Academic literature on the topic 'Imidazolidine-2'

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Journal articles on the topic "Imidazolidine-2"

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Sultana, Razia, Tarlok S. Lobana, and Alfonso Castineiras. "Chemistry of heterocyclic-2-thiones: in situ generated 1-(4,5-dihydro-3-alkyl-imidazolidin-2-yl)-3-alkyl-imidazolidine-2-thione and triiodide form novel mixed valent CuI–II/CuII complexes." RSC Advances 5, no. 122 (2015): 100579–88. http://dx.doi.org/10.1039/c5ra20449f.

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Copper(i) iodide transforms N-n-butyl-imidazolidine-2-thione in air into 1-(4,5-dihydro-3-butyl-imidazolidin-2-yl)-3-butyl-imidazolidine-2-thione (L-NBu<sup>n</sup>) which formed novel complex, [Cu(κ<sup>2</sup>-N,S-L-NBu<sup>n</sup>)<sub>2</sub>](I<sub>3</sub>)<sub>2</sub>.
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Vaughan, Keith, Shasta Lee Moser, Reid Tingley, M. Brad Peori, and Valerio Bertolasi. "Triazene derivatives of (1,x-)diazacycloalkanes. Part VI. 3-({5,5-Dimethyl-3-[2-aryl-1-diazenyl]-1-imidazolidinyl}methyl)-4,4-dimethyl-1-[2-aryl-1-diazenyl]imidazolidines — Synthesis, characterization, and X-ray crystal structure." Canadian Journal of Chemistry 84, no. 10 (2006): 1294–300. http://dx.doi.org/10.1139/v06-091.

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Reaction of a series of diazonium salts with a mixture of formaldehyde and 1,2-diamino-2-methylpropane affords the 3-({5,5-dimethyl-3-[2-aryl-1-diazenyl]-1-imidazolidinyl}methyl)-4,4-dimethyl-1-[2-aryl-1-diazenyl]imidazolidines (1a–1f) in excellent yield. The products have been characterized by IR and NMR spectroscopic analysis, elemental analysis, and X-ray crystallography. The X-ray crystal structure of the p-methoxycarbonyl derivative (1c) establishes without question the connectivity of these novel molecules, which can be described as linear bicyclic oligomers with two imidazolidinyl group
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Lee, See, Ainnul Azizan, and Edward Tiekink. "1-(2-Hydroxyethyl)imidazolidine-2-thione." Molbank 2018, no. 4 (2018): M1035. http://dx.doi.org/10.3390/m1035.

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1-(2-Hydroxyethyl)imidazolidine-2-thione (1) was obtained as a product from an in situ reaction between N-(2-hydroxyethyl)ethylenediamine, carbon disulfide, potassium hydroxide, and di(4-fluorobenzyl)tin dichloride. Compound 1 was characterized by IR, UV, 1H, 13C{1H}, and 2D (COSY, NOESY, HSQC, and HMBC) NMR spectroscopies. The cyclic molecular structure was confirmed by single crystal X-ray crystallography which showed the five-membered ring to be non-planar and the π-electron density to be localized over the CN2S chromophore. In the crystal, thioamide–N–H…O(hydroxy) and hydroxy–O–H…S(thione)
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Wazeer, Mohamed I. M., Anvarhusein A. Isab, and Ali El-Rayyes. "Solid state NMR study of 1,3imidazolidine-2-thione, 1,3-imidazolidine-2-selenone and some of their N-substituted derivatives." Spectroscopy 18, no. 1 (2004): 113–19. http://dx.doi.org/10.1155/2004/309130.

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Solid‒state NMR spectra were recorded for 1,3-imidazolidine-2-thione, 1,3-imidazolidine-2-selenone and some of their N-substituted derivatives. Spinning side-bands of thione and selenone carbons were analysed to yield chemical shift anisotropies for these carbons. The NMR spectrum of imidazolidine-2-thione (Imt) showed some evidence for the presence of thiol tautomer. Molecular computations were carried out for Imt and its N-methyl derivative to yield relative energies of various tautomers.
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Bjernemose, Jens K., Christine J. McKenzie, and Martin N. Mortensen. "2-Phenyl-1,3-bis(2-pyridylmethyl)imidazolidine." Acta Crystallographica Section E Structure Reports Online 59, no. 7 (2003): o1017—o1018. http://dx.doi.org/10.1107/s1600536803013394.

