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

Author: Grafiati

Published: 9 March 2023

Last updated: 31 July 2025

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1

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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2

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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3

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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4

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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5

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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6

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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7

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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8

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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9

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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10

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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11

Zou, Ye-cheng, Zhi-yong Hu, and Duan-lin Cao. "3-(4,6-Dichloro-1,3,5-triazin-2-yl)-2,2-dimethyl-1,3-oxazolidine." Acta Crystallographica Section E Structure Reports Online 68, no. 7 (2012): o2142. http://dx.doi.org/10.1107/s1600536812026578.

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12

Luk'yanov, B. S., N. B. Ivanov, L. E. Nivorozhkin, and V. I. Minkin. "5,5-Dimethyl-2-thioxo-3-phenylspiro(1,3-oxazolidine-4,2-[2H]chromenes)." Chemistry of Heterocyclic Compounds 26, no. 6 (1990): 712–13. http://dx.doi.org/10.1007/bf00756437.

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13

Pilotzi Xahuentitla, Hugo, Jesús Guadalupe Ortega Montes, Dino Hernán Gnecco Medina, Joel Luis Terán Vázquez, Emanuel Hernández Núñez, and Maria Laura Orea Flores. "Synthesis of Methyl 2-((4R)-3-Acryloyl-4-phenyloxazolidin-2-yl)acetates." Molbank 2024, no. 4 (2024): M1903. http://dx.doi.org/10.3390/m1903.

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The chiral oxazolidine moiety is an important core in asymmetric synthesis due to its ability to participate in various stereoselective chemical reactions and because it forms part of more complex and important active compounds. Therefore, in this letter we report a convenient diastereoselective and practical strategy for the synthesis of chiral methyl 2-((4R)-3-acryloyl-4-phenyloxazolidin-2-yl)acetates, starting from (R)-(–)-2-phenylglycinol and methyl propiolate, which were obtained via two simple chemical and stereoselective reactions.

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14

Kutschy, Peter, Milan Dzurilla, Ladislav Kniežo, et al. "Reactions of 3-butine-2-methyl-2-ol with isothiocyanates." Collection of Czechoslovak Chemical Communications 51, no. 5 (1986): 1119–26. http://dx.doi.org/10.1135/cccc19861119.

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3-Butine-2-methyl-2-ol reacts with isothiocyanates in the presence of sodium hydride in dimethylformamide to give various products depending on structure of the isothiocyanate residue. Isothiocyanates with the NCS group bound to sp2 carbon atom (phenyl, 4-bromophenyl, and styryl isothiocyanates) give the respective 1,3-oxazolidine derivatives. If the NCS group is bound to an sp3-hybridized carbon atom (ethyl and benzyl isothiocyanates), derivatives of 1,3-oxathiolane are formed. Acyl isothiocyanates (benzoyl and 3-phenylpropenoyl isothiocyanates) give products of substitution of the NCS group,

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15

Gass, Ian A., Mousa Asadi, David W. Lupton, et al. "Manganese(II) Oxazolidine Nitroxide Chelates: Structure, Magnetism, and Redox Properties." Australian Journal of Chemistry 67, no. 11 (2014): 1618. http://dx.doi.org/10.1071/ch14390.

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The mononuclear oxazolidine nitroxide complex [MnII(L•)2](ClO4)2 (1) (L•, 4-dimethyl-2,2-di(2-pyridyl)oxazolidine N-oxide) has been synthesized and investigated using single-crystal X-ray diffraction, variable-temperature magnetic susceptibility measurements, and electrochemistry. The structural analysis reveals bond lengths compatible with a linear L•–MnII–L• arrangement where the ligands are in the neutral ligand form and the central MnII ion is high spin (S = 5/2). Although analysis of the variable-temperature magnetic susceptibility data suggests a strong antiferromagnetic metal–radical in

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16

Wrobel, Jay, and Arlene Dietrich. "Syntheses of Spiro(oxazolidinediones): Spiro[1H-isoindole-1,5'-oxazolidine]-2',3(2H),4'-triones and Spiro[1,2-benzisothiazole-3(2H),5'-oxazolidine]-2',4'-dione 1,1-Dioxides." HETEROCYCLES 38, no. 8 (1994): 1823. http://dx.doi.org/10.3987/com-94-6750.

