Relevant bibliographies by topics / Amino catalyst

Contents

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

Academic literature on the topic 'Amino catalyst'

Author: Grafiati
Published: 4 June 2021
Last updated: 8 February 2022

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Journal articles on the topic "Amino catalyst"

1

Hill, C. A. S., N. S. Cetin, and N. Ozmen. "Potential Catalysts for the Acetylation of Wood." Holzforschung 54, no. 3 (2000): 269–72. http://dx.doi.org/10.1515/hf.2000.045.

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Summary The potential of several tertiary amine catalysts (pyridine, 4-dimethyl-amino pyridine, N-methyl pyrrolidine and N-methyl pyrrolidinone) for the acetylation of Corsican pine sapwood, using acetic anhydride, has been investigated. Rates of reaction were compared with non-catalysed acetylation using acetic anhydride. The hypernucleophile 4-dimethylamino pyridine was found to be the most effective catalyst of those studied. At a concentration of only 1% of the catalyst in acetic anhydride, a weight percent gain of 20% was realised, compared with 7% for the uncatalysed reaction, after 30 m
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Parasuraman, Perumalsamy, Zubeda Begum, Madhu Chennapuram, et al. "Simple organocatalyst component system for asymmetric hetero Diels–Alder reaction of isatins with enones." RSC Advances 10, no. 30 (2020): 17486–91. http://dx.doi.org/10.1039/d0ra03006f.

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A simple two catalysts component system of β-amino alcohols (catalyst) and amino acids (co-catalyst) works as an efficient organocatalysts in hetero Diels–Alder reaction of isatins with enones to afford chiral spirooxindole-tetrahydropyranones.
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Chabolla, S. A., C. W. Machan, J. Yin, et al. "Bio-inspired CO2reduction by a rhenium tricarbonyl bipyridine-based catalyst appended to amino acids and peptidic platforms: incorporating proton relays and hydrogen-bonding functional groups." Faraday Discussions 198 (2017): 279–300. http://dx.doi.org/10.1039/c7fd00003k.

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Herein, we report a new approach to bio-inspired catalyst design. The molecular catalyst employed in these studies is based on the robust and selective Re(bpy)(CO)<sub>3</sub>Cl-type (bpy = 2,2′-bipyridine) homogeneous catalysts, which have been extensively studied for their ability to reduce CO<sub>2</sub>electrochemically or photochemically in the presence of a photosensitizer. These catalysts can be highly active photocatalysts in their own right. In this work, the bipyridine ligand was modified with amino acids and synthetic peptides. These results build on earlier findings wherein the bip
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Latypova, Adele R., Maxim D. Lebedev, Evgeniy V. Rumyantsev, et al. "Amino-Modified Silica as Effective Support of the Palladium Catalyst for 4-Nitroaniline Hydrogenation." Catalysts 10, no. 4 (2020): 375. http://dx.doi.org/10.3390/catal10040375.

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The article describes the synthesis of aminoorgano-functionalized silica as a prospective material for catalysis application. The amino groups have electron donor properties which are valuable for the metal chemical state of palladium. Therefore, the presence of electron donor groups is important for increasing catalysts’ stability. The research is devoted to the investigation of silica amino-modified support influence on the activity and stability of palladium species in 4-nitroaniline hydrogenation process. A series of catalysts with different supports such as SiO2, SiO2-C3H6-NH2 (amino-func
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Fadlalla, Mohamed, Glenn Maguire, and Holger Friedrich. "The Heterogeneous Aminohydroxylation Reaction Using Hydrotalcite-Like Catalysts Containing Osmium." Catalysts 8, no. 11 (2018): 547. http://dx.doi.org/10.3390/catal8110547.

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The aminohydroxylation reaction of olefins is a key organic transformation reaction, typically carried out homogeneously with toxic and expensive osmium (Os) catalysts. Therefore, heterogenisation of this reaction can unlock its industrial potential by allowing reusability of the catalyst. Os–Zn–Al hydrotalcite-like compounds (HTlcs), as potential heterogeneous aminohydroxylation catalysts, were synthesised by the co-precipitation method and characterised by several techniques. Reaction parameters (i.e., solvent system, reaction temperature, and catalyst structure) were optimized with cyclohex
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Michrowska, Anna, and Karol Grela. "Quest for the ideal olefin metathesis catalyst." Pure and Applied Chemistry 80, no. 1 (2008): 31–43. http://dx.doi.org/10.1351/pac200880010031.

