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Journal articles on the topic 'Isoxazolidinones'

Author: Grafiati

Published: 4 June 2021

Last updated: 3 February 2022

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1

Cao, Xuefei, Amjad Iqbal, Amit Patel та ін. "3-Alkoxy-5-isoxazolidinones mimic β-lactams". Biochemical and Biophysical Research Communications 311, № 2 (2003): 267–71. http://dx.doi.org/10.1016/j.bbrc.2003.09.210.

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2

Lee, Hee-Seung, Jin-Seong Park, Byeong Moon Kim та Samuel H. Gellman. "Efficient Synthesis of Enantiomerically Pure β2-Amino Acids via Chiral Isoxazolidinones". Journal of Organic Chemistry 68, № 4 (2003): 1575–78. http://dx.doi.org/10.1021/jo026738b.

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3

Luisi, Renzo, Vito Capriati, Saverio Florio та Teresa Vista. "New Synthesis of Optically Active 5-Isoxazolidinones and β-Amino Acids". Journal of Organic Chemistry 68, № 25 (2003): 9861–64. http://dx.doi.org/10.1021/jo035356i.

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4

Tite, Tony, Mohamad Sabbah, Vincent Levacher, and Jean-François Brière. "Organocatalysed decarboxylative protonation process from Meldrum's acid: enantioselective synthesis of isoxazolidinones." Chemical Communications 49, no. 98 (2013): 11569. http://dx.doi.org/10.1039/c3cc47695b.

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5

Tolomelli, Alessandra, Giuliana Cardillo, Luca Gentilucci, Riccardo Juris, Angelo Viola, and Eusebio Juaristi. "Exploring the reactivity of alkylidene malonamides: synthesis of polyfunctionalized isoxazolidinones, aziridines and oxazolines." Arkivoc 2012, no. 5 (2012): 196–209. http://dx.doi.org/10.3998/ark.5550190.0013.518.

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6

Tite, Tony, Mohamad Sabbah, Vincent Levacher, and Jean-Francois Briere. "ChemInform Abstract: Organocatalyzed Decarboxylative Protonation Process from Meldrum′s Acid: Enantioselective Synthesis of Isoxazolidinones." ChemInform 45, no. 17 (2014): no. http://dx.doi.org/10.1002/chin.201417140.

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7

Prakash, G. K. Surya, Zhe Zhang, Fang Wang, et al. "Stereoselective Synthesis of Fluoroalkenoates and Fluorinated Isoxazolidinones: N-Substituents Governing the Dual Reactivity of Nitrones." Chemistry - A European Journal 20, no. 3 (2013): 831–38. http://dx.doi.org/10.1002/chem.201303509.

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8

Tabarki, Mohamed Ali, та Rafâa Besbes. "Regioselective ring opening of β-phenylglycidate and aziridine-2-carboxylates with N-alkylhydroxylamines: synthesis of isoxazolidinones". Tetrahedron 70, № 5 (2014): 1060–64. http://dx.doi.org/10.1016/j.tet.2013.12.052.

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9

Eichinger, Karl, Mohammad RezaRostami, and Florian Sieder. "A Novel Base Promoted Reaction of Methyl 2-Isoxazoline-5-acetates to 5-(2-oxoethyl)-3-isoxazolidinones." Synthetic Communications 28, no. 13 (1998): 2457–66. http://dx.doi.org/10.1080/00397919808004297.

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10

Prakash, G. K. Surya, Zhe Zhang, Fang Wang, et al. "ChemInform Abstract: Stereoselective Synthesis of Fluoroalkenoates and Fluorinated Isoxazolidinones: N-Substituents Governing the Dual Reactivity of Nitrones." ChemInform 45, no. 28 (2014): no. http://dx.doi.org/10.1002/chin.201428118.

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11

Brar, Amandeep, Daniel K. Unruh, Natalie Ling, and Clemens Krempner. "BPh3-Catalyzed [2+3] Cycloaddition of Ph3PCCO with Aldonitrones: Access to 5-Isoxazolidinones with Exocyclic Phosphonium Ylide Moieties." Organic Letters 21, no. 16 (2019): 6305–9. http://dx.doi.org/10.1021/acs.orglett.9b02192.