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17

Erdsack, Jörg, Markus Schürmann, Hans Preut, and Norbert Krause. "tert-Butyl 2,2-dimethyl-4-(3-phenyl-2,5-dihydrofuran-2-yl)oxazolidine-3-carboxylate." Acta Crystallographica Section E Structure Reports Online 63, no. 2 (2007): o664—o665. http://dx.doi.org/10.1107/s1600536807000839.

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18

Brewer, Cynthia T., Greg Brewer та Raymond J. Butcher. "Chirality Transfer and Oxazolidine Formation in Reaction of L and D Enantiomers of β-Hydroxy Amino Acids with Nitrogenous Carboxaldehydes and Nickel(II)". Molecules 30, № 14 (2025): 2913. https://doi.org/10.3390/molecules30142913.

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The reaction of either the L (2S3R) or D (2R3S) enantiomers of H2N-C*H(R)CO2− (R = -C*H(OH)CH3 or -C*H(OH)CH(CH3)2) and the L (2S) or D (2R) enantiomers of H2N-C*H(C(CH3)2OH)CO2− with imidazole-4-carboxaldehyde and nickel(II) acetate in methanol yields a single stereoisomer of an oxazolidine. There is retention of chirality on ring positions 4 and 5 (if Cβ is chiral) of the oxazolidine, Cα and Cβ of the parent amino acid, and transfer of chirality to the newly generated stereogenic centers, ring positions 3, the amino acid nitrogen atom, NAA, and 2, the aldehyde carbon atom, Cald. Specifically

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19

Rey, Philippe, Andrea Caneschi, Taisiya S. Sukhikh, and Kira E. Vostrikova. "Tripodal Oxazolidine-N-Oxyl Diradical Complexes of Dy3+ and Eu3+." Inorganics 9, no. 12 (2021): 91. http://dx.doi.org/10.3390/inorganics9120091.

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Two diradical complexes of the formula [LnRad2(CF3SO3)3] c (Ln(III) = Dy, Eu, Rad = 4,4-dimethyl-2,2-bis(pyridin-2-yl)-1,3-oxazolidine-3-oxyl) were obtained in air conditions. These are the first examples of diradical compounds of lanthanides and oxazolidine nitroxide. The complexes were characterized crystallographically and magnetically. Single crystal XRD analysis revealed that their coordination sphere is composed of three monodentate triflates and two tripodal Rad, which coordinate the central atom in a tridentate manner via two N atoms of the pyridine groups and the O atom of a nitroxide

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20

Aumann, Rudolf, Eberhard Kuckert, and Heinrich Heinen. "3-Aminoindole, Imidazolidine und Oxazolidine aus Isocyaniden und Carbenkomplexen durch metallinduzierte [4+2]- bzw. [3+2]-Cycloadditionen." Angewandte Chemie 97, no. 11 (1985): 960–62. http://dx.doi.org/10.1002/ange.19850971109.

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21

Hardgrove Jnr, G. L., J. S. Clark, R. M. Hanson, and A. Q. Thieu. "Structure of (S,S)-(E)-3-(2-butenoyl)-2,4-bis(phenylmethyl)oxazolidine." Acta Crystallographica Section C Crystal Structure Communications 49, no. 2 (1993): 336–38. http://dx.doi.org/10.1107/s0108270192004761.

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22

Quinsac, Alain, Daniel Ribaillier, Patrick Rollin, and Michel Dreux. "Analysis of 5-Vinyl-l,3-Oxazolidine-2-Thione by Liquid Chromatography." Journal of AOAC INTERNATIONAL 75, no. 3 (1992): 529–36. http://dx.doi.org/10.1093/jaoac/75.3.529.

