Academic literature on the topic 'Organic reaction'

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Journal articles on the topic "Organic reaction"

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Christoffers, Jens, and David Kieslich. "Cyanide Anions as Nucleophilic Catalysts in Organic Synthesis." Synthesis 53, no. 19 (2021): 3485–96. http://dx.doi.org/10.1055/a-1499-8943.

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AbstractThe nucleophilic addition of a cyanide anion to a carbonyl group is the basis for several cyanide-catalyzed organic reactions, which are summarized in this review. Since cyanide is also a good leaving group, it is an excellent catalyst for transacylation reactions. As an electron-withdrawing group, it also stabilizes a negative charge in its α-position, thus allowing the umpolung of aldehydes to formyl anion equivalents. The two leading examples are the benzoin condensation and the Michael–Stetter reaction furnishing α-hydroxy ketones and 1,4-dicarbonyl compounds, which are both cataly
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THIBBLIN, A. "ChemInform Abstract: Elimination Reactions (Organic Reaction Mechanisms)." ChemInform 22, no. 45 (2010): no. http://dx.doi.org/10.1002/chin.199145330.

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Herges, Rainer. "Reaction planning: prediction of new organic reactions." Journal of Chemical Information and Modeling 30, no. 4 (1990): 377–83. http://dx.doi.org/10.1021/ci00068a006.

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BOWMAN, W. R. "ChemInform Abstract: Radical Reactions (Organic Reaction Mechanisms)." ChemInform 25, no. 13 (2010): no. http://dx.doi.org/10.1002/chin.199413284.

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RHODES, C. J. "ChemInform Abstract: Radical Reactions (Organic Reaction Mechanisms)." ChemInform 25, no. 13 (2010): no. http://dx.doi.org/10.1002/chin.199413285.

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Jain, S. C., S. Talwar, Sunita Bhagat, V. K. Raiwanshi, R. Kumar, and B. Ravindra Babu. "Novel reaction products from simple organic reactions: Delineation of reaction pathways." Pure and Applied Chemistry 68, no. 3 (1996): 739–42. http://dx.doi.org/10.1351/pac199668030739.

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Mendenhall, G. David. "An organic "reaction"." Journal of Chemical Education 67, no. 6 (1990): 538. http://dx.doi.org/10.1021/ed067p538.

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Hanson, J. R. "Organic reaction mechanisms." Journal of Organometallic Chemistry 689, no. 18 (2004): 2946. http://dx.doi.org/10.1016/j.jorganchem.2004.04.018.

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Schreiner, Peter R. "Organic Reaction Mechanisms." European Journal of Organic Chemistry 2019, no. 2-3 (2019): 232. http://dx.doi.org/10.1002/ejoc.201801860.

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Diminguez, B. "Organic Reaction Mechanisms." Synthesis 2002, no. 12 (2002): 1780. http://dx.doi.org/10.1055/s-2002-33640.

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Dissertations / Theses on the topic "Organic reaction"

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Roscini, Claudio. "Reaction Control in Organic Photochemistry." Thesis, University of Bristol, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.521102.

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Edwards, M. R. "Organic reaction pathways from crystal structures." Thesis, University of Cambridge, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.355674.

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El-Kaddar, Yousef Younis. "Organosilicon reaction mechanisms." Thesis, University of Sussex, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.375169.

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This thesis is concerned with the preparation and reactions of some highly sterically hindered organosilicon compounds, mainly of the type TeiSiMe2X where Tsi denotes the (Me3Si)3C group. The first detailed study of the reactions of TsiS1Me20CN has shown that reactions with NaN3 in MeOH or KSCN or KOCN in MeCN give exclusively the corresponding TsiSiMe2X compounds (X = N3, NCS, or NCO), whereas those with other salts, viz. LiCl, CsF, KSCN, and KOCN, give the TsiSiMe2X species along· with other products, including in many cases TsiSiMe2NCO and TsiSiMe20H (from traces of water), and (in MeOH) Ts
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Jha, Jay Shankar. "[3+2] Cycloaddition Reaction of Gem-Dicyanoepoxide and Electrophilic Reaction of Ethyl Atropate." Thesis, Southern Illinois University at Edwardsville, 2013. http://pqdtopen.proquest.com/#viewpdf?dispub=1545300.

