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Journal articles on the topic 'Oxazolidin-2-ones'

Author: Grafiati

Published: 4 June 2021

Last updated: 16 February 2022

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1

Feroci, Marta, Achille Inesi, Vittoria Mucciante, and Leucio Rossi. "New synthesis of oxazolidin-2-ones." Tetrahedron Letters 40, no. 33 (1999): 6059–60. http://dx.doi.org/10.1016/s0040-4039(99)01256-3.

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2

Tomasini, Claudia, Gaetano Angelici, and Nicola Castellucci. "Foldamers Based on Oxazolidin-2-ones." European Journal of Organic Chemistry 2011, no. 20-21 (2011): 3648–69. http://dx.doi.org/10.1002/ejoc.201100493.

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3

Tam, Tim F., Everton Thomas, and Allen Krantz. "Synthesis of 5-alkynylidene-oxazolidin-2-ones." Tetrahedron Letters 28, no. 11 (1987): 1127–30. http://dx.doi.org/10.1016/s0040-4039(00)95306-1.

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4

Chudinov, Yu B., S. B. Gashev, Yu A. Strelenko, Z. A. Starikova, M. Yu Antipin, and V. V. Semenov. "Structural features of diastereomeric oxazolidin-2-ones." Russian Chemical Bulletin 56, no. 1 (2007): 140–47. http://dx.doi.org/10.1007/s11172-007-0023-2.

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5

Luppi, Gianluigi, Chiara Soffrè, and Claudia Tomasini. "Stabilizing effects in oxazolidin-2-ones-containing pseudopeptides." Tetrahedron: Asymmetry 15, no. 10 (2004): 1645–50. http://dx.doi.org/10.1016/j.tetasy.2004.03.033.

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6

Al Shaye, Najla, and Jason Eames. "Resolution of pentafluorophenyl esters using oxazolidin-2-ones." Tetrahedron Letters 51, no. 45 (2010): 5892–95. http://dx.doi.org/10.1016/j.tetlet.2010.08.109.

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7

Tomasini, Claudia, Gaetano Angelici, and Nicola Castellucci. "ChemInform Abstract: Foldamers Based on Oxazolidin-2-ones." ChemInform 42, no. 47 (2011): no. http://dx.doi.org/10.1002/chin.201147252.

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8

Feroci, Marta, Achille Inesi, Vittoria Mucciante, and Leucio Rossi. "ChemInform Abstract: New Synthesis of Oxazolidin-2-ones." ChemInform 30, no. 45 (2010): no. http://dx.doi.org/10.1002/chin.199945139.

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9

Kurz, Thomas, and Khalid Widyan. "Synthesis of Novel 4-Functionalised Oxazolidin-2-ones." Synthesis, no. 8 (2005): 1340–44. http://dx.doi.org/10.1055/s-2005-865292.

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10

Kovalyuk, Elena, Anastasiya Vasyutina, and Vladimir Matofonov. "STUDY OF OXAZOLIDIN-2-ONES AS INHIBITORS ACID CORROSION OF STEEL." Bulletin of the Angarsk State Technical University 1, no. 14 (2020): 46–51. http://dx.doi.org/10.36629/2686-777x-2020-1-14-46-51.

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The article presents the results of a study of individual representatives of oxazolidin-2-ones as inhibitors of acid corrosion of steel. The influence of temperature and inhibitor concentration on the degree of protection was evaluated by a complete two-factor experiment. The results of electrochemical tests of steel are presented. Oxazolidin-2-ones can be attributed to a group of promising inhibitors of acid corrosion of steel and continue research.

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11

Zlotin, Sergei G., Svetlana S. Arabadzhi, Mikhail N. Zharkov та Ilya V. Kuchurov. "Synthesis of Chiral N-Nitro-oxazolidin-2-ones and O-(β-Nitraminoalkyl) Carbamates in Liquefied 1,1,1,2-Tetrafluoroethane Medium". Synthesis 52, № 22 (2020): 3485–91. http://dx.doi.org/10.1055/s-0040-1706762.