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Abstract 5-Vlnyl-1,3-oxazolldlne-2-thlone (5-VOT) Is a goltrlgenlc compound released by enzymatic degradation of progoltrln, the major glucoslnolate occurring In rapeseed meal. A liquid chromatographic (LC) method for determination of 5-VOT in a biological environment Is presented. Complete extraction of 5-VOT has been carried out by complexatlon with phenyl mercury acetate under cyclohexanlc conditions, and then by decomplexation using an aqueous sodium thlosulfate solution. These reactions displace 5-VOT from an aqueous to an organic medium, and then back again to the aqueous condition, thus

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23

Weigand, Wolfgang, Ulrich Nagel, and Wolfgang Beck. "Pseudohalogeno-Metallverbindungen, LXVIII [1]. Reaktionen der Cyanometallsäuren NCAuCNH, (NC)4Pt(CNH)2, (NC)2M(CNH)4(M = Fe, Ru, Os) und Co[bis(dimethyIglyoximato)](CN)CNHmit Epoxiden: 2-Hydroxyalkylisocyanid- und Oxazolidin-2-yIiden-MetalIkomplexe / Pseudohalogeno Metal Compounds, LXVIII [1]. Reaction of Cyano Metal Acids NCAuCNH, (NC)4Pt(CNH)2, (NC)2M(CNH)4 (M = Fe, Ru, Os) and Co[bis(dimethylglyoximato)](CN)CNH with Epoxides: 2-Hydroxyalkylisocyanide and Oxazolidine-2-ylidene Metal Complexes." Zeitschrift für Naturforschung B 43, no. 3 (1988): 328–38. http://dx.doi.org/10.1515/znb-1988-0316.

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NCAuCNH reacts with expoxides to give oxazolidine-2-ylidene (2) and 2-hydroxyalkyl complexes (3), respectively. Complexes with cyclic carbene ligands [XXX] (5) and [XXX] (7) are formed from the corresponding isocyanic metal compounds and oxiranes. 5b has been characterized by crystal structure determination. Ring opening of phenyloxirane occurs at the phenyl substituted carbon atom. (NC)2M(CNH)4 (M = Fe, Ru, Os) and oxirane yield mixtures of [XXX] and [XXX].

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24

Bolte, M., and S. Monz. "4-Ethyl-2-[4-hydroxy-5-(1-hydroxypropyl)-2-phenyl-2-cyclohexenyl]-3-tosyl-1,3-oxazolidine." Acta Crystallographica Section C Crystal Structure Communications 53, no. 10 (1997): IUC9700014. http://dx.doi.org/10.1107/s0108270197099411.

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25

Rey, Philippe, Anton I. Smolentsev, and Kira E. Vostrikova. "Oxazolidine Nitroxide Transformation in a Coordination Sphere of the Ln3+ Ions." Molecules 27, no. 5 (2022): 1626. http://dx.doi.org/10.3390/molecules27051626.

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Upon the interaction of the hydrated lanthanide(III) salts found in acetonitrile solution with a tripodal paramagnetic compound, 4,4-dimethyl-2,2-bis(pyridin-2-yl)-1,3-oxazolidine-3-oxyl (Rad), functionalized by two pyridyl groups, three neutral, structurally characterized complexes with diamagnetic polydentate ligands—[Dy(RadH)(hbpm)Cl2], [Yb2(ipapm)2(NO3)4], and [Ce2(ipapm)2(NO3)4(EtOAc)2]—were obtained. These coordination compounds are minor uncolored crystalline products, which were formed in a reaction mixture due to the Rad transformation in a lanthanide coordination sphere, wherein the

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26

WROBEL, J., and A. DIETRICH. "ChemInform Abstract: Syntheses of Spiro(oxazolidinediones): Spiro(1H-isoindole-1,5′- oxazolidine)-2′,3(2H),4′-triones and Spiro(1,2-benzisothiazole-3(2H),5′ -oxazolidine)-2′,4′-dione 1,1-Dioxides." ChemInform 25, no. 46 (2010): no. http://dx.doi.org/10.1002/chin.199446147.

