Relevant bibliographies by topics / 2-pyrrolidinones

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

Academic literature on the topic '2-pyrrolidinones'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "2-pyrrolidinones"

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Wei, Wen-Ting, Wei-Wei Ying, Wei-Ting Chen, et al. "Room Temperature, Metal-Free, Radical Chloroazidation of 1,6-Enynes." Synlett 29, no. 12 (2018): 1664–68. http://dx.doi.org/10.1055/s-0037-1609752.

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Without employing any transition metal, a mild, practical, and environmentally attractive methodology has been developed for the chloroazidation of 1,6-enynes at room temperature. In this radical cascade process, three new chemical bonds, including C–Cl (Br, I), C–N, and C–C bonds, are formed in one step for the construction of 2-pyrrolidinones. The method is valuable because of its mild reaction conditions, operational simplicity, and the rich biological activity of the corresponding 2-pyrrolidinone products.
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Rigo, Benoǐt, Charles Lespagnol, and Marc Pauly. "Studies on pyrrolidinones. A convenient synthesis of 5-cyano-2-pyrrolidinone derivatives." Journal of Heterocyclic Chemistry 23, no. 1 (1986): 183–84. http://dx.doi.org/10.1002/jhet.5570230137.

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Ruostesuo, P., and P. Piril�-Honkanen. "Thermodynamic and spectroscopic properties of 2-pyrrolidinones. 2. Dielectric properties of 2-pyrrolidinone in binary mixtures." Journal of Solution Chemistry 19, no. 5 (1990): 473–82. http://dx.doi.org/10.1007/bf00650380.

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Ghelfi, Franco, Gianluca Ghirardini, Emanuela Libertini, Luca Forti, and Ugo M. Pagnoni. "Easy approach to 3-benzylimino-2-pyrrolidinones from 3-chloro-4-chloromethyl-2-pyrrolidinones." Tetrahedron Letters 40, no. 49 (1999): 8595–97. http://dx.doi.org/10.1016/s0040-4039(99)01798-0.

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Breinbauer, Rolf, Marko Kljajic, and Thomas Schlatzer. "Synthesis of 2-Pyrrolidinones by Palladium-Catalyzed [3+2] Cycloaddition of Isocyanates." Synlett 30, no. 05 (2019): 581–85. http://dx.doi.org/10.1055/s-0037-1610692.

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Pd/DPEphos catalyzes the [3+2] cycloaddition of various alkyl isocyanates with 2-acetoxymethyl-3-allyltrimethylsilane as a synthetic equivalent of trimethylenemethane (TMM). Taking advantage of 2-acetoxymethyl-3-allyltrimethylsilane acting both as nucleophile as well as electrophile this reaction gives a convenient access to 5-ring lactams with an exocyclic alkene moiety. The formation of the β,γ-unsaturated 2-pyrrolidinones occurs without olefin isomerization and without epimerization of the stereogenic centers. Mechanistic investigations suggest an initial N-allylation of the isocyanate foll
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Zav'yalov, S. I., and N. E. Kravchenko. "Synthesis of 5-alkylidene-2-pyrrolidinones." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 38, no. 5 (1989): 1087–90. http://dx.doi.org/10.1007/bf00955460.

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Ghelfi, Franco, Gianluca Ghirardini, Emanuela Libertini, Luca Forti, and Ugo M. Pagnoni. "ChemInform Abstract: Easy Approach to 3-Benzylimino-2-pyrrolidinones from 3-Chloro-4-chloromethyl-2-pyrrolidinones." ChemInform 31, no. 9 (2010): no. http://dx.doi.org/10.1002/chin.200009117.

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Ruostesuo, P., P. Pirilä-Honkanen, and L. Heikkinen. "Thermodynamic and spectroscopic properties of 2-pyrrolidinones. 3. NMR spectroscopic studies on 2-pyrrolidinone in different solvents." Journal of Physical Organic Chemistry 2, no. 7 (1989): 565–72. http://dx.doi.org/10.1002/poc.610020709.

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Moutevelis-Minakakis, Panagiota, Eleni Papavassilopoulou, and Thomas Mavromoustakos. "Synthesis of New Optically Active 2-Pyrrolidinones." Molecules 18, no. 1 (2012): 50–73. http://dx.doi.org/10.3390/molecules18010050.