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12

ZELENIN, K. N., I. P. BEZHAN, and I. V. LAGODA. "ChemInform Abstract: 5(3)-Hydroxy-3(5)-isoxazolidinones and 5-Hydroxy-3-pyrazolidinones and Their Ring-Chain Tautomerism." ChemInform 23, no. 8 (2010): no. http://dx.doi.org/10.1002/chin.199208206.

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13

Tabarki, Mohamed Ali, та Rafaa Besbes. "ChemInform Abstract: Regioselective Ring Opening of β-Phenylglycidate and Aziridine-2-carboxylates with N-Alkylhydroxylamines: Synthesis of Isoxazolidinones." ChemInform 45, № 29 (2014): no. http://dx.doi.org/10.1002/chin.201429153.

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14

EICHINGER, K., M. R. ROSTAMI, and F. SIEDER. "ChemInform Abstract: A Novel Base Promoted Reaction of Methyl 2-Isoxazoline-5-acetates to 5-(2-Oxoethyl)-3-isoxazolidinones." ChemInform 29, no. 40 (2010): no. http://dx.doi.org/10.1002/chin.199840121.

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15

ISHIKAWA, T., K. NAGAI, T. KUDOH та S. SAITO. "ChemInform Abstract: Asymmetric Synthesis of Substituted Isoxazolidinones from α,. beta.-Unsaturated Esters and Hydroxylamines by Means of Double Stereodifferentiation." ChemInform 27, № 16 (2010): no. http://dx.doi.org/10.1002/chin.199616156.

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16

Kalhor, Mehdi, Seyed Mehdi Sajjadi, and Akbar Dadras. "Cu/TCH-pr@SBA-15 nano-composite: a new organometallic catalyst for facile three-component synthesis of 4-arylidene-isoxazolidinones." RSC Advances 10, no. 46 (2020): 27439–46. http://dx.doi.org/10.1039/d0ra01314e.

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A copper complex supported on SBA-15 nanoparticles (Cu/TCH-pr@SBA-15) was synthesized by the post-synthesis modification of mesoporous silica with (OEt)<sub>3</sub>Si-(CH<sub>2</sub>)<sub>3</sub>Cl and thiocarbohydrazide (TCH) and subsequent metal–ligand coordination with Cu(ii).

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17

Shindo, Mitsuru, Kotaro Itoh, Chinatsu Tsuchiya та Kozo Shishido. "Anionic Inverse Electron-Demand 1,3-Dipolar Cycloaddition of Nitrones with Ynolates. Facile Stereoselective Synthesis of 5-Isoxazolidinones Leading to β-Amino Acids". Organic Letters 4, № 18 (2002): 3119–21. http://dx.doi.org/10.1021/ol0264455.

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18

Shirsale, Ashwini, Yogesh Patil, Girish Rawal, et al. "A Convenient and Concise Metal-Free Approach to Functionalized Bicyclic Pyrimidinones from Oxazine-2,6-diones." Synthesis 50, no. 10 (2018): 2087–93. http://dx.doi.org/10.1055/s-0037-1609364.

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The synthesis of previously unreported pyrazolo-pyrimidinones and isoxazolo-pyrimidinones are achieved via metal-free coupling of oxazine-2,6-diones with pyrazolidinone and isoxazolidinone, respectively. The synthesis provides easy access to a variety of novel 2-dimensional building blocks that can be derivatized to generate a range of drug- and agro-like molecules.

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19

Brunton, David J., Gurjeet Gill, and Christopher Preston. "Resistance to bixlozone and clomazone in cross-resistant rigid ryegrass (Lolium rigidum) populations from southern Australia." Weed Science 69, no. 3 (2021): 284–89. http://dx.doi.org/10.1017/wsc.2021.6.

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AbstractThree resistant (R) rigid ryegrass (Lolium rigidum Gaudin) populations from southern Australia (EP162, 375-14, and 198-15) with cross-resistance to thiocarbamate, chloroacetamide, and sulfonylisoxazoline herbicides displayed reduced sensitivity to the isoxazolidinone herbicides bixlozone and clomazone. Each of these R populations was exposed to two cycles of recurrent selection (RS) in which plants were treated with the field rate of bixlozone, survivors were bulk crossed, and seed was collected. After the first cycle of recurrent selection (RS1), the LD50 to bixlozone in population 19

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20

Sibi, Mukund P., Brandon Gustafson, and Julien Coulomb. "3-Isoxazolidinone: A New Achiral Template for Enantioselective Transformations." Bulletin of the Korean Chemical Society 31, no. 3 (2010): 541–42. http://dx.doi.org/10.5012/bkcs.2010.31.03.541.

