Relevant bibliographies by topics / 3-oxazolidine-2

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

Academic literature on the topic '3-oxazolidine-2'

Author: Grafiati
Published: 9 March 2023
Last updated: 31 July 2025

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Journal articles on the topic "3-oxazolidine-2"

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Wang, Linqiang, and Jiaxi Xu. "Salen–scandium(III) complex-catalyzed asymmetric (3 + 2) annulation of aziridines and aldehydes." Beilstein Journal of Organic Chemistry 21 (May 28, 2025): 1087–94. https://doi.org/10.3762/bjoc.21.86.

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Oxazolidine is one of the crucial structural moieties of biologically active compounds. A salen–scandium triflate complex-catalyzed asymmetric (3 + 2) annulation of dialkyl 1-sulfonylaziridine-2,2-dicarboxylates and aldehydes generated optically active functionalized oxazolidine derivatives in moderate to good yields and good to excellent enantioselectivities and high diastereoselectivities. A reasonable reaction mechanism was proposed and rationalized the experimental results.
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Tlekhusezh, Marina, Roman Makuilov, and Larisa Badovskaya. "3-Benzyl-4-(N-benzylcarbamoylmethyl)-2-(3-pyridyl)-1,3-oxazolidine." Molecules 5, no. 12 (2000): M141. http://dx.doi.org/10.3390/m141.

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Quick, Matthias P., Roland Fröhlich, Dirk Schepmann, and Bernhard Wünsch. "Asymmetric synthesis of 3-substituted tetrahydro-2-benzazepines." Organic & Biomolecular Chemistry 13, no. 26 (2015): 7265–81. http://dx.doi.org/10.1039/c5ob00731c.

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Yadav, Reena, Suryabhan Singh, Manoj Trivedi, et al. "New main-group ferrocenyldithiocarbamates and conversion to ferrocene oxazolidine-2-thione and -2-one." New Journal of Chemistry 44, no. 8 (2020): 3268–77. http://dx.doi.org/10.1039/c9nj06139h.

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Takibayeva, A. T., M. K. Ibraev, and S. K. Kabieva. "Synthesis of new 3-substituted 1,3-oxazolidine-2-thiones." Russian Journal of General Chemistry 87, no. 6 (2017): 1310–12. http://dx.doi.org/10.1134/s1070363217060299.

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Gao, Xing, Dongyu Zhu, Feng Jiang, et al. "Palladium-catalyzed stereoselective (3 + 2) cycloaddition of vinylethylene carbonates with cyclic N-sulfonyl ketimines." Organic & Biomolecular Chemistry 19, no. 22 (2021): 4877–81. http://dx.doi.org/10.1039/d1ob00614b.

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Fu, Ying, Yin-Xia He, Hong-Xia Hou та ін. "2,2′-Anhydro-1-(3′,5′-di-O-acetyl-β-D-arabinofuranosyl)uracil, a cyclouridine nucleoside with a C4′-endofuranosyl conformation". Acta Crystallographica Section C Crystal Structure Communications 69, № 3 (2013): 282–84. http://dx.doi.org/10.1107/s0108270113000395.

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2,2′-Anhydro-1-(3′,5′-di-O-acetyl-β-D-arabinofuranosyl)uracil, C13H14N2O7, was obtained by refluxing 2′,3′-O-(methoxymethylene)uridine in acetic anhydride. The structure exhibits a nearly perfect C4′-endo(4E) conformation. The best four-atom plane of the five-membered furanose ring is O—C—C—C, involving the C atoms of the fused five-membered oxazolidine ring, and the torsion angle is only −0.4 (2)°. The oxazolidine ring is essentially coplanar with the six-membered uracil ring [r.m.s. deviation = 0.012 (5) Å and dihedral angle = −3.2 (3)°]. The conformation at the exocyclic C—C bond isgauche–t
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Farzaliev, Vagif Majid, Malahat Talat Abbasova, Oruc Garib Nabiev, Nabat Allahverdi Alieva, Leyla Ramiz Safarova, and Garatel Maharram Kulieva. "Synthesis and study of a disinfectant based on diethanolamine." Disinfection affairs, no. 1 (March 2023): 56–62. http://dx.doi.org/10.35411/2076-457x-2023-1-56-62.