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<p> The epoxide-olefin [3+2] cycloaddition reaction is an important tool in synthesizing heterocyclic five member rings. Such cyclic compounds are well known for the formation of biologically active compounds. In this experiment, we developed a method for a [3+2] cycloaddition reaction between gem-dicyano phenyl epoxide and diethyl (E)-2-fluoromaleate to synthesize 2, 2-dicyano-3, 4-diethoxycarbonyl-4-fluoro-5-phenylfuran. The yield of the product was 55.56 %. </p><p> Fluorine is small in size and is the most electronegative element. These properties of fluorine make its incorporation into
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Tait, Joanne Margaret. "Water-promoted reactions for organic synthesis : the Claisen rearrangement and the Baylis-Hillman reaction." Thesis, University of Reading, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.250705.

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Gauvreau, Danny. "Enantioselective tandem oxy-copeene reaction." Thesis, University of Ottawa (Canada), 2003. http://hdl.handle.net/10393/26374.

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The tandem oxy-Cope/ene reaction allows the rapid construction of complex structures in a few steps. It was notably used in the total synthesis of (+)-arteannium M where the cascade revealed to be highly diastereoselective and enantioselective. The hypothesis that the retention of chirality based on the rigidity of an intermediate atropisomer devoid of stereogenic centers was proposed. This document presents a study of the enantioselectivity of the tandem oxy-Cope/ene reaction and provides an explanation for the decrease in chirality observed during the cascade. Different variables of the reac
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Ramírez, Artero Jesús. "Catalytic diboration reaction towards the organic functionalization." Doctoral thesis, Universitat Rovira i Virgili, 2007. http://hdl.handle.net/10803/9091.

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Els compostos organoborats són intermedis de reacció molt valuosos en síntesi orgànica, degut a que l'enllaç carboni-bor pot ser derivatitzat de múltiples maneres. La diboració catalitzada d'alquins i alquens ha estat ampliament estudiada en els darrers quinze anys, essent la diboració catalitzada d'alquins un procés en el que s'han obtingut elevats rendiments i activitats. No obstant això, en la diboració catalitzada d'alquens la presència de la reacció secundaria de b-eliminació de H sempre s'ha presentat com un seriós inconvenient, impedint un bon compromís entre activitat catalítica i quim
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Conner, Keyanna M. "Gas Phase Studies of Organic Reaction Mechanisms." VCU Scholars Compass, 2015. http://scholarscompass.vcu.edu/etd/4032.

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The competition between substitution (SN2) and elimination (E2) in nucleophilic reactions of alkyl halides has had a profound influence on the development of physical organic chemistry and remains an important testing ground for identifying reactivity patterns in gas-phase organic chemistry. Here, the competition between substitution and elimination, as well as the regioselectivity of E2 reactions have been examined in the gas phase. By doing so, the intrinsic reactivity patterns can be probed in the absence of solvation effects. The SN2 and E2 reactions of a large set of alkyl bromides with v
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Chung, Lung Wa. "Computational studies of the reaction mechanisms and stereochemistry of metal-mediated organic reactions /." View abstract or full-text, 2006. http://library.ust.hk/cgi/db/thesis.pl?CHEM%202006%20CHUNG.

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Sheikh, Junaid. "Rapid pressure swing reaction processes." Thesis, Imperial College London, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.311951.

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Books on the topic "Organic reaction"

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Spiers, Paul. Organic reaction mechanisms. Daniels, 1991.

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K, Parashar R., ed. Organic reaction mechanisms. CRC Press, 2002.

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Knipe, A. C., and W. E. Watts, eds. Organic Reaction Mechanisms. John Wiley & Sons, Ltd., 1987. http://dx.doi.org/10.1002/9780470319536.

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Knipe, A. C., and W. E. Watts, eds. Organic Reaction Mechanisms. John Wiley & Sons, Ltd., 1993. http://dx.doi.org/10.1002/9780470319543.