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Zaragoza-Galicia, Ivann, Zaira A. Santos-Sánchez, Yazmín I. Hidalgo-Mercado, Horacio F. Olivo, and Moisés Romero-Ortega. "Synthesis of 5-Substituted 2-Pyrrolidinones by Coupling of Organozinc Reagents with Cyclic N-Acyliminium Ions." Synthesis 51, no. 24 (2019): 4650–56. http://dx.doi.org/10.1055/s-0037-1610733.

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A coupling reaction between cyclic N-acyliminium ions with organozinc reagents is described. The cyclic N-acyliminium ions, generated in situ from N-substituted-5-hydroxy-2-pyrrolidinones by treatment with boron trifluoride–diethyl ether complex or titanium tetrachloride, are trapped by the organozinc reagent, which is formed from an alkyl bromide in the presence of zinc in the same reaction medium. The N-substituted-5-allyl-2-pyrrolidinones generated using this method serve as versatile intermediates for the synthesis of azabicyclic systems with indolizidine and pyrroloazepinolizidine cores.
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Dissertations / Theses on the topic "2-pyrrolidinones"

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Ferreira, Fernando da Paz [UNIFESP]. "Adição Nucleofílica de Sais de Potássio de Organotrifluoroboratos à Íons N-Acilimínio." Universidade Federal de São Paulo (UNIFESP), 2009. http://repositorio.unifesp.br/handle/11600/8875.

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Made available in DSpace on 2015-07-22T20:49:18Z (GMT). No. of bitstreams: 0 Previous issue date: 2009-06-24. Added 1 bitstream(s) on 2015-08-11T03:25:29Z : No. of bitstreams: 1 Publico-00299a.pdf: 807068 bytes, checksum: e4fb701e403dec161fff1eb2278518d5 (MD5). Added 1 bitstream(s) on 2015-08-11T03:25:29Z : No. of bitstreams: 2 Publico-00299a.pdf: 807068 bytes, checksum: e4fb701e403dec161fff1eb2278518d5 (MD5) Publico-00299b.pdf: 1749779 bytes, checksum: d8cc731e3f8410ce7bdb335a435143ec (MD5)<br>Neste trabalho, desenvolvemos uma nova metodologia para a obtencao estereosseletiva de pirroli
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Chou, Tai-Li. "Kinetics of salt formation using terephthalic acid and N-methyl-2-pyrrolidinone." Thesis, Montana State University, 2004. http://etd.lib.montana.edu/etd/2004/chou/ChouT04.pdf.

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Terephthalic acid (TA) is used as a raw material for producing polyesters. As the global demand for polyesters increases at a rate of 7% per year on average for the last few years and next 10-year forecast, the demand of TA also increases. The global production exceeded 27 million tons for the year 2003, and will be in excess of 30 million tons for the year 2004. Therefore improving the production or purification process for terephthalic acid becomes more and more important. A new purification method using N-methyl-2-pyrrolidinone (NMP) as solvent was recently developed. In this process, the s
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EL, ALAMI NAJAT. "Isolement et reactivite du derive zincique de (bromomethyl-2) acrylate d'ethyle : synthese de methylene-3 pyrrolidinone-3 potentiellement antineoplasique." Nantes, 1987. http://www.theses.fr/1987NANT2016.

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Reaction de l'organozinicique allylique prepare, avec divers electrophiles conduisant a des methylene-3 perhydrofurannones-2 et -pyrrolidones-2. Etude de l'activite de ces composes sur la leucamie p388
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Li, Pingyen, and 李秉諺. "Densities and Viscosities of multi components mixture (Ethanol, Dimthylsulfoxide, 1-Methyl-2-pyrrolidinone)." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/9hdq3m.

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碩士<br>中國文化大學<br>化學工程與材料工程學系奈米材料碩士班<br>101<br>In the general chemical industry, the unit operation device such as extraction columns, filters and packed absorption towers; the technical area such as the synthesis reaction and separation technology, during the transports, program designs and the operations of the processes, many the characteristics of the material physical change and the phenomenon of fluid are still required to do a detailed and accurate calculation of the density and viscosity. These references are the essential elements. This work measures (ethanol + dimethylsulfoxide ), (eth
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Books on the topic "2-pyrrolidinones"

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Pirilä-Honkanen, Päivi. Physicochemical properties of 2-pyrrolidinone and n-methylbenzenesulfonamide in binary solution mixtures. Oulun Yliopisto, 1996.

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World Health Organization (WHO). N-methyl-2-pyrrolidone (Concise International Chemical Assessment Document). World Health Organization, 2003.

