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Journal articles on the topic 'Phosphonomethyl'

Author: Grafiati

Published: 4 June 2021

Last updated: 10 February 2022

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1

Ying, Shao-Ming, Jun-Yue Lin, Guang-Pei Zhou, Qiu-Yan Luo, and Jian-Hong Wu. "[N-(Phosphonomethyl)ethylammonio]methylphosphonate." Acta Crystallographica Section E Structure Reports Online 63, no. 3 (February 7, 2007): o1153—o1154. http://dx.doi.org/10.1107/s1600536807004461.

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The title compound, C5H15NO6P2, exists as a zwitterion. The N atom of the amino group is protonated and one of the phosphonic acid groups is deprotonated. The molecules form hydrogen-bonded (202) layers.

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2

Krečmerová, Marcela, Hubert Hřebabecký, and Antonín Holý. "Synthesis of 5'-O-phosphonomethyl derivatives of pyrimidine 2'-deoxynucleosides." Collection of Czechoslovak Chemical Communications 55, no. 10 (1990): 2521–36. http://dx.doi.org/10.1135/cccc19902521.

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Reaction of sodium salt of 3-N,3'-O-bis(benzyloxymethyl)-2'-deoxyuridine (X) and 3-N,3'-O-bis(benzyloxymethyl)-2'-deoxythymidine (XI) with diethyl p-toluenesulfonyloxymethanephosphonate in dimethylformamide afforded diesters of the respective 5'-O-phosphonomethyl derivatives XII and XVII. Diethyl esters of 5'-O-phosphonomethyl-2'-deoxynucleosides XV and XIX, obtained after hydrogenolytic removal of the benzyloxymethyl groups, were converted into free 2'-deoxy-5'-O-phosphonomethyluridine (XVI) and a mixture of anomeric 1-(2-deoxy-5-O-phosphonomethyl-β-D-erythro-pentofuranosyl)thymines (XXIIIa, XXIIIb), respectively. Analogously, 2'-deoxy-5'-O-phosphonomethylcytidine (XXXIV) was prepared from 4-N-benzoyl-2'-deoxy-3'-O-(tetrahydro-2H-pyran-2-yl) cytidine (XXX) via diethyl ester of 2'-deoxy-5'-O-phosphonomethylcytidine (XXXIII). This compound reacted with bromotrimethylsilane to give compound XXXIV without anomerization and nucleoside bond cleavage. Condensation of the protected nucleosides X and XI with dibenzyl p-toluenesulfonyloxymethanephosphonate afforded dibenzyl esters of the corresponding 5'-O-phosphonomethyl derivatives XIII and XVIII. The free 5'-O-phosphonomethyl derivatives XVI and XXIIIa were obtained from XIII and XVIII by catalytic hydrogenation.

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3

Solyev, Pavel N., Maxim V. Jasko, Alla A. Kleymenova, Marina K. Kukhanova, and Sergey N. Kochetkov. "Versatile synthesis of oxime-containing acyclic nucleoside phosphonates – synthetic solutions and antiviral activity." Organic & Biomolecular Chemistry 13, no. 44 (2015): 10946–56. http://dx.doi.org/10.1039/c5ob01571e.

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New oxime-containing acyclic nucleoside phosphonates 9-{2-[(phosphonomethyl)oximino]ethyl}adenine (1), -guanine (2) and 9-{2-[(phosphonomethyl)oximino]propyl}adenine (3) with wide spectrum activity against different types of viruses were synthesized.

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4

Gavagan, John E., Susan K. Fager, John E. Seip, Dawn S. Clark, Mark S. Payne, David L. Anton, and Robert DiCosimo. "Chemoenzymic Synthesis ofN-(Phosphonomethyl)glycine." Journal of Organic Chemistry 62, no. 16 (August 1997): 5419–27. http://dx.doi.org/10.1021/jo970455f.

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5

Weichsel, A., and T. Lis. "2-(Phosphonomethyl)acrylic Acid Hemihydrate and Ammonium 2-(Phosphonomethyl)acrylate: Analogues of Phosphoenolpyruvate (PEP)." Acta Crystallographica Section C Crystal Structure Communications 52, no. 1 (January 15, 1996): 97–101. http://dx.doi.org/10.1107/s0108270195009802.