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Żesławska, Ewa, Ewa Szymańska, Wojciech Nitek, and Jadwiga Handzlik. "Crystallographic studies of piperazine derivatives of 3-methyl-5-spirofluorenehydantoin in search of structural features of P-gp inhibitors." Acta Crystallographica Section C Structural Chemistry 77, no. 8 (2021): 467–78. http://dx.doi.org/10.1107/s2053229621006756.

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5-Spirofluorenehydantoin derivatives show efflux modulating, cytotoxic and antiproliferative effects in sensitive and resistant mouse T-lymphoma cells. In order to extend the knowledge available about the pharmacophoric features responsible for the glycoprotein P (P-gp) inhibitory properties of arylpiperazine derivatives of 3-methyl-5-spirofluorenehydantoin, we have performed crystal structure analyses for 1-[3-(3′-methyl-2′,4′-dioxospiro[fluorene-9,5′-imidazolidin]-1′-yl)propyl]-4-phenylpiperazine-1,4-diium dichloride monohydrate, C29H32N4O2 2+·2Cl−·H2O (1), 3′-methyl-1′-{3-[4-(4-nitrophenyl)
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Sun, Na-Bo, Guo-Wu Rao, and Jian-Bo Chu. "1-{[3-(2-Chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethylcyclopropan-1-yl]carbonyl}-3-(methylsulfonyl)imidazolidin-2-one." Acta Crystallographica Section E Structure Reports Online 68, no. 6 (2012): o1744. http://dx.doi.org/10.1107/s1600536812021216.

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In the title molecule, C13H16ClF3N2O4S, the imidazolidine ring is approximately planar, the largest deviation from this plane being 0.025 (3) Å. The cyclopropane ring forms a dihedral angle of 64.1 (2)° with the imidazolidine ring. In the crystal, C—H...O hydrogen bonds are observed.
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Umar, M. Naveed, M. Nawaz Tahir, Mohammad Shoaib, Akbar Ali, and Imran Khan. "1,3-Bis(1-phenylethyl)imidazolidine-2-thione." Acta Crystallographica Section E Structure Reports Online 68, no. 4 (2012): o1188. http://dx.doi.org/10.1107/s160053681201224x.

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The complete molecule of the title compound, C19H22N2S, is generated by crystallographic twofold symmetry with the C=S group lying on the rotation axis. The imidazolidine ring adopts a flattened twist conformation. The dihedral angle between the asymmetric part of the imidazolidine-2-thione fragment and the benzene ring is 89.49 (17)°.
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Raper, Eric S., John D. Wilson та William Clegg. "[Bis{bis(imidazolidine-2-thione)-μ2-(imidazolidine-2-thione)copper(I)}] diperchlorate: synthesis and crystal structure". Inorganica Chimica Acta 194, № 1 (1992): 51–55. http://dx.doi.org/10.1016/s0020-1693(00)85822-3.

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Shtamburg, Vasiliy G., Andrey A. Anishchenko, Victor V. Shtamburg, et al. "Synthesis and crystal structure of new imidazolidine-2,4-dione and imidazolidin-2-one derivatives." Mendeleev Communications 18, no. 2 (2008): 102–4. http://dx.doi.org/10.1016/j.mencom.2008.03.018.

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Dissertations / Theses on the topic "Imidazolidine-2"

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Geittner, Florian. "2-Alkyliden-imidazolidine als „Superbasen“ für stereokontrollierte HX- und Dibrom-Eliminierungen." Diss., Ludwig-Maximilians-Universität München, 2014. http://nbn-resolving.de/urn:nbn:de:bvb:19-171030.

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Auf mehreren unterschiedlichen Synthesewegen wurden sterisch unterschiedlich anspruchsvolle, chirale 2-Alkyliden-imidazolidine hergestellt. Das sterisch anspruchvollste ist das 2-Bornyliden-imidazolidin. Sie wurden als „Superbasen“ in Bromwasserstoff-, Toluolsulfonsäure- und α,β-Dibrom-Eliminierungen eingesetzt. Das Konformerenverhältnis der gebildeten Alkene wurde untersucht. Die 2-Alkyliden-imidazolidine wurden auf ihre Eliminierungseffizienz und auf ihre sterische und chirale Selektivität getestet. Sie wurden mit achiralen Kernstuktur-analogen 2-Alkyliden-imidazolidinen verglichen.<br>Chira
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Geittner, Florian [Verfasser], and Manfred [Akademischer Betreuer] Heuschmann. "2-Alkyliden-imidazolidine als „Superbasen“ für stereokontrollierte HX- und Dibrom-Eliminierungen / Florian Geittner. Betreuer: Manfred Heuschmann." München : Universitätsbibliothek der Ludwig-Maximilians-Universität, 2014. http://d-nb.info/1053618603/34.