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AbstractA convenient synthesis of chiral N-nitro-oxazolidin-2-ones by nitration of α-amino acid derived 1,3-oxazolidin-2-ones containing one or two stereogenic centers with dinitrogen pentoxide in liquefied 1,1,1,2-tetrafluoroethane medium has been developed. The obtained N-nitroheterocycles were converted into enantiomerically pure O-(β-nitraminoalkyl) carbamates by treatment with ammonia or amines in the same solvent. The synthesized N-nitro compounds are slightly toxic in vitro to Human Embryonic Kidney 293 (HEK293) cells.

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12

Walter, Magnus W., Neh Thaker, Jack E. Baldwin, Matthias Müller, and Christopher J. Schofield. "The reaction of Tms-Cf3 with Amino Acid Derived Ring-Templates: Studies with Oxazin-2-Ones and Oxazolidin-5-Ones." Journal of Chemical Research 2000, no. 7 (2000): 310–11. http://dx.doi.org/10.3184/030823400103167606.

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13

Ciclosi, Marco, Cristiana Fava, Roberta Galeazzi, Mario Orena, Maria Eugenia González-Rosende, and José Sepúlveda-Arques. "Homochiral oxazolidin-2-ones and imidazolidin-2-ones by tandem nucleophilic addition–conjugate addition." Tetrahedron: Asymmetry 15, no. 12 (2004): 1937–43. http://dx.doi.org/10.1016/j.tetasy.2004.05.006.

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14

Xu, Daqiang, and K. Barry Sharpless. "A simple route to enantiomerically enriched oxazolidin-2-ones." Tetrahedron Letters 34, no. 6 (1993): 951–52. http://dx.doi.org/10.1016/s0040-4039(00)77462-4.

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15

Rastogi, S. K., G. K. Srivastava, S. K. Singh, R. K. Grover, R. Roy, and B. Kundu. "Solid phase synthesis of 3,5-disubstituted oxazolidin-2-ones." Tetrahedron Letters 43, no. 46 (2002): 8327–30. http://dx.doi.org/10.1016/s0040-4039(02)02009-9.

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16

Viti, Giovanni, Rossano Nannicini, and Vittorio Pestellini. "A new synthesis of oxazolidin-2-ones from trifluroacetamides." Tetrahedron Letters 33, no. 3 (1992): 377–80. http://dx.doi.org/10.1016/s0040-4039(00)74136-0.

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17

Feroci, Marta, Achille Inesi, Leucio Rossi, and Giovanni Sotgiu. "Electrochemically Induced N-Acryloylation of Chiral Oxazolidin-2-ones." European Journal of Organic Chemistry 2001, no. 14 (2001): 2765–69. http://dx.doi.org/10.1002/1099-0690(200107)2001:14<2765::aid-ejoc2765>3.0.co;2-c.

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18

Hu, Nan X., Yoshio Aso, Tetsuo Otsubo, and Fumio Ogura. "Organotellurium-mediated synthesis of oxazolidin-2-ones from alkenes." Journal of the Chemical Society, Chemical Communications, no. 19 (1987): 1447. http://dx.doi.org/10.1039/c39870001447.

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19

GEFFKEN, D., and C. HOLST. "ChemInform Abstract: 4-Hydrazono-oxazolidin-2-ones from 2-Substituted Glycolamidrazones." ChemInform 26, no. 16 (1995): no. http://dx.doi.org/10.1002/chin.199516150.

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20

Lobanova, N. A., E. Kh Sadykov, and V. K. Stankevich. "Reaction of 2-{[2-(ethenyloxy)ethoxy]methyl}oxirane with oxazolidin-2-ones." Russian Journal of Organic Chemistry 52, no. 4 (2016): 553–57. http://dx.doi.org/10.1134/s1070428016040138.