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6

Sawka-Dobrowolska, W., and J. Barycki. "Structure of N-phosphonomethyl-L-proline." Acta Crystallographica Section C Crystal Structure Communications 45, no. 4 (April 15, 1989): 606–9. http://dx.doi.org/10.1107/s0108270188010236.

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7

Gaied, Lilia Ben, Soufiane Touil, and Hedi Zantour. "Synthese de 2-Amino-5-(phosphonomethyl) Thiophenes." Phosphorus, Sulfur, and Silicon and the Related Elements 181, no. 3 (March 1, 2006): 601–8. http://dx.doi.org/10.1080/10426500500269844.

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8

Gholivand, Khodayar, and Ali Reza Farrokhi. "Poly[{μ10-[(phosphonomethyl)iminodimethylene]diphosphonato}dithallium(I)]." Acta Crystallographica Section E Structure Reports Online 66, no. 8 (July 3, 2010): m873. http://dx.doi.org/10.1107/s1600536809031006.

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9

Dupont, Nathalie, Pascal Retailleau, Evelyne Migianu-Griffoni, and Carole Barbey. "Methyl [hydroxy(phenyl)phosphonomethyl]phosphonate methanol solvate." Acta Crystallographica Section E Structure Reports Online 64, no. 10 (September 6, 2008): o1874—o1875. http://dx.doi.org/10.1107/s160053680802285x.

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10

Ferguson, G., J. F. Gallagher, W. Vogt, J. Phillips, and G. J. B. Williams. "4-Methyl-2,6-bis(phosphonomethyl)phenol dihydrate." Acta Crystallographica Section C Crystal Structure Communications 49, no. 5 (May 15, 1993): 1024–26. http://dx.doi.org/10.1107/s0108270192011685.

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11

Cunha-Silva, Luís, Fa-Nian Shi, Jacek Klinowski, Tito Trindade, João Rocha, and Filipe A. Almeida Paz. "Decaaquadioxobis[μ3-N-(phosphonomethyl)iminodiacetato]dimanganesedivanadium dihydrate." Acta Crystallographica Section E Structure Reports Online 63, no. 2 (January 10, 2007): m372—m375. http://dx.doi.org/10.1107/s1600536806054675.

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12

Adani, Fabrizio, Enzo Montoneri, and Philip J. Squattrito. "4-Fluoro-2-(phosphonomethyl)benzenesulfonic acid monohydrate." Acta Crystallographica Section C Crystal Structure Communications 56, no. 4 (April 15, 2000): 463–64. http://dx.doi.org/10.1107/s0108270100000184.

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13

Liu, Chao, Christopher Cozens, Faten Jaziri, Jef Rozenski, Amandine Maréchal, Shrinivas Dumbre, Valérie Pezo, et al. "Phosphonomethyl Oligonucleotides as Backbone-Modified Artificial Genetic Polymers." Journal of the American Chemical Society 140, no. 21 (May 3, 2018): 6690–99. http://dx.doi.org/10.1021/jacs.8b03447.

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14

Komissarov, Alexey, Dmitry Makarov, Olga Yuzhakova, Lubov Savvina, Nina Kuznetsova, Oleg Kaliya, Evgeny Lukyanets, and Vladimir Negrimovsky. "Synthesis and Some Properties of Phosphonomethyl Substituted Phthalocyanines." Macroheterocycles 5, no. 2 (2012): 169–74. http://dx.doi.org/10.6060/mhc2012.120466n.

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15

Renders, Marleen, Gert Emmerechts, Jef Rozenski, Marcela Krecmerová, Antonin Holý, and Piet Herdewijn. "Enzymatic Synthesis of Phosphonomethyl Oligonucleotides by Therminator Polymerase." Angewandte Chemie International Edition 46, no. 14 (March 26, 2007): 2501–4. http://dx.doi.org/10.1002/anie.200603435.

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16

Renders, Marleen, Gert Emmerechts, Jef Rozenski, Marcela Krecmerová, Antonin Holý, and Piet Herdewijn. "Enzymatic Synthesis of Phosphonomethyl Oligonucleotides by Therminator Polymerase." Angewandte Chemie 119, no. 14 (March 26, 2007): 2553–56. http://dx.doi.org/10.1002/ange.200603435.