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21

Lützow, Manfred, Peter Beyer, and Hans Kleinig. "The Herbicide Command Does Not Inhibit the Prenyl Diphosphate-Forming Enzymes in Plastids." Zeitschrift für Naturforschung C 45, no. 7-8 (1990): 856–58. http://dx.doi.org/10.1515/znc-1990-7-818.

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Abstract The herbicide Comm and (2-(2-chlorophenyl)methyl-4,4-dimethyl-3-isoxazolidinone) does not affect the in vitro activities of the plastid enzymes catalyzing the steps leading from isopen tenyl diphosphate to geranylgeranyl diphosphate and phytoene, i.e. the isopentenyl diphos phate isomerase, prenyl transferase and phytoene synthase. The extractable activities of these enzymes in herbicide-treated seedlings are also not affected. Nevertheless, the synthesis of chlorophylls and carotenoids in treated seedlings is severely inhibited in vivo. The mode of action of Comm and remains still

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22

Shamsuzzaman, Hena Khanam, Ashraf Mashrai, and Nazish Siddiqui. "Construction of novel steroidal isoxazolidinone derivatives under Vilsmeier–Haack conditions." Tetrahedron Letters 54, no. 8 (2013): 874–77. http://dx.doi.org/10.1016/j.tetlet.2012.11.105.

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23

GAO, F., G. ZHANG, L. ZHENG, Y. LI, and S. ZHANG. "Synthesis and Characterization of Novel 4-Methyl-3-isoxazolidinone Derivatives." Chemical Research in Chinese Universities 22, no. 6 (2006): 717–20. http://dx.doi.org/10.1016/s1005-9040(06)60197-9.

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24

Sibi, Mukund P., Brandon Gustafson, and Julien Coulomb. "ChemInform Abstract: 3-Isoxazolidinone: A New Achiral Template for Enantioselective Transformations." ChemInform 41, no. 32 (2010): no. http://dx.doi.org/10.1002/chin.201032032.

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25

Rodrigues, Benedito N. "Influência da cobertura morta no comportamento dos herbicidas imazaquin e clomazone." Planta Daninha 11, no. 1-2 (1993): 21–28. http://dx.doi.org/10.1590/s0100-83581993000100004.

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Experimentos de campo e bioensaios em casa-de-vegetação foram realizados para se estudar a influência da cobertura morta de trigo (Triticum aestivum L.) no comportamento dos herbicidas imazaquin {ácido 2-[4,5 dihidro-4-metil-4-(1-metiletil)-5-oxo-1H-imidazol-2-ilo]-3-quinolinacarboxílico} e clomazone {2-[(2-clorofenil)metil]-4,4-dimetil-3-isoxazolidinona}, aplicados em pré-emergência na cultura da soja [Glycine max (L.) Merril], no sistema de plantio direto. O clomazone mostrou evidências de ter sido interceptado pela cobertura morta. A presença da cobertura morta não influiu na retenção do im

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26

Al-Hazmi, F. S., A. A. Al-Ghamdi, Gary W. Beall, Lyudmila M. Bronstein, and Waleed E. Mahmoud. "Synthesis and characterization of 4-amino-3-isoxazolidinone intercalated NiAl-LDH for nanocarrier applications." Colloids and Surfaces A: Physicochemical and Engineering Aspects 485 (November 2015): 91–95. http://dx.doi.org/10.1016/j.colsurfa.2015.09.011.

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27

Overy, David, Kathleen Calati, Jennifer Nielsen Kahn, et al. "Isolation and structure elucidation of parnafungins C and D, isoxazolidinone-containing antifungal natural products." Bioorganic & Medicinal Chemistry Letters 19, no. 4 (2009): 1224–27. http://dx.doi.org/10.1016/j.bmcl.2008.12.081.

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28

Dehmlow, Eckehard Volker, Jörg Bollhöfer, and Gorden Thye. "Regioselective alkylation of anthrone, 5,5-dimethyl-3-isoxazolidinone and 4-methylquinolone by phase transfer catalysis." Journal of Chemical Research 2001, no. 3 (2001): 113–15. http://dx.doi.org/10.3184/030823401103169171.

