reuse of the
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Hermeke, Julia. "Chiral phosphonium ion tagged and spiroindane-based organocatalysts." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2011. http://hdl.handle.net/10722/205871.

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The research on asymmetric organocatalysis has been intensifying since the beginning of 2000. The growing interest in this research area is driven by the importance of the chemical synthesis of enantiomerically pure products. While the general field of asymmetric organocatalysis has been explored intensively, the recyclability of organocatalysts has not really been considered. The attachment of phosphonium ion phase tags to chiral binaphthyl-based phosphoric acid catalyst and the use of these materials in a range of organocatalytic asymmetric Friedel-Crafts reactions of indoles have bee
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Chen, Lingyan. "CaSH (camphor sulfonyl hydrazine) and CSI (chiral sulfonimide) organocatalysis." HKBU Institutional Repository, 2010. http://repository.hkbu.edu.hk/etd_ra/1186.

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Aparece, Mark Docto. "Synthesis of Organoboron Compounds via a Palladium-Induced 1,2-Metallate Shift Mechanism:." Thesis, Boston College, 2020. http://hdl.handle.net/2345/bc-ir:108927.

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Thesis advisor: James P. Morken<br>This dissertation describes the development of various palladium-catalyzed syntheses of organoboron compounds with the 1,2-metallate shift of organoboron “ate” complexes as a common mechanistic feature. Chapter one discusses the history of the 1,2-metallate shift with a focus on reactions promoted by transition metals, followed by my work on the palladium-catalyzed, enantioselective, halide-tolerant conjunctive cross-coupling reaction to enable the use of Grignard reagents and arylbromides. Chapter two discusses the attempt to engage allylic electrophiles in
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Lo, Kar-yan. "Gold catalysis stereoselective synthesis of propargylamines and axially chiral allenes, and application on natural product modifications /." Click to view the E-thesis via HKUTO, 2009. http://sunzi.lib.hku.hk/hkuto/record/B41758122.

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Lo, Kar-yan, and 盧嘉茵. "Gold catalysis: stereoselective synthesis of propargylamines and axially chiral allenes, and application on naturalproduct modifications." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2009. http://hub.hku.hk/bib/B41758122.

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Books on the topic "Organic compounds – Synthesis ; Catalysis"

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G, Morrell Dennis, Organic Reactions Catalysis Society, and North American Catalysis Society, eds. Catalysis of organic reactions. Marcel Dekker, 2003.

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R, Sowa John, ed. Catalysis of organic reactions. Taylor & Francis, 2005.

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Conference on the Catalysis of Organic Reactions (22nd 2008 Richmond, Virginia). Catalysis of organic reactions. Edited by Prunier Michael L. Taylor & Francis, 2008.

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A, Jannakoudakis Demetrios, ed. Electrocatalysis for organic synthesis. Wiley, 1986.

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Catalysis by polyoxometalates. J. Wiley, 2002.

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1947-, Urabe Kazuo, and Onaka Makoto 1952-, eds. Zeolite, clay, and heteropoly acid in organic reactions. Kodansha, 1992.

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Dalko, Peter I. Enantioselective organocatalysis: Reactions and experimental procedures. Wiley-VCH, 2007.

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Dʹi︠a︡konov, Vladimir A. Dzhemilev reaction in organic and organometallic synthesis. Nova Science Publishers, 2009.

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Ivanskiĭ, V. I. Kataliz v organicheskoĭ khimii: Uchebnoe posobie. Izd-vo Leningradskogo universiteta, 1985.

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Ikariya, Takao. Bifunctional Molecular Catalysis. Springer-Verlag Berlin Heidelberg, 2011.

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Book chapters on the topic "Organic compounds – Synthesis ; Catalysis"

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Wu, Hsyueh-Liang, and Ping-Yu Wu. "Rhodium(I)-Catalyzed Asymmetric Addition of Organometallic Reagents to Unsaturated Compounds." In Rhodium Catalysis in Organic Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2019. http://dx.doi.org/10.1002/9783527811908.ch5.

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Liu, Yu-Feng, and Bing-Tao Guan. "CHAPTER 2. Catalytic Use of Potassium Compounds in Organic Synthesis." In Catalysis with Earth-abundant Elements. Royal Society of Chemistry, 2020. http://dx.doi.org/10.1039/9781788012775-00028.

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Hoveyda, Amir H., Hao Wu, Suttipol Radomkit, Jeannette M. Garcia, Fredrik Haeffner, and Kang-sang Lee. "Activation of B-B and B-Si Bonds and Synthesis of Organoboron and Organosilicon Compounds through Lewis Base-Catalyzed Transformations (n?→?n* )." In Lewis Base Catalysis in Organic Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527675142.ch19.

