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Artykuły w czasopismach na temat „Bis-phosphonic acids”

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Data publikacji: 11 lipca 2023

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1

Rao, B. Venkateswara, and D. M. Puri. "Copper(II) Complexes of Organophoshonic Acids-A Comparative Study." E-Journal of Chemistry 8, s1 (2011): S271—S281. http://dx.doi.org/10.1155/2011/813586.

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Polynuclear copper(II) derivatives of 1-hydroxyethylidenediphosphonic acid (HEDP), 1-aminoethylidenediphosphonic acid (AEDP, H4L),α-aminobenzylidene diphosphonic acid (ABDP, H4L), 1-amino-2-carboxyethane- 1,1-diphosphonic acid (ACEDP, H5L), 1,3 diaminopropane-1,1,3,3-tetra-phosphonic acid (DAPTP, H8L), Ethylenediamine-N,N'-bis (dimethyl-methylenephosphonic) acid (EDBDMPO, H4L),o-phenylene-diamine-N,N'-bis (dimethylmethylenephosphonic) acid (PDBDMPO, H4L), diethylene triamine –N,N,N',N',N"N-penta (methylene phosphonic) acid (DETAPMPO, H10L) and diethylene triamine –N,N"-bis (dimethyl methylene

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2

Popov, Konstantin, Hannu Rönkkömäki, and Lauri H. J. Lajunen. "Critical evaluation of stability constants of phosphonic acids (IUPAC Technical Report)." Pure and Applied Chemistry 73, no. 10 (2001): 1641–77. http://dx.doi.org/10.1351/pac200173101641.

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Available experimental data on stability constants of proton and metal complexes for 10 phosphonic acids [methylphosphonic acid, 1-hydroxyethane-1,1-diylbisphosphonic acid, dichloromethylenebisphosphonic acid, amino-methanephosphonic acid, N-(phosphonomethyl)glycine, imino-N,N-bis(methylenephosphonic acid), N-methylamino-N,N-bis(methylenephosphonic acid), nitrilotris(methylenephosphonic acid), 1,2-diaminoethane-N,N,N´,N´-tetrakis-(methylenephosphonic acid), and diethylenetriamine-N,N,N´,N´´,N´´-pentakis-(methylenephosphonic acid)], published in 19501997, have been critically evaluated. For th

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3

Chung, Yeong-Jin. "Combustive Characteristics of Wood Specimens Treated with Alkylenediaminoalkyl-Bis-Phosphonic Acids." Journal of Korean Institute of Fire Science and Engineering 27, no. 6 (2013): 57–63. http://dx.doi.org/10.7731/kifse.2013.27.6.057.

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4

Penicaud, Virginie, Fabrice Odobel, and Bruno Bujoli. "Facile and efficient syntheses of 2,2′-bipyridine-based bis(phosphonic) acids." Tetrahedron Letters 39, no. 22 (1998): 3689–92. http://dx.doi.org/10.1016/s0040-4039(98)00647-9.

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5

Yushkova, Yu V., S. V. Morozov, E. I. Chernyak, and N. A. Grigor′ev. "Synthesis of New Trolox-Based Antioxidants Containing Amino-bis-Phosphonic Acids." Chemistry of Natural Compounds 53, no. 4 (2017): 764–66. http://dx.doi.org/10.1007/s10600-017-2115-z.

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6

Guenin, Erwann, Estelle Degache, Jean Liquier, and Marc Lecouvey. "Synthesis of 1-Hydroxymethylene-1,1-bis(phosphonic acids) from Acid Anhydrides: Preparation of a New Cyclic 1-Acyloxymethylene-1,1-bis(phosphonic acid)." European Journal of Organic Chemistry 2004, no. 14 (2004): 2983–87. http://dx.doi.org/10.1002/ejoc.200400053.

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7

Kalchenko, Vitaly, Olga Kalchenko, and Sergiy Cherenok. "Complexation of Calix[4]arene bis-Hydroxymethylenediphosphonic Acid with Amino acids. Binding Constants Determination by RP HPLC Method." French-Ukrainian Journal of Chemistry 3, no. 2 (2015): 93–100. http://dx.doi.org/10.17721/fujcv3i2p93-100.