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29

Grey, Timothy L., David C. Bridges, and D. Scott NeSmith. "Tolerance of Cucurbits to the Herbicides Clomazone, Ethalfluralin and Pendimethalin. II. Watermelon." HortScience 35, no. 4 (2000): 637–41. http://dx.doi.org/10.21273/hortsci.35.4.637.

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Field studies were conducted in 1993, 1994, and 1995 to determine tolerance of seeded and transplanted watermelon [Citrullus lanatus (Thunb.) Matsum and Nak.] to clomazone, ethalfluralin, and pendimethalin using method of stand establishment (directseeded vs. transplanted) and time of herbicide application [preplant soil incorporated (PPI), preplant to the surface (PP), or postplant to the surface (POP)] as variables. Yield and average fruit weight in plots with clomazone were equal to or greater than those in control plots for the 3-year study regardless of method of application. Bleaching an

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30

Grey, Timothy L., David C. Bridges, and D. Scott NeSmith. "Response of Several Transplanted Pepper Cultivars to Variable Rates and Methods of Application of Clomazone." HortScience 36, no. 1 (2001): 104–6. http://dx.doi.org/10.21273/hortsci.36.1.104.

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Field studies were conducted to evaluate the tolerance of several pepper (Capsicum annuum L.) cultivars to the herbicide clomazone. Peppers tested included the bell cultivars Yolo Wonder and Jupiter; the banana cultivar Sweet Banana; and the pungent cultivars Jalapeno and Red Chili. Treatments were clomazone at 0.56 or 1.12 kg·ha-1 a.i. applied either preplant incorporated (PPI), pretransplant (PRE-T), or posttransplant (POS-T) on the day of transplanting, plus a nontreated control. Clomazone at 1.12 kg·ha-1 a.i. PPI and PRE-T significantly injured (bleaching or chlorosis of foliage) `Sweet Ba

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31

Juarez-Garcia, M. Elisa, Shouyun Yu та Jeffrey W. Bode. "Asymmetric synthesis of enantiopure isoxazolidinone monomers for the synthesis of β3-oligopeptides by chemoselective amide ligation". Tetrahedron 66, № 26 (2010): 4841–53. http://dx.doi.org/10.1016/j.tet.2010.04.016.

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32

Ishikawa, Teruhiko, Keita Nagai, Takayuki Kudoh та Seiki Saito. "Asymmetric Synthesis of Substituted Isoxazolidinone from α,β-Unsaturated Esters and Hydroxylamines by means of Double Stereodifferentiation". Synlett 1995, № 11 (1995): 1171–73. http://dx.doi.org/10.1055/s-1995-5228.

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33

Dehmlow, Eckehard Volker, Joerg Bollhoefer, and Gorden Thye. "ChemInform Abstract: Regioselective Alkylation of Anthrone, 5,5-Dimethyl-3-isoxazolidinone and 4-Methylquinolone by Phase Transfer Catalysis." ChemInform 32, no. 38 (2010): no. http://dx.doi.org/10.1002/chin.200138023.

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34

Harrison, Howard F., Chandrasekar S. Kousik, and Amnon Levi. "Identification of Citrullus lanatus Germplasm Accessions Tolerant to Clomazone Herbicide." HortScience 46, no. 5 (2011): 684–87. http://dx.doi.org/10.21273/hortsci.46.5.684.

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Clomazone herbicide is registered for use in watermelon; however, crop tolerance is marginal, and the recommended use rates (0.17 to 0.28 kg a.i./ha) are lower for watermelon than for other crops. In a greenhouse germplasm evaluation experiment including 56 germplasm accessions and watermelon cultivars, three Citrullus lanatus var. citroides PI accessions (PI 482324, PI 5003540, and PI 532624) were not injured by clomazone, whereas most of the other accessions and cultivars were moderately or severely injured. A greenhouse concentration response experiment demonstrated that the clomazone conce

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35

Khodayari, Khosro, Roy J. Smith, and Howard L. Black. "Red Rice (Oryza sativa) Control with Herbicide Treatments in Soybeans (Glycine max)." Weed Science 35, no. 1 (1987): 127–29. http://dx.doi.org/10.1017/s0043174500026916.