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17

Taddei, Marco, Ferdinando Costantino, Fabio Marmottini, Angiolina Comotti, Piero Sozzani, and Riccardo Vivani. "The first route to highly stable crystalline microporous zirconium phosphonate metal–organic frameworks." Chem. Commun. 50, no. 94 (2014): 14831–34. http://dx.doi.org/10.1039/c4cc06223j.

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18

Riley, Dennis P., Donald L. Fields, and Willie Rivers. "Vanadium(IV,V) salts as homogeneous catalysts for the oxygen oxidation of N-(phosphonomethyl)iminodiacetic acid to N-(phosphonomethyl)glycine." Inorganic Chemistry 30, no. 22 (October 1991): 4191–97. http://dx.doi.org/10.1021/ic00022a020.

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19

Taddei, Marco, Stephen J. I. Shearan, Anna Donnadio, Mario Casciola, Riccardo Vivani, and Ferdinando Costantino. "Investigating the effect of positional isomerism on the assembly of zirconium phosphonates based on tritopic linkers." Dalton Transactions 49, no. 12 (2020): 3662–66. http://dx.doi.org/10.1039/c9dt02463h.

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Combination of the novel linker 2,4,6-tris[3-(phosphonomethyl)phenyl]-1,3,5-triazine and Zr(iv) afforded a layered compound that lacks extended inorganic connectivity and displays good proton conductivity.

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20

Bewick, Thomas A., Larry K. Binning, and Malcolm N. Dana. "Postattachment Control of Swamp Dodder (Cuscuta gronovii) in Cranberry (Vaccinium macrocarpon) and Carrot (Daucus carota)." Weed Technology 2, no. 2 (April 1988): 166–69. http://dx.doi.org/10.1017/s0890037x00030323.

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In a 3-y field study, the isopropylamine salt of glyphosate [N-(phosphonomethyl)glycine] at 1.7 kg ai/ha and sulphosate [trimethyl sulfonium salt of N-(phosphonomethyl)glycine] at three rates, a split application of 0.6 + 0.6 or single applications of 1.1 or 1.7 kg ai/ha satisfactorily controlled swamp dodder (Cuscuta gronoviiWilld. ex R. & S. # CVCGR) in cranberry (Vaccinium macrocarponAit.). While none of these treatments decreased cranberry yield, sulphosate at 1.1 or 1.7 kg/ha did increase yield. Glyphosate at 0.4 kg/ha applied late in the life cycle of carrot (Daucus carotaL.) when swamp dodder was in full flower satisfactorily controlled swamp dodder while increasing yield of carrot roots. Glyphosate applied early in the life cycle of carrot and dodder controlled swamp dodder but lowered yield of carrot roots.

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21

Lattuada, Luciano, Giovanni B. Giovenzana, Fabio Travagin, and Luca Biondi. "Synthesis of Two Novel Mixed Bifunctional Chelating Agents: DO2AP(tBu)4 and DO3AP(tBu)4." Synlett 31, no. 13 (June 16, 2020): 1291–94. http://dx.doi.org/10.1055/s-0040-1707893.

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A convenient synthesis of two novel macrocyclic bifunctional chelating agents (BFCAs), formally derived from the well-known ligands DO3A and DOTA by selective replacement of one carboxymethyl side arm with a phosphonomethyl residue, is reported.

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22

Chen, Na, Shui Wang, Chun Hui Yao, Li Hui, and Yixin Qu. "Solubility ofN-(Phosphonomethyl)iminodiacetic Acid in Different Binary Mixtures." Journal of Chemical & Engineering Data 55, no. 7 (July 8, 2010): 2613–15. http://dx.doi.org/10.1021/je900764f.

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23

Page, Patrick, Marie-Rose Mazières, Jacques Bellan, Michel Sanchez, and Bruno Chaudret. "A SIMPLE AND CONVENIENT SYNTHESIS OF 2-PHOSPHONOMETHYL PYRIDINES." Phosphorus, Sulfur, and Silicon and the Related Elements 70, no. 1 (January 1992): 205–10. http://dx.doi.org/10.1080/10426509208049168.