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The interaction of diethanolamine with formaldehyde at a ratio of initial reagents of 2?:?3, respectively, obtained a preparation that is an equimolar mixture of 3-(?-hydroxyethyl)-1,3-oxazolidine and its methylol derivative – 3-(?-hydroxyoxymethyl-ethyl)-1,3-oxazolidine. The paper presents the results of a study of the antimicrobial activity of the preparation against microorganisms – S. aureus, E. coli, as the most resistant species of bacteria that cause nosocomial infection. The tests were carried out by three methods: the test object method, as well as suspension and adsorption methods. T
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Nogueira, Thais C. M., Alessandra C. Pinheiro, James L. Wardell, Marcus V. N. de Souza, Jordan P. Abberley та William T. A. Harrison. "Weak C—H...O and C—H...π hydrogen bonds and π–π stacking interactions in a series of fourN′-[(E)-(aryl)methylidene]-N-methyl-2-oxo-1,3-oxazolidine-4-carbohydrazides". Acta Crystallographica Section C Structural Chemistry 71, № 8 (2015): 647–52. http://dx.doi.org/10.1107/s2053229615012450.

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Oxazolidin-2-ones are widely used as protective groups for 1,2-amino alcohols and chiral derivatives are employed as chiral auxiliaries. The crystal structures of four differently substituted oxazolidinecarbohydrazides, namelyN′-[(E)-benzylidene]-N-methyl-2-oxo-1,3-oxazolidine-4-carbohydrazide, C12H12N3O3, (I),N′-[(E)-2-chlorobenzylidene]-N-methyl-2-oxo-1,3-oxazolidine-4-carbohydrazide, C12H12ClN3O3, (II), (4S)-N′-[(E)-4-chlorobenzylidene]-N-methyl-2-oxo-1,3-oxazolidine-4-carbohydrazide, C12H12ClN3O3, (III), and (4S)-N′-[(E)-2,6-dichlorobenzylidene]-N,3-dimethyl-2-oxo-1,3-oxazolidine-4-carbohy
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T, Panneer Selvam, Ramu P., and Siva Kumar A. "Synthesis, Characterization and Biological Activity of novel 3-benzyl-2- (4'-substituted phenyl)-4(5H)-(4''-nitrophenyl amino)-1, 3-oxazolidines." International Journal of Drug Design and Discovery 2, no. 1 (2024): 369–74. https://doi.org/10.37285/ijddd.2.1.3.

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Here, we describe the design, synthesis, and biological evaluation of oxazolidine derivatives. Oxazolidine ring is a reduced form of oxazole system; many of its derivatives possess interesting biological activities, such as anti-convulsant, anti-microbial, analgesic, anti-inflammatory and anti-tumor. In our study, the biological activity of synthesized novel 3-benzyl-2-(4'-substituted phenyl)-4(5H)-(4''-nitrophenyl amino)-1, 3-oxazolidines 6a-e were characterized by antimicrobial screening against several gram-positive, gram negative bacteria and fungus. The purity of the synthesized compounds
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Dissertations / Theses on the topic "3-oxazolidine-2"

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Tardy, Sébastien. "Méthodologie de N-vinylation de spiro-1,3-oxazolidine-2-thiones sur charpentes saccharidiques et évaluation en hétérocycloaddition de Diels-Alder [4+2] à demande inverse." Phd thesis, Université d'Orléans, 2007. http://tel.archives-ouvertes.fr/tel-00152838.