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21

Cheng, Bin-Bin, Bing Yu, and Chang-Wen Hu. "Indirect conversion of ambient pressure CO2 into oxazolidin-2-ones by a copper-based magnetic nanocatalyst." RSC Advances 6, no. 90 (2016): 87179–87. http://dx.doi.org/10.1039/c6ra15857a.

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22

Qin, Jian-Feng, Bing Wang, and Guo-Qiang Lin. "Silver(i)-catalysed carboxylative cyclisation of primary propargylic amines in neat water using potassium bicarbonate as a carboxyl source: an environment-friendly synthesis of Z-5-alkylidene-1,3-oxazolidin-2-ones." Green Chemistry 21, no. 17 (2019): 4656–61. http://dx.doi.org/10.1039/c9gc01650c.

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23

Yang, Bin, Kantapat Chansaenpak, Hongmiao Wu, et al. "Silver-promoted (radio)fluorination of unsaturated carbamates via a radical process." Chemical Communications 53, no. 24 (2017): 3497–500. http://dx.doi.org/10.1039/c7cc01393k.

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The intramolecular fluorocyclization of unsaturated carbamates proceeds via a cyclization/1,2-(hetero)aryl migration/fluorination cascade involving an unusual radical process, and provides a straightforward access to (radio)fluorinated oxazolidin-2-ones, oxazolidine-2,4-diones and 1,3-oxazinan-2-ones.

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24

Bouzina, Abdeslem, Ismahen Grib, Khaoula Bechlem, Billel Belhani, Nour-Eddine Aouf, and Malika Berredjem. "Efficient synthesis of novel N-acylsulfonamide oxazolidin-2-ones derivatives." Karbala International Journal of Modern Science 2, no. 2 (2016): 98–103. http://dx.doi.org/10.1016/j.kijoms.2016.02.003.

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25

Bratulescu, George. "An Excellent Procedure for the Synthesis of Oxazolidin-2-ones." Synthesis 2007, no. 20 (2007): 3111–12. http://dx.doi.org/10.1055/s-2007-990789.

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26

Takacs, James M., Mohamad R. Jaber, and A. Samuel Vellekoop. "Preparation of Chiral Oxazolidin-2-ones and Vicinal Amino Alcohols." Journal of Organic Chemistry 63, no. 8 (1998): 2742–48. http://dx.doi.org/10.1021/jo9720804.

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27

Feroci, Marta, Achille Inesi, Laura Palombi, Leucio Rossi, and Giovanni Sotgiu. "Electrogenerated Base-Induced N-Acylation of Chiral Oxazolidin-2-ones." Journal of Organic Chemistry 66, no. 18 (2001): 6185–88. http://dx.doi.org/10.1021/jo010038+.

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28

Gupta, Radhika, Manavi Yadav, Rashmi Gaur, Gunjan Arora, and Rakesh Kumar Sharma. "A straightforward one-pot synthesis of bioactive N-aryl oxazolidin-2-ones via a highly efficient Fe3O4@SiO2-supported acetate-based butylimidazolium ionic liquid nanocatalyst under metal- and solvent-free conditions." Green Chemistry 19, no. 16 (2017): 3801–12. http://dx.doi.org/10.1039/c7gc01414g.

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29

García-Domínguez, Patricia, Lorenz Fehr, Giulia Rusconi, and Cristina Nevado. "Palladium-catalyzed incorporation of atmospheric CO2: efficient synthesis of functionalized oxazolidinones." Chemical Science 7, no. 6 (2016): 3914–18. http://dx.doi.org/10.1039/c6sc00419a.

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30

Wang, RuiJia, Huaxu Zou, Yi Xiong, Niannian Yi, Wei Deng, and Jiannan Xiang. "PhI(OAc)2-mediated 1,2-aminohalogenation of alkynes: a general access to (E)-4-(halomethylene)oxazolidin-2-ones." Organic & Biomolecular Chemistry 15, no. 18 (2017): 3964–67. http://dx.doi.org/10.1039/c7ob00509a.