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24

Juengst, Clifford D., and William P. Weber. "Preparation and properties of dimethyl phosphonomethyl methylsiloxane dimethylsiloxane copolymers." Journal of Polymer Science Part A: Polymer Chemistry 25, no. 7 (July 1987): 1967–78. http://dx.doi.org/10.1002/pola.1987.080250717.

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25

Khoo, Lian Ee, and Alan Hazell. "Polymeric [μ3-(N-phosphonomethyl)glycinato]tris(tri-n-butyltin)." Acta Crystallographica Section C Crystal Structure Communications 57, no. 3 (March 15, 2001): 254–56. http://dx.doi.org/10.1107/s0108270100018898.

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26

Bielecki, Krzysztof, Janusz Sarapuk, and Halina Kleszczynáska. "Binary Mixtures of (N-phosphonomethyl)-glycine with New Aminophosphonates." Zeitschrift für Naturforschung C 59, no. 7-8 (August 1, 2004): 515–18. http://dx.doi.org/10.1515/znc-2004-7-811.

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AbstractThe potential biological activity of binary mixtures of some new organophosphorous compounds, aminoalkane- and aminofluorenephosphonates, with (N-phosphonomethyl)-glycine (glyphosate, PMG) was studied. The inhibition of growth of wheat (Triticum aestivum) induced by individual compounds and their equimolar mixtures with PMG was a measure of that activity. The experiments were expected to show if the new compounds exhibited good biological activity to be used for agrochemical applications and if this activity can be improved when they are used in mixtures with glyphosate which is the active component of the well-known herbicide Roundup. The results obtained show that aminofluorenephosphonates inhibited wheat growth when used in micromolar concentrations. Thus, their efficiency can be compared to that of PMG. The efficiency of aminoalkanephosphonates was one order of magnitude weaker. The measure of the efficiency was the effective concentration inhibiting wheat growth by 50% (EC50). The most demanded interaction, i.e., a synergistic was observed for only one of binary mixtures of the compounds studied with PMG. Mostly they showed antagonistic or strong antagonistic interactions. Some of them were of the additive type. Such results exclude the possibility of potential use of all the compounds studied in binary mixtures with phosphonomethylglycine, especially as the mentioned synergistic interaction found was rather weak. The influence of structural features of aminophosphonates on the results obtained is discussed.

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27

Bischofberger, N., E. R. Kern, M. S. Chen, D. B. Barkhimer, J. M. Cherrington, J. P. Dougherty, C. U. Kim, et al. "Synthesis and antiviral activity of novel phosphonomethyl ether nucleosides." Antiviral Research 26, no. 3 (March 1995): A294. http://dx.doi.org/10.1016/0166-3542(95)94828-p.

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28

Cesnek, Michal, and Piet Herdewijn. "Synthesis and Antiviral Activity of 3-O-Phosphonomethyl Nucleosides." Antiviral Research 86, no. 1 (April 2010): A51. http://dx.doi.org/10.1016/j.antiviral.2010.02.423.

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29

Harizi, Abdallah, and Hedi Zantour. "SYNTHÈSE ET RÉACTIVITÉ DES 2-PHOSPHONOMETHYLBENZIMIDAZOLES N-ETHOXYCARBONYLES: NOUVELLE VOIE D'ACCÈS AUX 2-PHOSPHONOMETHYL N-AMIDOBENZIMIDAZOLES ET AUX 2-PHOSPHONOMETHYL N-HYDRAZIDOBENZIMIDAZOLES." Phosphorus, Sulfur, and Silicon and the Related Elements 162, no. 1 (July 2000): 219–29. http://dx.doi.org/10.1080/10426500008045222.

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30

Feng, Jian-Shen, Zhong-Sheng Cai, Min Ren, Song-Song Bao, and Li-Min Zheng. "Racemic cobalt phosphonates incorporating flexible bis(imidazole) co-ligands." Dalton Transactions 44, no. 41 (2015): 18122–29. http://dx.doi.org/10.1039/c5dt03046c.