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Book chapters on the topic "2-pyrrolidinones"

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Knaup, Guenter, Karlheinz Drauz, and Michael Schwarm. "O-Acetyl-L-homoserine: A versatile synthon for the synthesis of L-homoserine peptides and 3-amino-2-pyrrolidinones." In Peptides for the New Millennium. Springer Netherlands, 2002. http://dx.doi.org/10.1007/0-306-46881-6_23.

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Gooch, Jan W. "1-Methyl-2-Pyrrolidinone (NMP)." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_7436.

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Liu, Yan, Tianyi Shang, Zhong Chen, et al. "A Concise and Diversity-Oriented Strategy for the Synthesis of Substituted 2-Pyrrolidinones via an Ugi/Intramolecular Inverse Electron Demand Diels-Alder Sequence." In Lecture Notes in Electrical Engineering. Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-4801-2_42.

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Wohlfarth, Ch. "Solubility parameter of poly(1-vinyl-2-pyrrolidinone)." In Polymer Solutions. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02890-8_1031.

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Wohlfarth, Ch. "High pressure fluid phase equilibrium data of poly(1-vinyl-2-pyrrolidinone) in carbon dioxide and 1-methyl-2-pyrrolidinone." In Polymer Solutions. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-32057-6_303.

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Wohlfarth, Ch. "Partial specific volume of poly(1-vinyl-2-pyrrolidinone)." In Polymer Solutions. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02890-8_312.

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Wohlfarth, Ch. "Second virial coefficient of poly(1-vinyl-2-pyrrolidinone)." In Polymer Solutions. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02890-8_752.

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Hirota, E., K. Kuchitsu, T. Steimle, J. Vogt, and N. Vogt. "189 C10H12N2O (5S)-1-Methyl-5-(3-pyridinyl)-2-pyrrolidinone." In Molecules Containing Three or Four Carbon Atoms and Molecules Containing Five or More Carbon Atoms. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-41504-3_320.

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Wohlfarth, Ch. "pVT data of poly(1-vinyl-2-pyrrolidinone) in dimethylsulfoxide." In Polymer Solutions. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02890-8_144.

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Wohlfarth, Ch. "pVT data of poly(1-vinyl-2-pyrrolidinone) in ethanol." In Polymer Solutions. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-02890-8_145.

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Conference papers on the topic "2-pyrrolidinones"

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Dallas, Andrew J., Lefei Ding, Jon Joriman, Brian Hoang, Kevin Seguin, and Dustin Zastera. "An investigation of the removal of 1-Methyl-2-Pyrrolidinone (NMP)." In SPIE 31st International Symposium on Advanced Lithography, edited by Chas N. Archie. SPIE, 2006. http://dx.doi.org/10.1117/12.654839.

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Gerlach, Carina, and Olfa Kanoun. "Optimization of Ultrasonic Parameters for Deagglomeration of Carbon Nanotubes Within 1-Methy1-2-Pyrrolidinone (NMP) Dispersion." In 2016 Nanotechnology for Instrumentation and Measurement (NANOfIM). IEEE, 2016. http://dx.doi.org/10.1109/nanofim.2016.8521427.

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Najera, Carmen, Tomas Abellan, Diego Alonso, et al. "(S)-5-(Tosylmethyl)-2-pyrrolidinone: A New Chiral b -Amidosulfone for a Short Asymmetric Synthesis of Indolizidines." In The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01811.

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Chen, Chang-hsiu, John LaRue, and Richard Nelson. "Materials Properties of Polymer Blends of Poly(3,4-ethlenedioxythiophene)/Poly(styrenesulfonate)/N-Methyl-2-pyrrolidinone (PEDOT:PSS:NMP) and Polyvinyl Alcohol (PVA." In 2008 MRS Fall Meetin. Materials Research Society, 2008. http://dx.doi.org/10.1557/proc-1134-bb05-41.

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Damas, Sara M., and Cameron J. Turner. "The Material Testing of Nanoparticle Doped 3D Printed ABS Strain Gages for Resisitance and Stiffness." In ASME 2020 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. American Society of Mechanical Engineers, 2020. http://dx.doi.org/10.1115/detc2020-22542.

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Abstract Additive manufacturing methods are becoming more prominent in the world of design and manufacturing due to their reduction of material waste versus traditional machining methods such as milling. The technology to 3D print has been around since the 1970’s. In today’s present time, we now can multi-material 3D print, however. even though we have the technology for multi-material 3D printing, standards in this field are severely lacking. Research on multi-material 3D printing and/or the combination of 3D printing filaments combined with nanoparticles is needed. One of the most common met
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