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Gallego, Mar Gómez, and Miguel A. Sierra. Organic Reaction Mechanisms. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-18788-9.

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Knipe, A. C., and W. E. Watts, eds. Organic Reaction Mechanisms. John Wiley & Sons, Ltd., 1985. http://dx.doi.org/10.1002/9780470066690.

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Knipe, A. C., and W. E. Watts, eds. Organic Reaction Mechanisms. John Wiley & Sons, Ltd., 1986. http://dx.doi.org/10.1002/9780470066713.

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Knipe, A. C., and W. E. Watts, eds. Organic Reaction Mechanisms. John Wiley & Sons, Ltd., 1988. http://dx.doi.org/10.1002/9780470066751.

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KNIPE, A. C., and W. E. WATTS, eds. Organic Reaction Mechanisms. John Wiley & Sons, Ltd., 1989. http://dx.doi.org/10.1002/9780470066775.

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KNIPE, A. C., and W. E. WATTS, eds. Organic Reaction Mechanisms. John Wiley & Sons, Ltd., 1990. http://dx.doi.org/10.1002/9780470066799.

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Book chapters on the topic "Organic reaction"

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Gallego, Mar Gómez, and Miguel A. Sierra. "Level 1 — Case 1 A Surprise in the Synthesis of Guanacastepene A." In Organic Reaction Mechanisms. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-18788-9_1.

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Gallego, Mar Gómez, and Miguel A. Sierra. "Level 1 — Case 10 Nucleophile Versus Base Catalysis." In Organic Reaction Mechanisms. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-18788-9_10.

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Gallego, Mar Gómez, and Miguel A. Sierra. "Level 1 — Case 11 The Hydrolysis of p-Substituted Styrene Oxides." In Organic Reaction Mechanisms. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-18788-9_11.

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Gallego, Mar Gómez, and Miguel A. Sierra. "Level 1 — Case 12 Elimination Reactions of Benzaldehyde O-Benzoyloximes." In Organic Reaction Mechanisms. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-18788-9_12.

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Gallego, Mar Gómez, and Miguel A. Sierra. "Level 1 — Case 13 Oxygen Versus Sulfur Stabilization of Carbenium Ions." In Organic Reaction Mechanisms. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-18788-9_13.

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Gallego, Mar Gómez, and Miguel A. Sierra. "Level 1 — Case 14 Cyclization of 2,3-Dibenzylidenesuccinates." In Organic Reaction Mechanisms. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-18788-9_14.

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Gallego, Mar Gómez, and Miguel A. Sierra. "Level 1 — Case 15 Oxazoline N-Oxides as Dipoles in [3+2] Cycloadditions." In Organic Reaction Mechanisms. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-18788-9_15.

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Gallego, Mar Gómez, and Miguel A. Sierra. "Level 1 — Case 16 Light-Induced Cycloadditions of N-Phthaloyl α-Amino Acids." In Organic Reaction Mechanisms. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-18788-9_16.

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Gallego, Mar Gómez, and Miguel A. Sierra. "Level 2 — Case 17 Change in Rate-Determining Step in an E1cB Mechanism: Aminolysis of Sulfamate Esters." In Organic Reaction Mechanisms. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-18788-9_17.

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Gallego, Mar Gómez, and Miguel A. Sierra. "Level 2 — Case 18 Unusual Diels-Alder Reactivity of Acyclic 2-Azadienes." In Organic Reaction Mechanisms. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-18788-9_18.

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Conference papers on the topic "Organic reaction"

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McAndrew, T. P., K. G. Frase, and R. R. Shaw. "Reaction of organic materials with YBa2Cu3Ox." In AIP Conference Proceedings Volume 165. AIP, 1988. http://dx.doi.org/10.1063/1.37078.

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Silva, Bruno Henrique Sacoman Torquato da, Lucas Michelão Martins, and Luiz Carlos da Silva-Filho. "Multicomponent Povarov reaction catalyzed by NbCl5." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0112-1.