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Racemic cobalt phosphonates based on 3-phenyl-3-((phosphonomethyl)amino)propanoic acid (3-ppapH₃) show layered structures composed of Co₃(3-ppap)₂ chains and bis(imidazol-1-ylmethyl)benzene (bix) linkers in trans-modes.

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31

Ioannidis, Panagiotis, Björn Classon, Bertil Samuelsson, Ingemar Kvarnström, Karikath S. Varma, Jan Becher, and Allan E. Underhill. "Synthesis of Some 3',5'-Dideoxy-5'-C-Phosphonomethyl Nucleosides." Acta Chemica Scandinavica 45 (1991): 746–50. http://dx.doi.org/10.3891/acta.chem.scand.45-0746.

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32

Almer, Helena, Björn Classon, Bertil Samuelsson, Ingemar Kvarnström, Karikath S. Varma, Jan Becher, and Allan E. Underhill. "Synthesis of a Phosphonomethyl Analogue of 3'-Deoxy-3'-fluorothymidine." Acta Chemica Scandinavica 45 (1991): 766–67. http://dx.doi.org/10.3891/acta.chem.scand.45-0766.

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33

Bessarabov, Volodymyr, Volodymyr Vasylenko, Lubov Vakhitova, Galina Kuzmina, Nazar Zderko, Viktoriia Plavan, and Glib Zagoriy. "Development of a decontamination system for decomposing N-(phosphonomethyl)glycine." Eastern-European Journal of Enterprise Technologies 3, no. 6 (99) (May 24, 2019): 6–13. http://dx.doi.org/10.15587/1729-4061.2019.168391.

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34

Liu, Yong Bing, En Xiang Liang, Jian Min Yi, Xing Wu, and Pan Liang Zhang. "Preparation of Glyphosate from Catalytic Oxidation N-Phosphonomethyl Iminodiacetic Acid." Applied Mechanics and Materials 556-562 (May 2014): 213–16. http://dx.doi.org/10.4028/www.scientific.net/amm.556-562.213.

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The activated carbon-containing catalysts (Pd/C and Pt/C) have been prepared by surface modification of the activated carbon with palladium chloride and chloroplatinic acid solution, respectively. The Pt/C catalyst is characterized by XRD pattern. The glyphosate is prepared from catalytic oxidation N-phosphonomethyl iminodiacetic acid. Effect of different catalysts and amount of the catalyst in catalytic oxidation are investigated. Compared with Pt/C catalyst, Pd/C catalyst is more active. Optimum amount of Pd/C catalyst is 45 mol/m3 PMIDA.

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35

Smith, Paul H., and Kenneth N. Raymond. "Solid-state and solution chemistry of calcium N-(phosphonomethyl)glycinate." Inorganic Chemistry 27, no. 6 (March 1988): 1056–61. http://dx.doi.org/10.1021/ic00279a024.

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36

Abdelli, Abderrahmen, Mohamed Lotfi Efrit, Anne Gaucher, Hedi M’rabet, and Damien Prim. "A convenient synthesis of phosphonomethyl α,β-unsaturated γ-lactams." Tetrahedron Letters 56, no. 40 (September 2015): 5397–400. http://dx.doi.org/10.1016/j.tetlet.2015.07.088.

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37

Ruiz, María, Vicente Ojea, Susana Conde, and José M. Quintela. "Diastereoselective Synthesisof 3-Phosphonomethyl-substituted Cyclohexyl- and Cyclohex-2-enylglycines." Synlett, no. 5 (2003): 0689–93. http://dx.doi.org/10.1055/s-2003-38348.

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38

Brokeš, J., and A. Holý. "Synthesis of 5'-O-phosphonomethyl derivatives of biologically active nucleosides." Collection of Czechoslovak Chemical Communications 55, s1 (1990): 125–28. http://dx.doi.org/10.1135/cccc1990s125.

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39

Maier, Ludwig, and Tammo Winkler. "ORGANIC PHOSPHORUS COMPOUNDS 99.1SYNTHESIS AND PROPERTIES OF N-PHOSPHONOMETHYL-AMINOACETALDEHYDE." Phosphorus, Sulfur, and Silicon and the Related Elements 63, no. 1-2 (November 1991): 65–69. http://dx.doi.org/10.1080/10426509108029428.