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Host-Guest complexation of calixarene-bis-hydroxymethylenediphosphonic acid with 17 amino acids in water solution had been studied by the RP HPLC and molecular modelling methods. It had been shown the binding constants of the complexes are depended on the nature of the amino acid residue, log P and pKa of the acids. The complexation is mainly determined by the electrostatic interactions between the positively charged nitrogen atom of the amino acid and the negatively charged oxygen atom of phosphonic acid residue of the calixarene, the Host-Guest p-p, СН-p and solvophobic interactions.

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8

Vrbovská, Silvie, Antonín Holý, Radek Pohl, and Milena Masojídková. "Bifunctional Acyclic Nucleoside Phosphonates. 1. Symmetrical 1,3-Bis[(phosphonomethoxy)propan-2-yl] Derivatives of Purines and Pyrimidines." Collection of Czechoslovak Chemical Communications 71, no. 4 (2006): 543–66. http://dx.doi.org/10.1135/cccc20060543.

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We report here a general method for the synthesis of new symmetrical bis-phosphonates of acyclic nucleosides. 1,3-Bis[(diisopropoxyphosphoryl)methoxy] derivatives of purine and pyrimidine bases were prepared by their reaction with 1,3-bis[(diisopropoxyphosphoryl)-methoxy]propan-2-yl tosylate. Cytosine, uracil and thymine provided regiospecificallyN1-isomers. This alkylation regiospecificity applies to several other tosylates of primary and secondary alcohols as well. 6-Chloropurine and 2-amino-6-chloropurine were alkylated in N9position. Resulting bis-phosphonates were converted to the respect

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9

Pirat, J. L., C. Brahic, C. Ciptadi, H. J. Cristau, A. Hervé, and D. Virieux. "Bis(hydroxymethyl)phosphine Oxides and Hydroxymethyl Phosphinic Acids as Phosphonic Acid Analogs." Phosphorus, Sulfur, and Silicon and the Related Elements 177, no. 8-9 (2002): 2221–22. http://dx.doi.org/10.1080/10426500213342.

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10

Justyna, Katarzyna, Joanna Małolepsza, Damian Kusy, Waldemar Maniukiewicz, and Katarzyna M. Błażewska. "The McKenna reaction – avoiding side reactions in phosphonate deprotection." Beilstein Journal of Organic Chemistry 16 (June 23, 2020): 1436–46. http://dx.doi.org/10.3762/bjoc.16.119.

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The McKenna reaction is a well-known and popular method for the efficient and mild synthesis of organophosphorus acids. Bromotrimethylsilane (BTMS) is the main reagent in this reaction, which transforms dialkyl phosphonate esters into bis(trimethylsilyl)esters, which are then easily converted into the target acids. However, the versatile character of the McKenna reaction is not always used to its full extent, due to formation of side products. Herein, demonstrated by using model examples we have not only analyzed the typical side processes accompanying the McKenna reaction, but also uncovered

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11

Dvořáková, Hana, Antonín Holý, and Petr Alexander. "Synthesis and Biological Effects of 9-(3-Hydroxy-2-phosphonomethoxypropyl) Derivatives of Deazapurine Bases." Collection of Czechoslovak Chemical Communications 58, no. 6 (1993): 1403–18. http://dx.doi.org/10.1135/cccc19931403.

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Analogs of antiviral 9-(S)-(3-hydroxy-2-phosphonomethoxypropyl)adenine (HPMPA, I), containing modified purine bases 3-deazaadenine XII, 1-deazaadenine XIV, 7-deaz-7-cyanoaadenine XXXII and 3-deazaguanine XXXVIII, were prepared by alkylation of the bases with synthon XVII, containing preformed structure of the side chain, in the presence of cesium carbonate. The obtained protected derivatives were deblocked successively with sodium methoxide and bromotrimethylsilane to give phosphonic acids XII, XIV, XXXII and XXXVIII. Compounds XII, XIV and XVI were also prepared from (S)- or (R)-9-(2,3-dihydr

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12

Park, Myung-Ho, and Yeong-Jin Chung. "Combustion Characteristics of Medium Density Fibreboard (MDF) Painted with Alkylenediaminoalkyl-Bis-Phosphonic Acids." Applied Chemistry for Engineering 25, no. 5 (2014): 481–86. http://dx.doi.org/10.14478/ace.2014.1066.

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13

Nasulewicz‐Goldeman, Anna, Waldemar Goldeman, Ewa Mrówczyńska, and Joanna Wietrzyk. "Biological effects of aromatic bis[aminomethylidenebis(phosphonic)] acids in osteoclast precursors in vitro." Chemical Biology & Drug Design 94, no. 4 (2019): 1835–48. http://dx.doi.org/10.1111/cbdd.13597.