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A new PhI(OAc)<sub>2</sub>-mediated 1,2-aminohalogenation of prop-2-yn-1-yl carbamates and halogen sources is presented with excellent selectivity. The reaction is general for the construction of (E)-4-(halomethylene)oxazolidin-2-ones through the three-membered ring or N-radical.

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31

Bresciani, Giulio, Stefano Zacchini, Fabio Marchetti, and Guido Pampaloni. "Non-precious metal carbamates as catalysts for the aziridine/CO2 coupling reaction under mild conditions." Dalton Transactions 50, no. 15 (2021): 5351–59. http://dx.doi.org/10.1039/d1dt00525a.

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A novel Nb<sup>+V</sup> complex emerged as an effective homogeneous catalysts for aziridine/CO<sub>2</sub> coupling to afford 5-aryl-oxazolidin-2-ones with small N-substituents under ambient conditions.

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32

Girniene, Jolanta, Arnaud Tatibouët, Algirdas Sackus, Jing Yang, Geoffrey D. Holman, and Patrick Rollin. "Inhibition of the d-fructose transporter protein GLUT5 by fused-ring glyco-1,3-oxazolidin-2-thiones and -oxazolidin-2-ones." Carbohydrate Research 338, no. 8 (2003): 711–19. http://dx.doi.org/10.1016/s0008-6215(03)00007-7.

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33

Teran, Adrian Ochoa, та Ignacio A. Rivero. "Synthesis of enantiopure 1,3-oxazolidin-2-ones from α-dibenzylamino esters". Arkivoc 2008, № 14 (2008): 330–43. http://dx.doi.org/10.3998/ark.5550190.0009.e30.

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34

Bach, Jordi, Steven D. Bull, Stephen G. Davies, Rebecca L. Nicholson, Hitesh J. Sanganee, and Andrew D. Smith. "N-acyl-5,5-dimethyl-oxazolidin-2-ones as latent aldehyde equivalents." Tetrahedron Letters 40, no. 36 (1999): 6677–80. http://dx.doi.org/10.1016/s0040-4039(99)01345-3.

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35

Trost, Barry M., and Anantha R. Sudhakar. "A stereoselective contrasteric conversion of epoxides to cis-oxazolidin-2-ones." Journal of the American Chemical Society 110, no. 23 (1988): 7933–35. http://dx.doi.org/10.1021/ja00231a085.

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36

Rmedi, H., M. Beji, and A. Baklouti. "Synthese des Aroxy(alcoxy)sulfonyl-5-F-hexyl Oxazolidin-2-ones." Phosphorus, Sulfur, and Silicon and the Related Elements 182, no. 2 (2007): 349–56. http://dx.doi.org/10.1080/10426500600919447.

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37

Gagosz, Fabien, and Andrea Buzas. "Gold(I)-Catalyzed Formation of 5-Methylene-1,3-oxazolidin-2-ones." Synlett 2006, no. 17 (2006): 2727–30. http://dx.doi.org/10.1055/s-2006-950253.

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38

Cwik, Agnieszka, Aliz Fuchs, Zoltán Hell, Ildikó Böjtös, Dóra Halmai, and Petra Bombicz. "Modified Mg : Al hydrotalcite in the synthesis of oxazolidin-2-ones." Org. Biomol. Chem. 3, no. 6 (2005): 967–69. http://dx.doi.org/10.1039/b418848a.

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39

Seneci, Pierfausto, Marco Caspani, Franca Ripamonti, and Romeo Ciabatti. "Synthesis and antimicrobial activity of oxazolidin-2-ones and related heterocycles." Journal of the Chemical Society, Perkin Transactions 1, no. 16 (1994): 2345. http://dx.doi.org/10.1039/p19940002345.

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40

XU, D., and K. B. SHARPLESS. "ChemInform Abstract: A Simple Route to Enantiomerically Enriched Oxazolidin-2-ones." ChemInform 24, no. 27 (2010): no. http://dx.doi.org/10.1002/chin.199327185.