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40

Harsányi, Kálmán, György Domány, István Greiner, Henrietta Forintos, and György Keglevich. "Synthesis of 2-phosphinoxidomethyl- and 2-phosphonomethyl glutaric acid derivatives." Heteroatom Chemistry 16, no. 7 (2005): 562–65. http://dx.doi.org/10.1002/hc.20142.

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41

Naydenova, Emilia D., Petar T. Todorov, Margarita N. Topashka-Ancheva, Georgi Ts Momekov, Tsvetelina Z. Yordanova, Spiro M. Konstantinov, and Kolio D. Troev. "Novel N-(phosphonomethyl) glycine derivatives: Design, characterization and biological activity." European Journal of Medicinal Chemistry 43, no. 6 (June 2008): 1199–205. http://dx.doi.org/10.1016/j.ejmech.2007.08.010.

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42

Lee, Shi Yong. "Preparation, Alkylation, and Olefination Reaction of 5-Phosphonomethyl-3-methylisoxazole." Synthesis 1999, no. 12 (December 1999): 2027–29. http://dx.doi.org/10.1055/s-1999-3625.

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43

Zhu, Hui, Jian Huang, Song-Song Bao, Min Ren, and Li-Min Zheng. "Racemic metal phosphonates based on 1-phosphonomethyl-2-benzimidazol-piperidine." CrystEngComm 15, no. 47 (2013): 10316. http://dx.doi.org/10.1039/c3ce41642a.

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44

Niklasson, Annika, Ingemar Kvarnström, Björn Classon, and Bertil Samuelsson. "Synthesis of 2•,3•-Dideoxy-3•-C-hydroxymethylcytidine Phosphonomethyl Derivatives." Molecules Online 2, no. 1 (January 8, 1998): 7–14. http://dx.doi.org/10.1007/s007830050048.

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45

Feng, Jian-Shen, Min Ren, Zhong-Sheng Cai, Kun Fan, Song-Song Bao, and Li-Min Zheng. "Enantiopure phosphonic acids as chiral inducers: homochiral crystallization of cobalt coordination polymers showing field-induced slow magnetization relaxation." Chemical Communications 52, no. 42 (2016): 6877–80. http://dx.doi.org/10.1039/c6cc02463g.

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Homochiral crystallization of (M)- or (P)-Co(SO₄)(1,3-bbix)(H₂O)₃ (1M or 1P) from an achiral precursor is achieved in the presence of a catalytic amount of (S)- or (R)-3-phenyl-2-((phosphonomethyl)amino) propanoic acid.

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46

Herdewijn, Piet, and Michal Cesnek. "Synthesis and Anti-HIV Activity of New 3’-O-Phosphonomethyl Nucleosides." HETEROCYCLES 82, no. 1 (2010): 663. http://dx.doi.org/10.3987/com-10-s(e)42.

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47

Paudel, Rishi R., Jeremy N. Ridenour, Nigam P. Rath, and Christopher D. Spilling. "Synthesis of Phosphonomethyl Tetrahydrofurans via the Mori–Tamaru Reaction of Phosphonodienes." Organic Letters 22, no. 10 (April 24, 2020): 3830–34. http://dx.doi.org/10.1021/acs.orglett.0c01080.

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48

Bo, Liu, and Zhan Jiarong. "An Efficient Synthesis of Nα-Fmocm-(phosphonomethyl)-L- and D-Phenylalanine." Synthetic Communications 29, no. 13 (July 1999): 2293–99. http://dx.doi.org/10.1080/00397919908086231.

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49

Page, Patrick, Casimir Blonski, and Jacques Périé. "Interaction of phosphonomethyl analog of dihydroxyacetone phosphate with rabbit muscle aldolase." Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology 1386, no. 1 (July 1998): 59–64. http://dx.doi.org/10.1016/s0167-4838(98)00061-2.

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50

Viña, Dolores, Tongfei Wu, Marleen Renders, Geneviève Laflamme, and Piet Herdewijn. "Synthesis of 3′-O-phosphonomethyl nucleosides with an adenine base moiety." Tetrahedron 63, no. 12 (March 2007): 2634–46. http://dx.doi.org/10.1016/j.tet.2007.01.032.

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