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27

Dettwiler, James E., Laurent Bélec та William D. Lubell. "Synthesis and application of L-N-Boc-N-methyl-β-hydroxyvaline in the preparation of a depsipeptide". Canadian Journal of Chemistry 83, № 6-7 (2005): 793–800. http://dx.doi.org/10.1139/v05-033.

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Enantiopure (>99% ee) L-N-tert-butyloxycarbonyl-N-methyl-β-hydroxyvaline (2) was synthesized in six steps and 43% overall yield from D-serine methyl ester (5). Methyl (4S)-N-(9-phenylfluoren-9-yl)-oxazolidine-4-carboxylate (7) was prepared in two steps and 73% yield by N-phenylfluorenation of 5 followed by cyclization of N-(PhF)amino alcohol 6 with formaldehyde and catalytic p-toluenesulfonic acid (PhF = 9-phenylfluoren-9-yl). The addition of MeLi to oxazolidine carboxylate 7 produced the tertiary alcohol 8 in 91% yield. Oxazolidines 8 equilibrated with oxazolidine 9 under acidic conditions

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28

Makaev, F. Z., F. G. Shepel, S. T. Malinovskii, and M. Gdaniec. "Effective synthesis and X-ray investigation of (±)-2S-2-(2-chlorophenyl)-3-acetyl-1,3-oxazolidine." Journal of Structural Chemistry 46, no. 6 (2005): 1118–21. http://dx.doi.org/10.1007/s10947-006-0254-3.

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29

LUK'YANOV, B. S., N. B. IVANOV, L. E. NIVOROZHKIN, and V. I. MINKIN. "ChemInform Abstract: 5,5-Dimethyl-2-thioxo-3-phenylspiro(1,3-oxazolidine-4,2-(2H)chromenes)." ChemInform 22, no. 11 (2010): no. http://dx.doi.org/10.1002/chin.199111182.

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30

Berredjem, Malika, Assia Allaoui, Amani Direm, Noureddine Aouf, and Nourredine Benali-Cherif. "(4S)-4-Benzyl-N-{[(4S)-4-benzyl-2-oxo-1,3-oxazolidin-3-yl]sulfonyl}-2-oxo-1,3-oxazolidine-3-carboxamide." Acta Crystallographica Section E Structure Reports Online 66, no. 7 (2010): o1611—o1612. http://dx.doi.org/10.1107/s1600536810020866.

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31

Saito, Katsuhiro, Hiroyuki Watanabe, Michihito Sakura, and Kensuke Takahashi. "[2+3]-Type Addition Reactions of Benzocyclobutadiene with Nitrone Derivatives. Formation of Oxazolidine Derivatives." Bulletin of the Chemical Society of Japan 66, no. 3 (1993): 981–83. http://dx.doi.org/10.1246/bcsj.66.981.

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32

Eggleston, D. S., A. Abdel-Magid, L. N. Pridgen, and I. Lantos. "Structures of three stereoisomers of (4S)-3-(2-chloro-3-hydroxy-4-methylpentanoyl)-4-(1-methylethyl)oxazolidine." Acta Crystallographica Section C Crystal Structure Communications 42, no. 10 (1986): 1416–20. http://dx.doi.org/10.1107/s0108270186092065.

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33

Husain, Syed Masood, Roland Fröhlich, Dirk Schepmann, and Bernhard Wünsch. "Enantioselective Synthesis of a 2,2-Disubstituted Tetrahydro-3- benzazepine as Novel NMDA Receptor Antagonist." Zeitschrift für Naturforschung B 65, no. 2 (2010): 191–96. http://dx.doi.org/10.1515/znb-2010-0216.