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41

VITI, G., R. NANNICINI, and V. PESTELLINI. "ChemInform Abstract: A New Synthesis of Oxazolidin-2-ones from Trifluoroacetamides." ChemInform 23, no. 33 (2010): no. http://dx.doi.org/10.1002/chin.199233179.

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42

Feroci, Marta, Achille Inesi, Leucio Rossi, and Giovanni Sotgiu. "ChemInform Abstract: Electrochemically Induced N-Acryloylation of Chiral Oxazolidin-2-ones." ChemInform 33, no. 12 (2010): no. http://dx.doi.org/10.1002/chin.200212158.

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43

Feroci, Marta, Achille Inesi, Laura Palombi, and Giovanni Sotgiu. "Electrogenerated Base-Induced N-Acylation of Chiral Oxazolidin-2-ones. 21." Journal of Organic Chemistry 67, no. 5 (2002): 1719–21. http://dx.doi.org/10.1021/jo016323a.

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44

Bogolyubov, A. A., N. B. Chernysheva, V. V. Nesterov, M. Yu Antipin, and V. V. Semenov. "Dehydration of 4-hydroxy-4-methyl-3-phenylamino-oxazolidin-2-ones." Chemistry of Heterocyclic Compounds 40, no. 10 (2004): 1305–9. http://dx.doi.org/10.1007/s10593-005-0064-0.

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45

Sepúlveda-Arques, José, Trinidad Armero-Alarte, Alberto Acero-Alarcón, Elena Zaballos-Garcia, Belén Yruretagoyena Solesio, and Jesús Ezquerra Carrera. "Stereoselective ring transformation of n-alkyl aziridines into oxazolidin-2-ones." Tetrahedron 52, no. 6 (1996): 2097–102. http://dx.doi.org/10.1016/0040-4020(95)01025-4.

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46

Shaye, Najla Al, David M. Benoit, Sameer Chavda, et al. "Resolution of pentafluorophenyl 2-phenylpropanoate using combinations of quasi-enantiomeric oxazolidin-2-ones." Tetrahedron: Asymmetry 22, no. 4 (2011): 413–38. http://dx.doi.org/10.1016/j.tetasy.2011.02.022.

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47

Sheng, Shou‐Ri, Hai‐Rong Luo, Zhen‐Zhong Huang, Wu‐Kang Sun, and Xiao‐Ling Liu. "Facile One‐Pot Synthesis of Oxazolidin‐2‐ones from Phenyl 2‐Hydroxyalkyl Selenides." Synthetic Communications 37, no. 16 (2007): 2693–99. http://dx.doi.org/10.1080/00397910701465420.

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48

Falb, Eliezer, Abraham Nudelman, and Alfred Hassner. "A Convenient Synthesis of Chiral Oxazolidin-2-Ones and Thiazolidin-2-Ones and an Improved Preparation of Triphosgene." Synthetic Communications 23, no. 20 (1993): 2839–44. http://dx.doi.org/10.1080/00397919308012605.

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49

Belovezhets, L. A., N. A. Lobanova, E. Kh Sadykov, and V. K. Stankevich. "N-SUBSTITUTED 5-{[2-(VINYLOXY)ETHOXY]METHYL}-1,3-OXAZOLIDIN-2-ONES –NEW ANTIBACTERIAL AGENTS." Proceedings of universities. Applied chemistry and biotechnology 6, no. 3 (2016): 21–25. http://dx.doi.org/10.21285/2227-2925-2016-6-3-21-25.

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50

Feroci, Marta, Achille Inesi, Laura Palombi, and Giovanni Sotgiu. "ChemInform Abstract: Electrogenerated Base-Induced N-Acylation of Chiral Oxazolidin-2-ones. Part 2." ChemInform 33, no. 33 (2010): no. http://dx.doi.org/10.1002/chin.200233071.

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