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Published: 9 March 2023

Last updated: 10 March 2023

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1

Tlekhusezh, Marina, Roman Makuilov, and Larisa Badovskaya. "3-Benzyl-4-(N-benzylcarbamoylmethyl)-2-(3-pyridyl)-1,3-oxazolidine." Molecules 5, no. 12 (February 23, 2000): M141. http://dx.doi.org/10.3390/m141.

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2

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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3

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 (June 2017): 1310–12. http://dx.doi.org/10.1134/s1070363217060299.

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4

Yadav, Reena, Suryabhan Singh, Manoj Trivedi, Gabriele Kociok-Köhn, Nigam P. Rath, Randolf D. Köhn, Mohd Muddassir, and Abhinav Kumar. "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

Gao, Xing, Dongyu Zhu, Feng Jiang, Jianning Liao, Wei Wang, Yongjun Wu, Lufei Zheng, and Hongchao Guo. "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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6

Fu, Ying, Yin-Xia He, Hong-Xia Hou, Wen-Bo Zhu, Hu-Lin Li, Chao Wu, and Fang-Yan Xian. "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, no. 3 (February 12, 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–transwhich is stabilized by various C—H...π and C—O...π interactions.

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7

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 (June 20, 2012): o2142. http://dx.doi.org/10.1107/s1600536812026578.

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8

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 (June 1990): 712–13. http://dx.doi.org/10.1007/bf00756437.

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9

Nogueira, Thais C. M., Alessandra C. Pinheiro, James L. Wardell, Marcus V. N. de Souza, Jordan P. Abberley, and 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, no. 8 (July 7, 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-carbohydrazide, C13H13Cl2N3O3, (IV), show that an unexpected mild-condition racemization from the chiral starting materials has occurred in (I) and (II). In the extended structures, the centrosymmetric phases, which each crystallize with two molecules (AandB) in the asymmetric unit, formA+Bdimers linked by pairs of N—H...O hydrogen bonds, albeit with different O-atom acceptors. One dimer is composed of one molecule with anSconfiguration for its stereogenic centre and the other with anRconfiguration, and possesses approximate local inversion symmetry. The other dimer consists of eitherR,RorS,Spairs and possesses approximate local twofold symmetry. In the chiral structure, N—H...O hydrogen bonds link the molecules intoC(5) chains, with adjacent molecules related by a 21screw axis. A wide variety of weak interactions, including C—H...O, C—H...Cl, C—H...π and π–π stacking interactions, occur in these structures, but there is little conformity between them.

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10

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 (January 12, 2007): o664—o665. http://dx.doi.org/10.1107/s1600536807000839.

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11

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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12

Kutschy, Peter, Milan Dzurilla, Ladislav Kniežo, Juraj Bernát, Ján Imrich, Pavol Kristian, and Róbert Nádaskay. "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, viz. 1-butine-3-methyl-3-yl benzoate and 3-phenylpropenoic anhydride.

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13

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 (November 1985): 960–62. http://dx.doi.org/10.1002/ange.19850971109.

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14

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 (February 15, 1993): 336–38. http://dx.doi.org/10.1107/s0108270192004761.

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15

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 (May 1, 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 assuring high selectivity of the extraction. Precise quantitation of 5-VOT Is completed in 10 mln by reversed-phase liquid chromatography using an isocratic elutlon with UV detection and a specially made synthetic Internal standard. Concentration steps by solid-phase chromatography and evaporation can be introduced In the analytic procedure to lower the detection limit of 5-VOT in the sample used from 100 to 0.5 ppb. Using sow milk samples, the method was tested by small measured additions of 5-VOT. The recovery rate of the product was very good (>97%). Different phases used to achieve a sensitive, rapid, and precise method are described.

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16

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 (October 15, 1997): IUC9700014. http://dx.doi.org/10.1107/s0108270197099411.

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17

Gass, Ian A., Mousa Asadi, David W. Lupton, Boujemaa Moubaraki, Alan M. Bond, Si-Xuan Guo, and Keith S. Murray. "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 interaction, the radical–radical intramolecular interaction could not be determined unambiguously from such fits. The resultant isolated S = 3/2 ground state is confirmed by low-temperature magnetization versus field measurements. Electrochemical studies reveal similar square schemes and redox intermediates to the previously reported analogues [FeII(L•)2][BF4]2 and [CoII(L•)2][NO3]2.

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18

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 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199446147.

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19

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 (November 2005): 1118–21. http://dx.doi.org/10.1007/s10947-006-0254-3.

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20

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 (December 20, 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 group. The LnO5N4 polyhedron represents a spherical capped square antiprism with point symmetry close to C4v. The data of static magnetic measurements are compatible with the presence of two paramagnetic ligands in the coordination sphere of the metal.

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21

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 (March 1, 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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22

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 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199111182.

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23

Rey, Philippe, Anton I. Smolentsev, and Kira E. Vostrikova. "Oxazolidine Nitroxide Transformation in a Coordination Sphere of the Ln3+ Ions." Molecules 27, no. 5 (March 1, 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 processes of its simultaneous disproportionation, hydrolysis, and condensation proceed differently than in the absence of Ln ions. The latter fact was confirmed by the formation of the structurally characterized product of the oxazolidine nitroxide transformation during its crystallization in toluene solution. Such a conversion in the presence of 4f elements ions is unique since no similar phenomenon was observed during the synthesis of the 3d-metal complexes with Rad.