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Les 1,3-oxazolidinethione-2-thiones (OZT), fonctions thionocarbamates cycliques, ancrées sur des charpentes saccharidiques font l'objet de notre étude. Les travaux menés ont été axés vers l'emploi des OZT chirales en synthèse asymétrique. Dans ce but, nous avons développé une méthodologie de synthèse d'OZT spiraniques sur charpentes saccharidiques ainsi qu'une méthode de N-vinylation des OZT, en poursuivant les connaissances acquises au sein du laboratoire. La chiralité inhérente aux sucres, couplée à la réactivité toute particulière des OZT obtenues, nous a permis d'explorer la réactivité d'a
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Huang, Chih-Wei, and 黃智偉. "A study of the effect of 3-butyl-2-1-ethylpentyl-oxazolidine as drying agent for moisture-curable polyurethane." Thesis, 2007. http://ndltd.ncl.edu.tw/handle/jdch9g.

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碩士<br>國立臺灣科技大學<br>高分子系<br>95<br>A study of the PU system of MDI and PPG, with DMDEE as catalyst and 3-butyl-2-1-ethylpentyl-oxazolidine as drying agent, was presented to observe the reacting rate and physical properties of wet-curing process. The drying agent, 3-butyl-2-1-ethylpentyl-oxazolidine, can reduce the variation of viscosity effectually and didn’t induce the cytotoxicity and suits for the application of medical material as well. With the increasing of molar ratio of MDI, the reaction rate and mechanical properties was increasing and the temperature of glass transition was elev
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Book chapters on the topic "3-oxazolidine-2"

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O'Grady, Ella, Greta Pileckaite, Almha Gilheany, Endrita Kucana, Swarna Jaiswal, and Amit K. Jaiswal. "Health-promoting effects of glucosinolates and their breakdown products." In Understanding and optimising the nutraceutical properties of fruit and vegetables. Burleigh Dodds Science Publishing, 2022. http://dx.doi.org/10.19103/as.2022.0101.07.

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Glucosinolates (GLs) are a large group of secondary metabolites which are found in cruciferous plants such as broccoli, cabbage, and kale and contain nutritional and physiological active properties. Several factors affect composition levels of glucosinolates such as storage conditions, methods of consuming vegetables as well as agricultural and environmental factors. When cruciferous vegetables are consumed raw, the myrosinase enzyme found in these plants hydrolyzes the GLs in the proximal gastrointestinal tract to produce a variety of metabolites such as isothiocyanates, nitriles, oxazolidine
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Taber, Douglass F. "The Nakada Synthesis of (-)-FR182877." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0084.

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The Streptomyces metabolite (-)-FR182877 3 binds to and stabilizes microtubules, showing the same potency of anticancer activity as Taxol (paclitaxel). Masahisa Nakada of Waseda University assembled (Angew. Chem. Int. Ed. 2009, 48, 2580) the hexacyclic ring system of 3 by the tandem intramolecular Diels-Alder–intramolecular hetero Diels-Alder cyclization of 1, generating seven new stereogenic centers in a single step. The construction of the pentaene substrate 1 started with the known aldehyde 4, prepared by homologation of commercial ethyl 3-methyl-4-oxocrotonate. Addition of the propionyl ox
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Conference papers on the topic "3-oxazolidine-2"

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Baraka-Lokmane, Salima, Jean-Marc Boumera, and Frédéric Faucheux. "Selection of the Appropriate H2S Scavenger Chemistry Based on the Mineral Scaling Risk." In Gas & Oil Technology Showcase and Conference. SPE, 2023. http://dx.doi.org/10.2118/214095-ms.

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Abstract The study concerns a non-conventional field in the Middle East, where gas contains 4 mol% of H2S and 3 mol% of CO2. Gas is exported and production water is reinjected in the aquifer. The first target is to have H2S level in the injected water around 400 ppm and the second target is to have H2S level in the injected water lower than 60 ppm. Quantity of water to be treated will be around 10 000 bbl/d for the first weeks and decreasing up-to few 100s bbl/d after some months. The objective of this paper is (i) the evaluation of the scaling risk; (ii) identification of suitable H2S scaveng
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Journal articles
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