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Souza, Severino Araújo de. "Estudos químicos e biológicos de compostos heterocíclicos derivados dos núcleos imidazolidina-2,4-diona e 2-tioxoimidazolidina-4-ona." Universidade Federal da Paraíba, 2015. http://tede.biblioteca.ufpb.br:8080/handle/tede/9023.

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Submitted by Maike Costa (maiksebas@gmail.com) on 2017-06-27T14:51:56Z No. of bitstreams: 1 arquivototal.pdf: 8326748 bytes, checksum: beabc8048bb16f0e1b36cca198214348 (MD5)<br>Made available in DSpace on 2017-06-27T14:51:56Z (GMT). No. of bitstreams: 1 arquivototal.pdf: 8326748 bytes, checksum: beabc8048bb16f0e1b36cca198214348 (MD5) Previous issue date: 2015-04-06<br>Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES<br>The breakthrough occurred in the scientific world involving chemical and pharmacological studies of heterocyclic are the result of the large investment from
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Courvoisier, Laurent. "Polymorphisme et cristallisation préférentielle : applications aux dérivés(+-)5-méthyl-5-aryl-imidazolidine 2,4-dione et au (+-)(2-(diphénylméthyl)sulfinyl)acétamide." Rouen, 2003. http://www.theses.fr/2003ROUES020.

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Le dédoublement par cristallisation préférentielle de dérivés 5-méthyl-5-aryl-imidazolidine-2,4-dione a été réalisé selon deux procédés AS3PC (Auto-Seeded Programmed Polythermic Preferential crystallization) à une échelle de 2L et 10 L. Le suivi de l'évolution de la population de particules pendant la cristallisation permet de conclure que l'effet d'entraînement n'est pas le fait d'un mécanisme unique. L'effet du polymorphisme a été étudié sur les deux procédés. Cinq nouvelles formes polymorphiques et quatre solvates du(+ -)(2-(diphénylméthyl)sulfinyl)-N-acétamide ont été préparés et caractéri
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Benamour, Khalid. "Produits dérivés de la 2-iminoimidazolidine : synthèse, structure et résultats pharmacologiques." Université Joseph Fourier (Grenoble), 1993. http://www.theses.fr/1993GRE18013.

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Cristina, Apolinário da Silva Andréa. "Novas imidazolidinas potencialmente esquistossomicidas : bioatividade de 2-Tioxo-Imidazolidin-4- onas frente a vermes adultos de Schistosoma mansoni (CEPA BH)." Universidade Federal de Pernambuco, 2004. https://repositorio.ufpe.br/handle/123456789/1396.

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Made available in DSpace on 2014-06-12T15:49:42Z (GMT). No. of bitstreams: 2 arquivo4428_1.pdf: 1859764 bytes, checksum: f95857a109be3e58cbeb1a51410257ae (MD5) license.txt: 1748 bytes, checksum: 8a4605be74aa9ea9d79846c1fba20a33 (MD5) Previous issue date: 2004<br>Coordenação de Aperfeiçoamento de Pessoal de Nível Superior<br>Foram obtidos oito novos derivados bioisósteros das séries 5- benzilideno-3-(4-nitro-benzil)-2-tioxo-imidazolidin-4-ona 10a-d e 5-benzilideno- 3-[2-oxo-2-(4-nitro-fenil)-etil]-2-tioxo-imidazolidin-4-ona 12a-d. A síntese foi realizada a partir da 2-tioxo-imidazolidin-4-
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dos, Santos Carvalho Manuela. "Síntese, determinação estrutural citotóxica in vitro de novos compostos de coordenação de platina contendo como ligantes compostos imidazolidínicos derivados da 2-tioxo-imidazolidin-4-ona e da Imidazolidina-2,4-diona." Universidade Federal de Pernambuco, 2009. https://repositorio.ufpe.br/handle/123456789/1562.