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The tricyclic oxazolidines trans-4 and cis-4 were interconverted upon treatment with allyltrimethylsilane/ TiCl4. The oxazolidine trans-4 was diastereoselectively reacted with PhMgBr to yield the 4,4-disubstituted 3-benzazepinone 6, along with two side products. An X-ray crystal structure analysis of 6 proved the (R)-configuration of the stereogenic center C-4 and thus the retention of configuration. Reduction of 6 with AlCl3/LiAlH4 (1/3) followed by hydrogenolysis with H2, Pd/C resulted in the formation of enantiomerically pure 2-methyl-2-phenyl-tetrahydro-3-benzazepine 11 which has a moderat

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34

Montiel-Smith, Sara, Sylvain Bernès, Jesús Sandoval-Ramírez, Socorro Meza-Reyes, and Joëlle Dubois. "3-tert-Butyl 5-methyl (2R,4S,5R)-2-(4-methoxyphenyl)-4-(3-nitrophenyl)-1,3-oxazolidine-3,5-dicarboxylate." Acta Crystallographica Section E Structure Reports Online 68, no. 11 (2012): o3146—o3147. http://dx.doi.org/10.1107/s160053681204192x.

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35

Dobkowski, J., R. Kołos, and J. Waluk. "Spectroscopy and Photophysics of 3'-[p-(dimethylamino)phenyl]spiro-[fluorene-9,4'-oxazolidine]-2',5'-dione." Acta Physica Polonica A 88, no. 3 (1995): 445–54. http://dx.doi.org/10.12693/aphyspola.88.445.

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36

Gao, Jun, Ping Zhang, and Jingxin Lei. "Synthesis of 2-phenyl-3-hydroxyethanyl-1,3-oxazolidine and its application as latent curing agents." Journal of Applied Polymer Science 106, no. 2 (2007): 1343–46. http://dx.doi.org/10.1002/app.26582.

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37

Garcia Fernandez, Jose M., Carmen Ortiz Mellet, Jose L. Jimenez Blanco, and Jose Fuentes. "Enantiopure 2-Thioxotetrahydro-1,3-O,N-heterocycles from Carbohydrates. 3. Enantiopure C-4 Chiral Oxazine- and Oxazolidine-2-thiones from 3-Deoxy-3-isothiocyanato Sugars." Journal of Organic Chemistry 59, no. 19 (1994): 5565–72. http://dx.doi.org/10.1021/jo00098a014.

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38

Hoppe, Inga, Dieter Hoppe, Regine Herbst-Irmer, and Ernst Egert. "Asymmetric aldol addition reactions of a chiral 3-sulfonyl-1,3-oxazolidine-masked lithium 2-formylcyclohexanone enolate." Tetrahedron Letters 31, no. 47 (1990): 6859–62. http://dx.doi.org/10.1016/s0040-4039(00)97190-9.

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39

Luk'yanov, B. S., L. E. Nivorozhkin, Yu E. Chernysh, and V. I. Minkin. "Photo- and thermochromic spirans. 16. 2-Oxo-3-phenyl-5,5-dimethylspiro(1,3-oxazolidine-4,2?-[2h]chromenes)." Chemistry of Heterocyclic Compounds 21, no. 8 (1985): 857–61. http://dx.doi.org/10.1007/bf00519808.

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Luk'yanov, B. S., N. B. Ivanov, L. E. Nivorozhkin, V. I. Minkin, and G. S. Borodkin. "Photochromic and thermochromic spiranes. 19. 2-thioxo-3-phenyl-5,5-diivietiiylspiro (1,3-oxazolidine-4,2?-[2h]chromenes)." Chemistry of Heterocyclic Compounds 31, no. 9 (1995): 1096–102. http://dx.doi.org/10.1007/bf01165056.

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SAITO, K., H. WATANABE, M. SAKURA, and K. TAKAHASHI. "ChemInform Abstract: (2 + 3)-Type Addition Reactions of Benzocyclobutadiene with Nitrone Derivatives. Formation of Oxazolidine Derivatives." ChemInform 24, no. 28 (2010): no. http://dx.doi.org/10.1002/chin.199328194.

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Tatarov, Eugen, Clemens Bruhn, and Herbert Frauenrath. "Crystal structure of (2R*,4S*)-methyl 2-isopropyl-4-methyl-3-(2-(trimethylsilyl) ethylsulfonyl)-1,3-oxazolidine-4-carboxylate, C14H29NO5SSi." Zeitschrift für Kristallographie - New Crystal Structures 222, no. 2 (2007): 141–42. http://dx.doi.org/10.1524/ncrs.2007.0057.