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Attempts were made to create a catalyst that approaches Gladysz's vision of an "ideal catalyst". Modifications of the Hoveyda-Grubbs catalyst were carried out with the aim to increase its activity and broaden the scope of its applicability to challenging metathesis reactions. This was done by introduction of an electron-withdrawing substituent on the isopropoxybenzylidene group in order to diminish the donor properties of the oxygen atom. The resulting stable and easily accessible nitro-substituted Hoveyda-Grubbs catalyst has found a number of successful applications in various research and in
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Kim, Seonghee, Hyun Park, and Oi Lun Li. "Cobalt Nanoparticles on Plasma-Controlled Nitrogen-Doped Carbon as High-Performance ORR Electrocatalyst for Primary Zn-Air Battery." Nanomaterials 10, no. 2 (2020): 223. http://dx.doi.org/10.3390/nano10020223.

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Metal–air batteries and fuel cells have attracted much attention as powerful candidates for a renewable energy conversion system for the last few decades. However, the high cost and low durability of platinum-based catalysts used to enhance sluggish oxygen reduction reaction (ORR) at air electrodes prevents its wide application to industry. In this work, we applied a plasma process to synthesize cobalt nanoparticles catalysts on nitrogen-doped carbon support with controllable quaternary-N and amino-N structure. In the electrochemical test, the quaternary-N and amino-N-doped carbon (Q-A)/Co cat
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Al-Harbi, Laila M., Manal M. Khowdiary, H. S. Nassar, et al. "Experimental and theoretical investigation to improvement biodiesel production using green catalyst based on cellulose derivatives." Materials Express 11, no. 1 (2021): 142–51. http://dx.doi.org/10.1166/mex.2021.1876.

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The present study aimed to enhancement production of the biodiesel process using new green catalyst. The obtained compounds were established using diverse spectroscopic data. These molecules were evaluated as catalyst in production process. The biodiesel yield was 93% in case of copper complex catalyst, while the amino acid catalyst give 96% yield. To get clear insight for catalysts properties, we measured surface activity and simulating the chemical reactivity using HF quantum calculation. The obtained data summarize that using the prepared catalyst lowering the biodiesel process cost through
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Depreux, P., and A. Marcincal-Lefebvre. "Application des conditions de réaction par transfert de phase à la synthèse d'amino-éthers dérivés du trans phénoxy-2 cyclohexanol." Canadian Journal of Chemistry 64, no. 3 (1986): 626–32. http://dx.doi.org/10.1139/v86-101.

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Amino-ethers of trans-2-phenoxycyclohexanol were prepared by methods involving anhydrous conditions (sodium alkoxides in xylene) or phase transfer catalysis conditions (liquid–liquid or solid–liquid two-phase systems). Various factors were optimized. In the liquid–liquid two-phase system, when no catalyst was added, reaction proceeds with comparable or even better yields than with some PTC catalysts, a quaternary salt being formed insitu. It was shown that the deprotonation of ROH takes place at the interface, since there was no OH− extraction in organic medium and the yield depends on the sti
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Guo, Hong Qi, Gong Yan, Ming Qing Chen, and Shi Rong Liu. "Assembling of 12-Tungstophosphoric Acid into Amino-Modified SBA-15 and its Catalytic Performance." Advanced Materials Research 465 (February 2012): 224–28. http://dx.doi.org/10.4028/www.scientific.net/amr.465.224.

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12-tungstophosphoric acid was supported on amine-modified SBA-15 by impregnation. The structure and properties of the catalyst were characterized by FT-IR spectroscopy, X-ray diffraction, N2 adsorption-desorption, TEM,Raman spectra and NH3–TPD technology.the result confirmed the mesostructure for SBA-15 and the Keggin structure of the heteropolyanions was preserved. The tungstophosphoric acid can disperse in the pore of the support SBA-15/NH2, but the acidity of the catalyst reduced. The catalytic activities of the catalysts were evaluated for the esterification reaction of ethyl acetoacetate
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Dissertations / Theses on the topic "Amino catalyst"

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Silverio, Daniel L. "Development of Amino Acid-Derived Ligands for Enantioselective Synthesis of Amines and Alcohols." Thesis, Boston College, 2014. http://hdl.handle.net/2345/bc-ir:104413.

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Thesis advisor: Amir H. Hoveyda<br>Chapter One Development of Simple Organic Molecules as Catalysts for Enantioselective Allyl Additions to N-Phosphinoylaldimines and Isatins A new catalytic protocol for the enantioselective addition of organoborates to imines and carbonyls is described. This novel method, which does not require transition metals utilizes a modular and easily accessed aminophenol to dictate the stereochemistry of the products. Allyl-additions to N-phosphinoylaldimines and isatins, as well as allenyl-additions to isatins are studied and literature relevant to these transformati
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Ahlford, Katrin. "Asymmetric transfer hydrogenation of ketones : Catalyst development and mechanistic investigation." Doctoral thesis, Stockholms universitet, Institutionen för organisk kemi, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-55412.