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Preplant incorporation of alachlor [2-chloro-N-(2,6-diethylphenyl)-N-(methoxymethyl)acetamide] at 3.6 kg ai/ha, metolachlor [2-chloro-N-(2-ethyl-6-methylphenyl)-N-(2-methoxy-1-methylethyl)acetamide] at 2.2 kg ai/ha, and tank mixtures of imazaquin {2-[4,5-dihydro-4-methyl-4-(1-methylethyl)-5-oxo-1H-imidazol-2-yl]-3-quinolinecarboxylic acid} with either alachlor at 0.14 + 2.2 kg ai/ha or metolachlor at 0.14 + 1.1 kg ai/ha controlled >90% red rice (Oryza sativaL. # ORYSA) in soybeans [Glycine max(L.) Merr.]. Also, FMC-57020 [2-(2-chlorophenyl)methyl-4,4-dimethyl-3-isoxazolidinone] at 1.7 kg ai

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36

Hostettler, Bernhard, Jean Pierre Obrecht, Roland Prewo, Jost H. Bieri, and Heinz Heimgartner. "5,6,7,8-Tetrahydro-4H-1,2,5-oxadiazocin-6-one durch Ringerweiterung nach Addition eines 3-Isoxazolidinons mit 3-Amino-2H-azirinen." Helvetica Chimica Acta 69, no. 2 (1986): 298–304. http://dx.doi.org/10.1002/hlca.19860690207.

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37

Ferrazzano, Lucia, Angelo Viola, Elena Lonati та ін. "New isoxazolidinone and 3,4-dehydro-β-proline derivatives as antibacterial agents and MAO-inhibitors: A complex balance between two activities". European Journal of Medicinal Chemistry 124 (листопад 2016): 906–19. http://dx.doi.org/10.1016/j.ejmech.2016.09.007.

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38

Lanza, Giuseppe, Maria A. Chiacchio, Salvatore V. Giofrè, Roberto Romeo та Pedro Merino. "The High Selectivity of the Cp2ZrHCl Reducing Agent for Imides: A Combined Experimental and Theoretical Study on γ-Lactam and Isoxazolidinone Derivatives". European Journal of Organic Chemistry 2013, № 1 (2012): 95–104. http://dx.doi.org/10.1002/ejoc.201201186.

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39

Grey, Timothy L., David C. Bridges, and D. Scott NeSmith. "Tolerance of Cucurbits to the Herbicides Clomazone, Ethalfluralin, and Pendimenthalin. I. Summer Squash." HortScience 35, no. 4 (2000): 632–36. http://dx.doi.org/10.21273/hortsci.35.4.632.

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Field studies were conducted in 1993, 1994, and 1996 to determine the tolerance of several cultivars of zucchini and yellow crookneck squash (Cucurbita pepo L.) to various rates and methods of application of clomazone, ethalfluralin, and pendimethalin. Applying herbicides preplant soil incorporated (PPI), preemergence (PRE), at seedling emergence (SE), or early postemergence (EPOT) resulted in plant injury that varied from 0% to 98%. Ethalfluralin and pendimethalin (PPI) at 1.12 kg·ha–1 a.i. resulted in the greatest stand and yield reductions across all cultivars. Fruit number and weight decli

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40

Guo-Feng, Zhao, Jin Gui-Yu, Liu Zhong-Fa, Ren Jun, and Li Yu-Chang. "Synthesis and biological activity of new heterocyclic compounds 5-[(1,l-dimethyl)ethyl]-3-aryl-(1H-1,2,3-triazol-1-yl)-5-isoxazolidinols." Chinese Journal of Chemistry 16, no. 4 (2010): 363–66. http://dx.doi.org/10.1002/cjoc.19980160411.

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41

Herrera, Juan Manuel Arrieta. "Aspectos sobre el control de malezas compuestas en pastos dedicados a la ganadería de leche." Corpoica Ciencia y Tecnología Agropecuaria 5, no. 1 (2004): 76. http://dx.doi.org/10.21930/rcta.vol5_num1_art:29.