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24

Dettwiler, James E., Laurent Bélec, and 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, no. 6-7 (June 1, 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. Reduction of pure 8 or the mixture of oxazolidines 8 and 9 with NaCNBH3 and hydrochloric acid in anhydrous dioxane afforded N-methyl amino diol 11 in 86%92% yields. Attempts to selectively oxidize N-(PhF)amino diol 11 were unsuccessful; however, hydrogenation of 11 in the presence of di-tert-butyl dicarbonate gave the corresponding N-(Boc)amino diol 12 in 82% yield. Selective oxidation of diol 12 was performed using a cocktail containing TEMPO free radical, NaClO2, and NaOCl to give L-N-Boc-N-methyl-β-hydroxyvaline (2) in 87% yield. Coupling of β-hydroxyvaline 2 and (S)-2-hydroxy-3-methylbutanoate (15) was accomplished by using the methodology of Mitsunobu to provide depsipeptide Boc-(S)-HOMeVal-(R)-Hmb (4) for use as a building block in the synthesis of the cyclic antifungal depsipeptide aureobasidin B.Key words: N-methylated amino acid, serine, depsipeptide, aureobasidin.

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25

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 (June 9, 2010): o1611—o1612. http://dx.doi.org/10.1107/s1600536810020866.

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26

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 (October 15, 1986): 1416–20. http://dx.doi.org/10.1107/s0108270186092065.

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27

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 (March 1993): 981–83. http://dx.doi.org/10.1246/bcsj.66.981.

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28

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 (October 20, 2012): o3146—o3147. http://dx.doi.org/10.1107/s160053681204192x.

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29

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 (February 1, 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 moderate affinity (Ki = 496 nM) to the PCP binding site of the NMDA receptor.

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30

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 (September 1995): 445–54. http://dx.doi.org/10.12693/aphyspola.88.445.

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31

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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32

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 (September 1994): 5565–72. http://dx.doi.org/10.1021/jo00098a014.

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33

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 (June 2007): 141–42. http://dx.doi.org/10.1524/ncrs.2007.0057.

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34

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 (January 1990): 6859–62. http://dx.doi.org/10.1016/s0040-4039(00)97190-9.

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35

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 (August 1985): 857–61. http://dx.doi.org/10.1007/bf00519808.

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36

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 (September 1995): 1096–102. http://dx.doi.org/10.1007/bf01165056.

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37

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 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199328194.

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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 (February 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 (August 15, 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 (January 11, 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 (November 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 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199514244.

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M. S嗟lhuber, M溶ica, J. Carlos Men始dez, and Carmen Avenda撲. "Synthesis of (±)-(2R*,11bS*)-3'-Aryl-9,10-dimethoxy-1,3,4,5,7,11b-hexahydrospiro[benzo[a]quinolizin-2,5'-oxazolidine]-2',4'-diones." HETEROCYCLES 29, no. 3 (1989): 477. http://dx.doi.org/10.3987/com-89-4787.

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Faucher, Nicolas, Jean-Christophe Cintrat, Martine Nierlich, and Bernard Rousseau*. "Stereoselective synthesis of a methylene group by asymmetric reduction of 2-methoxy-4,5-diphenyl-3-tosyl-1,3-oxazolidine." Tetrahedron: Asymmetry 11, no. 19 (October 2000): 4001–7. http://dx.doi.org/10.1016/s0957-4166(00)00359-1.

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HOPPE, I., D. HOPPE, R. HERBST-IRMER, and E. EGERT. "ChemInform Abstract: Asymmetric Aldol Addition Reactions of a Chiral 3-Sulfonyl-1,3- oxazolidine-Masked Lithium 2-Formylcyclohexanone Enolate." ChemInform 23, no. 7 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199207073.

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PENG, S., F. L. QING, and C. M. HU. "ChemInform Abstract: tert-Butyl (S)-2,2-Dimethyl-4- (Z-2′,3′,3′,3′-tetrafluoro-1′-propenyl)oxazolidine-3-carboxylate (III). Preparation and Its Nucleophilic Reactions with Alcohols." ChemInform 29, no. 27 (June 21, 2010): no. http://dx.doi.org/10.1002/chin.199827146.

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Lee, Dong-Ook, Lee-Yong Khil, Tong-Shin Chang, Ho-Kyu Han, Sang-Ho Chae, Mee-Young Ahn, You-Mie Lee, et al. "Effects of KST48 [(2R,5SR)3-(2-Chloro-benzoyl) -5- (4-chlorophenoxymethyl) -2 (3,4-dichlorophenyl) oxazolidine] on Glucose Transport in L6 Myocytes." Arzneimittelforschung 54, no. 12 (December 24, 2011): 835–41. http://dx.doi.org/10.1055/s-0031-1297038.

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Zarghi, A., H. Arefi, O. G. Dadrass, and S. Torabi. "Design and synthesis of new 2-aryl, 3-benzyl-(1,3-oxazolidine or 1,3-thiazolidine)-4-ones as selective cyclooxygenase (COX-2) inhibitors." Medicinal Chemistry Research 19, no. 8 (July 25, 2009): 782–93. http://dx.doi.org/10.1007/s00044-009-9230-8.

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