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The development of ligands derived from natural amino acids for asymmetric transfer hydrogenation (ATH) of prochiral ketones is described herein. In the first part, reductions performed in alcoholic media are examined, where it is found that amino acid-derived hydroxamic acids and thioamides, respectively, are simple and versatile ligands that in combination with [RhCp*Cl2]2 efficiently catalyze this particular transformation. Selectivities up to 97% ee of the corresponding secondary alcohols are obtained, and it is furthermore observed that the two different ligand classes, albeit based on th
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Ogata, Kazuki. "Syntheses and Functions of Metalated Amino Acids and Peptides." 京都大学 (Kyoto University), 2012. http://hdl.handle.net/2433/158074.

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Larsen, Catharine Hoang-Mai MacMillan David W. C. Barton Jacqueline K. "Investigating imidazolidinone catalysts : enantioselective organocatalytic Diels-Alder reactions, conjugate additions to access non-natural alpha-amino acids, and bimodal catalyst activation for the development of organo-cascade reactions /." Diss., Pasadena, Calif. : California Institute of Technology, 2006. http://resolver.caltech.edu/CaltechETD:etd-10142005-105810.

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Dangel, Brian Douglas. "Efforts towards the development of a universal catalyst system: Transition metal complexes derived from O'Donnell Schiff bases of amino acids." Diss., The University of Arizona, 2000. http://hdl.handle.net/10150/289212.

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Given the success of organic ligands in transition metal catalysis, we incorporated the chirality of amino acids into new ligands for asymmetric catalysis. Moreover, it was hoped that through the incorporation of the bulky benzophenone imine moieties (-N=CPh₂), that the "pendant chirality" of the amino acids could be reflected in the "central chirality" about the transition metal. An achiral diamine serves to bring two optically active amino acid residues in close proximity to form an "active site." The two amido and two imine-nitrogens have been shown to bind Ni(II) in a square planar fashion
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Martins, Rafaela de Souza. "Preparação e utilização de amino catalisadores - derivados do glicerol, D-manitol e L-aminoácidos - em reações de adição aldólica." Universidade Federal de Juiz de Fora (UFJF), 2017. https://repositorio.ufjf.br/jspui/handle/ufjf/5876.

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Submitted by Renata Lopes (renatasil82@gmail.com) on 2017-10-10T11:51:05Z No. of bitstreams: 1 rafaeladesouzamartins.pdf: 11994443 bytes, checksum: c42e2d285fd87e325b038e9bfe95bdf5 (MD5)<br>Approved for entry into archive by Adriana Oliveira (adriana.oliveira@ufjf.edu.br) on 2017-10-10T12:22:21Z (GMT) No. of bitstreams: 1 rafaeladesouzamartins.pdf: 11994443 bytes, checksum: c42e2d285fd87e325b038e9bfe95bdf5 (MD5)<br>Made available in DSpace on 2017-10-10T12:22:21Z (GMT). No. of bitstreams: 1 rafaeladesouzamartins.pdf: 11994443 bytes, checksum: c42e2d285fd87e325b038e9bfe95bdf5 (MD5) Previous i
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Birepinte, Mélodie. "Amino(organo)boranes, synthèse et propriétés." Thesis, Bordeaux, 2019. http://www.theses.fr/2019BORD0231.

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Ce manuscrit présente la synthèse, la réactivité et les propriétés des amino(organo)boranes. Le diisopropylaminoborane a été utilisé dans le cadre de la formation de liaisons carbone-bore. La réactivité du diisopropylaminoborane en tant qu’agent de borylation a d’abord été mise à profit pour l’hydroboration des alcynes catalysée par le réactif de Schwartz. Une grande variété d’alcénylaminoboranes, -boronates et -diazaborolanes a ainsi été synthétisée. Leur transformation stéréosélective en bromoalcènes Z et E a également été optimisée. La borylation des alcynes vrais via un procédé tandem de d
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Tabanella, Stefania. "Pyridyl-amino acids for potential catalysts." Thesis, University of Sheffield, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.269279.

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Teoh, Euneace Ching Mei. "Synthesis of amino acids by metal-catalysed reactions." Monash University, School of Chemistry, 2004. http://arrow.monash.edu.au/hdl/1959.1/9633.

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Zhang, Yin. "Backbone decoration of imidazol-2-ylidene ligands with amino groups and their application in palladium catalyzed arylative amination reaction." Thesis, Toulouse 3, 2015. http://www.theses.fr/2015TOU30109/document.