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Brunner, Henri. "Enantioselective Synthesis of Organic Compounds with Optically Active Transition Metal Catalysts and Transition Metal Compounds." In Organometallics in Organic Synthesis 2. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74269-9_15.

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Cenini, Sergio, and Fabio Ragaini. "Synthesis of Isocyanates." In Catalytic Reductive Carbonylation of Organic Nitro Compounds. Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-017-0986-6_2.

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Cenini, Sergio, and Fabio Ragaini. "Synthesis of Heterocycles." In Catalytic Reductive Carbonylation of Organic Nitro Compounds. Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-017-0986-6_5.

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Cenini, Sergio, and Fabio Ragaini. "Synthesis of Other Non-Cyclic Compounds." In Catalytic Reductive Carbonylation of Organic Nitro Compounds. Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-017-0986-6_4.

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Hoppe, Dieter. "Synthesis of Enantiomerically Pure Unnatural Compounds Via Non-Biomimetic Homoaldol Reactions." In Enzymes as Catalysts in Organic Synthesis. Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4686-6_11.

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Cenini, Sergio, and Fabio Ragaini. "Synthesis of Carbamates and Ureas." In Catalytic Reductive Carbonylation of Organic Nitro Compounds. Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-017-0986-6_3.

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Sen, Ayusman. "Catalytic Activation of Methane and Ethane by Metal Compounds." In Activation of Unreactive Bonds and Organic Synthesis. Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/3-540-68525-1_4.

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Conference papers on the topic "Organic compounds – Synthesis ; Catalysis"

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Silveira, Claudio C., Samuel R. Mendes, and Guilherme M. Martins. "Propargylation of aromatic compounds using Ce(OTf)3 as catalyst." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0302-1.

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Lucio Martinez, Fatima, Adofo Fernández-Figueiras, Francisco Reigosa, et al. "Synthesis and catalytic study in the Suzuki-Miyaura reaction of a family of palladium compounds." In The 21st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04754.

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Iashin, D. S., and O. V. Burukhina. "Obtaining organic compounds based on Fischer-Tropsch synthesis on mixed catalyst 3% CuO, 3% Fe2O3 / Al2O3." In ТЕНДЕНЦИИ РАЗВИТИЯ НАУКИ И ОБРАЗОВАНИЯ. НИЦ «Л-Журнал», 2018. http://dx.doi.org/10.18411/lj-12-2018-154.

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Marin Figueredo, Miguel Jose, Marco Piumetti, Debora Fino, Nunzio Russo, Clarissa Cocuzza, and Samir Bensaid. "Catalytic Oxidation of Soot and Volatile Organic Compounds over Cu and Fe Doped Manganese Oxides Prepared via Sol-Gel Synthesis." In 15th International Conference on Engines & Vehicles. SAE International, 2021. http://dx.doi.org/10.4271/2021-24-0088.

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Hashmi, A. Stephen K. "NEW HORIZONS OF GOLD CATALYSIS." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-speech4.

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Alvim, Haline G. O., Tatiani B. de Lima, Heibbe C. B. Oliveira, et al. "On the Biginelli Reaction under Homogeneous Catalysis." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013915111341.

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Xiao, Zehua, Chunjing Hao, Jian Qiu, Di Xu, and Kefu Liu. "Combining catalysis with pulsed plasma for volatile organic compounds abatement." In 2017 IEEE International Conference on Plasma Science (ICOPS). IEEE, 2017. http://dx.doi.org/10.1109/plasma.2017.8496263.

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Neto, B. A. D. "Catalysis and mechanistic investigation with ionically-tagged reagents." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-yong1.

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Marini, F., M. Tiecco, L. Testaferri та ін. "Catalyst-controlled Asymmetric Syntheses of Organoselenium Compounds. β-Hydroxyselenides by Desymmetrization of meso Epoxides". У The 11th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2007. http://dx.doi.org/10.3390/ecsoc-11-01343.

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Xiao, Zehua, and Kefu Liu. "Combining catalysis with non-thermal plasma for volatile organic compounds abatement." In 2015 IEEE International Conference on Plasma Sciences (ICOPS). IEEE, 2015. http://dx.doi.org/10.1109/plasma.2015.7179883.

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Reports on the topic "Organic compounds – Synthesis ; Catalysis"

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Reilly, S. D., D. R. Click, S. K. Grumbine, B. L. Scott, and J. G. Watkins. Asymmetric catalysis in organic synthesis. Office of Scientific and Technical Information (OSTI), 1998. http://dx.doi.org/10.2172/677032.

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Wiemers, K. D., H. Babad, R. T. Hallen, L. P. Jackson, and M. E. Lerchen. An Assessment of the Stability and the Potential for In-Situ Synthesis of Regulated Organic Compounds in High Level Radioactive Waste Stored at Hanford, Richland, Washington. Office of Scientific and Technical Information (OSTI), 1999. http://dx.doi.org/10.2172/2535.

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