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Peng, Sheng, Feng-Ling Qing, and Chang-Ming Hu. "tert-Butyl (S)-2,2-dimethyl-4-(Z-2′, 3′, 3′, 3′-tetrafluoro-1′-propenyl) oxazolidine-3-carboxylate: preparation and its nucleophilic reactions with alcohols." Journal of Fluorine Chemistry 88, no. 1 (1998): 1–2. http://dx.doi.org/10.1016/s0022-1139(97)00129-2.

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Rochon, F. D., and L. Breau. "(2S*,4S*,5R*)-4-Methyl-2-[(5S*)-3-methyl-4,5-dihydroisoxazol-5-yl]-5-phenyl-3-(toluene-4-sulfonyl)oxazolidine." Acta Crystallographica Section C Crystal Structure Communications 55, no. 8 (1999): 1373–75. http://dx.doi.org/10.1107/s0108270199005557.

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Pandey, Ashok Kumar, and Prabal Banerjee. "One-Pot Synthesis of Oxazolidine Derivatives by [3+2]-Annulation Reactions of 1-Tosyl-2-phenyl/alkylaziridines with Aryl Epoxides." Asian Journal of Organic Chemistry 5, no. 3 (2016): 360–66. http://dx.doi.org/10.1002/ajoc.201500438.

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Chrzanowska, Maria, Zofia Meissner, Joanna M. Chrzanowska, and Andrzej K. Gzella. "Synthesis and Crystal Structure of (4S)-4-Benzyl-3-(4,5-dimethoxy-2-methylbenzoyl)-2,2-dimethyl-1,3-oxazolidine." HETEROCYCLES 90, no. 1 (2015): 730. http://dx.doi.org/10.3987/com-14-s(k)54.

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Chen, Guofei, Chunling Fu, and Shengming Ma. "A novel synthesis of oxazolidine-2,4-diones via an efficient fixation of CO2with 3-aryl-2-alkynamides." Org. Biomol. Chem. 9, no. 1 (2011): 105–10. http://dx.doi.org/10.1039/c0ob00550a.

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Maezaki, Naoyoshi, Akemi Furusawa, Shuji Uchida, and Tetsuaki Tanaka. "3-Acyl-2-(N-cyanoimino)oxazolidine derivative, a new asymmetric acylating agent for racemic secondary alkyl amines." Tetrahedron 57, no. 45 (2001): 9309–15. http://dx.doi.org/10.1016/s0040-4020(01)00933-4.

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GARCIA FERNANDEZ, J. M., C. ORTIZ MELLET, J. L. JIMENEZ BLANCO, and J. FUENTES. "ChemInform Abstract: Enantiopure 2-Thioxotetrahydro-1,3-O,N-heterocycles from Carbohydrates. Part 3. Enantiopure C-4 Chiral Oxazine- and Oxazolidine-2-thiones from 3-Deoxy-3-isothiocyanato Sugars." ChemInform 26, no. 14 (2010): no. http://dx.doi.org/10.1002/chin.199514244.

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Kohno, Hitoshi, Kenji Hirai, Masahiro Hori, Yukiharu Sato, Peter Böger, and Ko Wakabayashi. "New Peroxidizing Herbicides: Activity Compared with X-Ray Structure." Zeitschrift für Naturforschung C 48, no. 3-4 (1993): 334–38. http://dx.doi.org/10.1515/znc-1993-3-435.

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Abstract:

The crystal structure of 3-(4-chloro-5-cyclopentyloxy-2-fluorophenyl)-5-isopropylideneoxazolidine- 2,4-dione (BW -4), chlorophthalim and oxyfluorfen were determined by X -ray analysis. The molecular size of these compounds was almost the same, but the angle between the oxazolidine and the phenyl ring (BW -4), the imide and phenyl ring (chlorophthalim ) and between the two phenyl rings (oxyfluorfen) differed. The phytotoxic activities, determined by growth inhibition of Scenedesmus cells, loss of chlorophyll, and peroxidative destruction of photosynthetic pigments, were different among these co

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