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Ce travail s'inscrit dans le cadre de la chimie des carbènes N-hétérocycliques (NHC) et s'articule autour de la fonctionnalisation directe de l'hétérocycle des l'imidazol-2-ylidènes par substitution formelle d'un ou deux groupements diméthylamino. Deux nouvelles catégories de NHCs ont d'abord été obtenues par cette stratégie, dénommées 4-(diméthylamino)imidazol-2-ylidène IArNMe2 et 4,5-bis(diméthylamino)imidazol-2-ylidène IAr(NMe2)2. Les sels d'imidazolium précurseurs de ces NHCs, à savoir le triflate de 4-(diméthylamino)imidazolium (IArNMe2)·HOTf et le triflate de 4,5-bis(diméthylamino)imidaz
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Books on the topic "Amino catalyst"

1

Milne, John Joseph. A study of tryptophan synthase catalysed hydrogen-deuterium exchange reactions. University College Dublin, 1996.

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Fitzpatrick, Teresa. Studies on the serine hydroxymethyltransferase catalysed exchange of the [alpha]-protons of amino acids. University College Dublin, 1998.

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Hughes, Andrew B. Amino acids, peptides and proteins in organic chemistry: Building blocks, catalysis and coupling chemistry. Wiley-VCH, 2011.

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A, Łukasiewicz, ed. New surface layer materials from polymetallic aminotriazole complexes on various supports. Institute of Nuclear Chemistry and Technology, 1994.

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I͡A︡, Lukevit͡s︡ Ė, Birgele Irena Stanislavovna, and Organiskās sintēzes institūts (Latvijas PSR Zinātn̦u akadēmija), eds. Kremniĭorganicheskie proizvodnye aminospirtov: Fiziko-khimicheskie issledovanii͡a︡. "Zinatne", 1987.

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R, Hill Aubrey, and Orgel Leslie E, eds. Catalysis of the oligomerization of o-phospho-serine, aspartic acid, or glutamic acid by cationic micelles. National Aeronautics and Space Administration, 1997.

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Jumnah, Roshan. Palladium catalysed allylic amination in the formation of a-amino acids. 1995.

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Hughes, Andrew B. Amino Acids, Peptides and Proteins in Organic Chemistry, Building Blocks, Catalysis and Coupling Chemistry. Wiley & Sons, Incorporated, John, 2011.

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Hughes, Andrew B. Amino Acids, Peptides and Proteins in Organic Chemistry, Building Blocks, Catalysis and Coupling Chemistry. Wiley & Sons, Incorporated, John, 2011.

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Hughes, Andrew B. Amino Acids, Peptides and Proteins in Organic Chemistry, Building Blocks, Catalysis and Coupling Chemistry Vol. 3. Wiley & Sons, Incorporated, John, 2011.

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Book chapters on the topic "Amino catalyst"

1

Ager, David, Michel van den Berg, Adriaan J. Minnaard, et al. "An Affordable Catalyst for the Production of Amino Acids." In ACS Symposium Series. American Chemical Society, 2004. http://dx.doi.org/10.1021/bk-2004-0880.ch008.

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Brazier, John B., and Nicholas C. O. Tomkinson. "Secondary and Primary Amine Catalysts for Iminium Catalysis." In Topics in Current Chemistry. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/128_2008_28.

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Brazier, John B., and Nicholas C. O. Tomkinson. "Secondary and Primary Amine Catalysts for Iminium Catalysis." In Topics in Current Chemistry. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-02815-1_28.

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Xu, Li-Wen, and Yixin Lu. "Non-Proline Amino Acid Catalysts." In Comprehensive Enantioselective Organocatalysis. Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527658862.ch3.

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Terada, Masahiro, and Norie Momiyama. "Enantioselective Synthesis of Amines by Chiral Brønsted Acid Catalysts." In Chiral Amine Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527629541.ch3.

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Chen, Liujuan, and Sanzhong Luo. "Chiral Primary Amine Catalysis." In Enantioselective Organocatalyzed Reactions I. Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-90-481-3865-4_5.

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Illanes, Andrés, Fanny Guzmán, and Sonia Barberis. "Proteases as Powerful Catalysts for Organic Synthesis." In Amino Acids, Peptides and Proteins in Organic Chemistry. Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527631780.ch8.

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Xie, Haibo, Thomas Hayes, and Nicholas Gathergood. "Catalysis of Reactions by Amino Acids." In Amino Acids, Peptides and Proteins in Organic Chemistry. Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527631780.ch7.