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<p>Con el objeto de encontrar métodos de control oportunos y eficientes de <em>Senecio inaequidens </em>y <em>Sonchus oleraceus</em>, se desarrollaron una serie de observaciones sobre la ecofisiología y morfología de estas especies de malezas y se probaron algunos métodos de control cultural, químico y biológico. Los resultados mostraron que la edad de la semilla, la cantidad y calidad de la luz percibida, tienen una incidencia proporcional sobre la tasa de germinación. La relación entre la temperatura día/noche es inversamente proporcional a la producción de capí

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42

"Isoxazolidinones via Asymmetric Decarboxylative Protonation." Synfacts 10, no. 01 (2013): 0086. http://dx.doi.org/10.1055/s-0033-1340410.

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43

Luisi, Renzo, Vito Capriati, Saverio Florio та Teresa Vista. "New Synthesis of Optically Active 5-Isoxazolidinones and β-Amino Acids." ChemInform 35, № 17 (2004). http://dx.doi.org/10.1002/chin.200417116.

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44

Piperno, Anna, Ugo Chiacchio, Daniela Iannazzo, Salvatore V. Giofre, Giovanni Romeo, and Roberto Romeo. "First Example of Direct RuO4-Catalyzed Oxidation of Isoxazolidinones to 3-Isoxazolidones." ChemInform 38, no. 36 (2007). http://dx.doi.org/10.1002/chin.200736112.

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45

CHANG, J. H., M. J. KONZ, E. A. ALY, et al. "ChemInform Abstract: 3-Isoxazolidinones and Related Compounds: A New Class of Herbicides." ChemInform 19, no. 28 (1988). http://dx.doi.org/10.1002/chin.198828302.

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46

Kalhor, Mehdi, Sima Samiei, and Seyed Ahmad Mirshokraie. "MnO2@Zeolite-Y Nanoporous: Preparation and Application as a High Efficient Catalyst for Multi-Component Synthesis of 4-Arylidene-Isoxazolidinones." Silicon, April 10, 2020. http://dx.doi.org/10.1007/s12633-020-00413-5.

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47

Shindo, Mitsuru, Kotaro Itoh, Chinatsu Tsuchiya та Kozo Shishido. "Anionic Inverse Electron-Demand 1,3-Dipolar Cycloaddition of Nitrones with Ynolates. Facile Stereoselective Synthesis of 5-Isoxazolidinones Leading to β-Amino Acids." ChemInform 34, № 3 (2003). http://dx.doi.org/10.1002/chin.200303105.

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48

Overy, David, Kathleen Calati, Jennifer Nielsen Kahn, et al. "ChemInform Abstract: Isolation and Structure Elucidation of Parnafungins C and D, Isoxazolidinone-Containing Antifungal Natural Products." ChemInform 40, no. 28 (2009). http://dx.doi.org/10.1002/chin.200928199.

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49

JONSSON, CLAUDIO M., ALINE DE H. N. MAIA, and CELSO J. A. FERREIRA (In memorian). "DECOMPOSIÇÃO DE Typha latifolia EM MEIO AQUÁTICO NA PRESENÇA DO HERBICIDA CLOMZONE." Pesticidas: Revista de Ecotoxicologia e Meio Ambiente 10 (December 31, 2000). http://dx.doi.org/10.5380/pes.v10i0.39661.

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O clomazone (2-(2-clorofenil) metal-4,4-dimetil-3-isoxazolidinona) é um hericida pós-emergente, amplamente utilizado em culturas de arroz irrigado no Rio Grande do Sul (Brasil), Com atividade no controle de gramíneas na sua dose recomendada de 700 g/ha. A presença deste composto na água e em sedimentos pode afetar micro-organismos responsáveis pela decomposição de matéria orgânica e consequentemente a cadeia trófica, sustentada pelos decompositores. No presente trabalho foi estimada a inibição da taxa de decomposição de matéria orgânica exposta a seis concentrações de formulação de Clomazone:

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HOSTETTLER, B., J. P. OBRECHT, R. PREWO, J. H. BIERI, and H. HEIMGARTNER. "ChemInform Abstract: 5,6,7,8-Tetrahydro-4H-1,2,5-oxadiazocin-6-ones, Ring Enlargement Products from a 3-Isoxazolidinone and 3-Amino-2H-azirines." Chemischer Informationsdienst 17, no. 24 (1986). http://dx.doi.org/10.1002/chin.198624223.

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