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Chiang, Jay, and K. Sharpless. "Automation in Reaction Optimization." In The 3rd International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1999. http://dx.doi.org/10.3390/ecsoc-3-01762.

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Teixeira, Milena G., Elson S. Alvarenga, Antonio J. Demuner, Célia R. A. Maltha, and Luiz Claudio A. Barbosa. "Synthesis of isobenzofuranones by Diels-Alder reaction." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013910132953.

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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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Dudley, Gregory B., and Albert E. Stiegman. "Selective Microwave Heating of Organic Reaction Mixtures." In 2018 Asia-Pacific Microwave Conference (APMC). IEEE, 2018. http://dx.doi.org/10.23919/apmc.2018.8617572.

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Kopelman, Raoul. "Delayed Fluorescence, Reaction Kinetics And Organic Materials." In 1988 Los Angeles Symposium--O-E/LASE '88, edited by E. R. Menzel. SPIE, 1988. http://dx.doi.org/10.1117/12.945460.

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Kroutil, W., S. Mayer, and K. Faber. "Enzyme-Initiated Domino-(Cascade)-Reaction." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01912.

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Dolzhenko, Anton, Anna Dolzhenko, and Wai-Keung Chui. "Reaction of azaheterylguanidines with trichloroacetonitrile." In The 10th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2006. http://dx.doi.org/10.3390/ecsoc-10-01383.

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Carmona, Rafaela C., and Carlos Roque D. Correia. "Asymmetric Arylation of Indenes via Heck-Matsuda Reaction." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_201381992939.

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Reports on the topic "Organic reaction"

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Garrison, W. M. Reaction analogues in the radiation-induced deamination and dephosphorylation of bio-organic molecules 2: Oxygenated solutions. Office of Scientific and Technical Information (OSTI), 1988. http://dx.doi.org/10.2172/5168968.

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Roger Atkinson and Janet Arey. Studies of the Atmospheric Chemsitry of Energy-Related Volatile Organic Compounds and of their Atmospheric Reaction Products. Office of Scientific and Technical Information (OSTI), 2007. http://dx.doi.org/10.2172/902099.

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Lunsford, J., D. W. Goodman, and J. F. Haw. The adsorption and reaction of halogenated volatile organic compounds (VOC's) on metal oxides. 1998 annual progress report. Office of Scientific and Technical Information (OSTI), 1998. http://dx.doi.org/10.2172/13641.

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Postma, A. K., D. B. Bechtold, G. L. Borsheim, et al. Safety analysis of exothermic reaction hazards associated with the organic liquid layer in tank 241-C-103. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10149313.

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Lunsford, J. H., J. F. Haw, and D. W. Goodman. The adsorption and reaction of halogenated volatile organic compounds (VOC's) on metal oxides. Annual progress report, September 1996--October 1997. Office of Scientific and Technical Information (OSTI), 1997. http://dx.doi.org/10.2172/13640.

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Meacham, J. E. Ignition requirements for organic-nitrate propagating reactions. Office of Scientific and Technical Information (OSTI), 1997. http://dx.doi.org/10.2172/325381.

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Phillips, Shawn H., Rene I. Gonzalez, Rusty L. Blanski, Brent D. Viers, and Gar B. Hoflund. Hybrid Inorganic/Organic Reactive Polymers for Severe Environment Protection. Defense Technical Information Center, 2002. http://dx.doi.org/10.21236/ada410034.

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Fields, Nathan, Dennis J. Miller, Navinchandra S. Asthana, Aspi K. Kolah, Dung Vu, and Carl T. Lira. Reactive Distillation for Esterification of Bio-based Organic Acids. Office of Scientific and Technical Information (OSTI), 2008. http://dx.doi.org/10.2172/937553.

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Midey, Anthony. Ion-Molecular Reactions With Organic and Atmospheric Compounds from 150-1400K. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada405891.

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Duval, Paul, and Christopher Chancellor. Safety Evaluation of Nitric Acid Reactions with Non-Polysaccharide Organic Materials. Office of Scientific and Technical Information (OSTI), 2020. http://dx.doi.org/10.2172/1648067.

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