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Punekar, N. S. "Electrophilic Catalysis and Amino Acid Transformations." In ENZYMES: Catalysis, Kinetics and Mechanisms. Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-13-0785-0_35.

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Wenzel, Anna G., та Eric N. Jacobsen. "Asymmetric Catalysis in Enantioselective Synthesis of β-Amino Acids". У Enantioselective Synthesis of β-Amino Acids. John Wiley & Sons, Inc., 2005. http://dx.doi.org/10.1002/0471698482.ch4.

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Conference papers on the topic "Amino catalyst"

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Javanshir, Shahrzad, and Mohammad Farhadnia. "Cellulose-Supported Metal Nanocomposite as a Green and Reusable Catalyst for One-Pot Multicomponent Synthesis of 2-Amino-4H-Chromene Derivatives." In The 18th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a019.

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Córdova, Armando, Enrique Díaz-Herrera, and Eusebio Juaristi. "Asymmetric Amino Acid Catalysis." In 2007. AIP, 2008. http://dx.doi.org/10.1063/1.2901846.

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Cahyana, A. H., S. Saidah, and B. Ardiansah. "Nano CuFe2O4: A reusable magnetic catalyst for the synthesis of 2-amino-5,10-dioxo-4-styryl-5,10-dihydro-4H-benzo[g]chromene-3-carbonitrile via a one-pot multicomponent reaction." In PROCEEDINGS OF THE 3RD INTERNATIONAL SYMPOSIUM ON CURRENT PROGRESS IN MATHEMATICS AND SCIENCES 2017 (ISCPMS2017). Author(s), 2018. http://dx.doi.org/10.1063/1.5064072.

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Ruiduan, Li, Liu Ling, Liu Yanjie, Wang Ben, Yang Jia Jun, and Zhang Jibo. "RESEARCH PROGRESS OF AMINE CATALYSTS FOR POLYURETHANE." In International Conference on New Materials and Intelligent Manufacturing. Volkson Press, 2018. http://dx.doi.org/10.26480/icnmim.01.2018.54.57.

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Sungail, Craig. "Amino Acid Salts - A New Family of Semi-Rigid Polyurethane Catalysts." In International Congress & Exposition. SAE International, 1995. http://dx.doi.org/10.4271/950864.

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Higgins, Daniel, Keith Hohn, and Abdulhafiz Usman. "Single-Molecule Fluorescence Spectroscopy Studies of the Microenvironment of Graded Amine-Functionalized Silica Surfaces." In 1st International Electronic Conference on Catalysis Sciences. MDPI, 2020. http://dx.doi.org/10.3390/eccs2020-07607.

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Mikhailov, Stepan, Mikhail Sulman, Valentina Matveeva, Alexander Sidorov, and Valentin Doluda. "N-METHYL-D-GLUCOSE AMINE SYNTHESIS OVER NI BASED CATALYSTS." In 20th International Multidisciplinary Scientific GeoConference Proceedings SGEM 2020. STEF92 Technology, 2020. http://dx.doi.org/10.5593/sgem2020/4.1/s17.016.

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Cahard, Dominique, Baptiste Thierry, and Jean-Christophe Plaquevent. "New Chiral Phase Transfer Supported Catalysts in The Asymmetric Synthesis of a -Amino Acids : The Importance of a Spacer." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01812.

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Dinh Thanh, Nguyen, Do Son Hai, Vu Thi Tuyet Thuy, Do Tien Tung, Cao Thi Le, and Hoang Thi Kim Van. "CATALYSIS INVESTIGATION FOR SYNTHESIS OF 2-AMINO-4H-PYRAN-3-CARBONITRILES CONTAINING PROPARGYL GROUP." In The 21st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04769.

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Zapata-Romero, Gilberto A., Markus Doerr, and Martha C. Daza. "Enantioselective lipase-catalyzed O-acylation of (RS)-propranolol: analysis of the hydrogen bonds essential for catalysis." In VIII Simpósio de Estrutura Eletrônica e Dinâmica Molecular. Universidade de Brasília, 2020. http://dx.doi.org/10.21826/viiiseedmol2020131.

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We investigated the effect of the acyl group size in the enantioselectivity of the acylation of propranolol, an amino alcohol used as β-adrenergic blocking agent. We applied a methodology frequently used to model enantioselectivity that is based on the hydrogen bonds present in the tetrahedral intermediate, which occurs in lipase-catalyzed reactions. We sampled the conformations of the tetrahedral intermediate corresponding to the esterification of both enantiomers of propranolol with ethanoyl and butanoyl, employing molecular dynamics simulation together with a quantum mechanics/molecular mec
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