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Made available in DSpace on 2014-06-12T15:51:10Z (GMT). No. of bitstreams: 2 arquivo1569_1.pdf: 1645034 bytes, checksum: 133b99be1981cae36ade02800e5c6a81 (MD5) license.txt: 1748 bytes, checksum: 8a4605be74aa9ea9d79846c1fba20a33 (MD5) Previous issue date: 2009<br>Coordenação de Aperfeiçoamento de Pessoal de Nível Superior<br>A cisplatina é um quimioterápico altamente potente comumente usado em muitos tipos de neoplasias humanas, porém devido a muitas limitações, há a necessidade de busca de novos agentes anticâncer menos tóxicos e mais seletivos, sendo assim, uma variedade de complexos de pla
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Boutin, Valérie. "Étude de quelques dérivés de la thio-2-hydantoïne : synthèse et résultats pharmacologiques." Université Joseph Fourier (Grenoble), 1989. http://www.theses.fr/1989GRE18009.

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Blanc, Madeleine. "Contribution à l'étude de dérivés de la thio-2- hydantoïne : synthèses et résultats pharmacologiques." Université Joseph Fourier (Grenoble), 1989. http://www.theses.fr/1989GRE18010.

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Chang-Fong, Jean. "Pharmacomodulation des dérivés de structure 2-iminoimidazolidine à visée antihypertensive." Université Joseph Fourier (Grenoble), 1999. http://www.theses.fr/1999GRE18001.

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Book chapters on the topic "Imidazolidine-2"

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Bottomley, Peter, Richard A. Hoodless, and Nigel A. Smart. "Review of Methods for the Determination of Ethylenethiourea (Imidazolidine-2-Thione) Residues." In Residue Reviews. Springer New York, 1985. http://dx.doi.org/10.1007/978-1-4612-5132-3_2.

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Wohlfarth, Ch. "Dielectric constant of 1,3-dimethyl-2-imidazolidinone." In Supplement to IV/6. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75506-7_149.

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Wohlfarth, Ch. "Dielectric constant of the mixture (1) water; (2) 1,3-dimethyl-2-imidazolidinone." In Supplement to IV/6. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75506-7_361.

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"1H-Pyrazol-2-ium to Imidazolidine." In Substance Index, edited by Backes, Fröhlich, and Pedeken. Georg Thieme Verlag, 1999. http://dx.doi.org/10.1055/b-0035-114065.

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Stanovnik, B., and J. Svete. "From 2-(Aroylmethylene)imidazolidines." In Five-Membered Hetarenes with Two Nitrogen or Phosphorus Atoms. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-012-00168.

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"Imidazolidines, Imidazolidinethiones, and 2-Imidazolidones." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186541.ch12.

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Guichard, G. "Sequential Reaction of -(2-Nitrobenzenesulfonyl)imidazolidinone." In Four Carbon-Heteroatom Bonds. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-018-00965.

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"The Imidazolines, 2-Imidazolidones, 2-Imida-Zolidinethiones, 2-Iminoimidazolidines, and Imidazolidines." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186541.ch7.

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Conference papers on the topic "Imidazolidine-2"

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Kosmas, Agnie Mylona, Demetrios K. Papayannis, Theodore E. Simos, and George Maroulis. "Computational Studies on Dihalogen Complexes of N-methyl Imidazoline-2-thione and N-methyl Imidazolidine-2-thione." In COMPUTATIONAL METHODS IN SCIENCE AND ENGINEERING: Theory and Computation: Old Problems and New Challenges. Lectures Presented at the International Conference on Computational Methods in Science and Engineering 2007 (ICCMSE 2007): VOLUME 1. AIP, 2007. http://dx.doi.org/10.1063/1.2836193.

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Saloutina, L. V., A. Ya Zapevalov, M. I. Kodess, et al. "Reactions of trifluoromethylated imidazolidin-2-ones with urea." In ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0069427.

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Smit, Biljana, Petar Stanic, and Marija Zivkovic. "Synthesis, characterization and an extensive biological evaluation of 5-​[2-​(methylthio)​ethyl]​-​3-​(2-​propen-​1-​yl)​-​2-​thioxo-4-​imidazolidinone." In 4th International Electronic Conference on Medicinal Chemistry. MDPI, 2018. http://dx.doi.org/10.3390/ecmc-4-05625.

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Saloutina, L. V., A. Ya Zapevalov, M. I. Kodess, et al. "Transformations of 4,5-bis(trifluoromethyl)imidazolidin-2-one and its N-substituted analogous in reactions with N,N-dinucleophiles." In ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0069424.

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