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14

PENICAUD, V., F. ODOBEL, and B. BUJOLI. "ChemInform Abstract: Facile and Efficient Syntheses of 2,2′-Bipyridine-Based Bis(phosphonic) Acids." ChemInform 29, no. 35 (2010): no. http://dx.doi.org/10.1002/chin.199835214.

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15

Dvořáková, Hana, and Antonín Holý. "Synthesis and Biological Effects of N-(2-Phosphonomethoxyethyl) Derivatives of Deazapurine Bases." Collection of Czechoslovak Chemical Communications 58, no. 6 (1993): 1419–29. http://dx.doi.org/10.1135/cccc19931419.

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Analogs of antiviral 9-(2-phosphonomethoxyethyl)adenine (PMEA,II), containing modified purine bases 1-deazaadenine (VII, 3-deazapurine (XI), 7-deaza-7-cyanoadenine (XIIIb) and 3-deazaguanine (XXIb) were prepared by alkylation of the heterocyclic bases with bis(2-propyl) 2-chloroethoxymethylphosphonate (V) in dimethylformamide in the presence of sodium hydride or cesium carbonate. The obtained protected derivatives were deblocked with bromotrimethylsilane to give the phosphonic acids. 3-DeazaPMEG (XXIb) is active against DNA viruses and exhibits a marked cytostatic effect against L-1210 leukemi

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16

Alferiev, Ivan S., and Sergey Yu Bobkov. "Cyclic Oligophosphonic Anhydrides Stable in Aqueous Media." Zeitschrift für Naturforschung B 47, no. 9 (1992): 1213–24. http://dx.doi.org/10.1515/znb-1992-0902.

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Depending on reaction conditions, the phosphonylation of N-alkylacetamides with H3PO3– PCl3 in B · HCl media (B = Py, Bu3N) gives either 1-alkylaminoethylidene-1,1-bisphosphonic acids (la–e) or previously unknown 1-alkylaminobutane-1,1,3,3-tetrayl-tetrakisphosphonic dianhydrides (2a–e). The latter convert into monocyclic forms (3a–e) under mild acidic hydrolysis. Acyclic forms (4a–e) cannot be isolated. In the presence of higher N,N-dialkylamides the phosphonylation of acetamides affords the higher dianhydrides (2f–h). Strong acidic hydrolysis of 2 or 3 yields 3,3-diphosphonocarboxylic acids (

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17

Park, Myung-Ho, and Yeong-Jin Chung. "Combustive Properties of Medium Density Fibreboards (MDF) Treated with Bis-(Dimethylaminomethyl) Phosphinic Acid and Alkylenediaminoalkyl-Bis-Phosphonic Acids." Fire Science and Engineering 28, no. 5 (2014): 71–79. http://dx.doi.org/10.7731/kifse.2014.28.5.071.

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18

Prishchenko, Andrey A., Mikhail V. Livantsov, Olga P. Novikova, Ludmila I. Livantsova, and Valery S. Petrosyan. "Synthesis of new five-membered N-heterocycle derivatives of mono- and bis-phosphonic acids." Mendeleev Communications 27, no. 1 (2017): 90–92. http://dx.doi.org/10.1016/j.mencom.2017.01.029.

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19

Baulin, V. E., G. S. Tsebrikova, D. V. Baulin, and Y. F. Al Ansary. "1,5-bis[2-(dioxyphosphoryl)-4-ethylphenoxy]-3-oxapentane and its Analogs as Promising Organic Ligands for Copper(II) Binding s." Biomedical Chemistry: Research and Methods 1, no. 3 (2018): e00043. http://dx.doi.org/10.18097/bmcrm00043.

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The dissociation and complexation ability toward Cu(II) of acidic type phosphoryl-containing podands – tetrabasic 1,5-bis[2-(dioxyphosphoryl)-4-ethylphenoxy]-3-oxapentane (L1), dibasic – 1,5-bis[2-(ethoxyhydroxyphosphoryl)-4-ethylphenoxy]-pentane (L2) and also of their carboxylic analogue dibasic 1,5-bis[2-(oxycarbonylphenoxy)]-3-oxapentane (L3) were investigated by spectrophotometric, conductometric and potentiometric methods in water in the presence 5% of dimethyl formamide. Spectrophotometric and conductometric titration data provided evidence for formation of 1:1 (M:L) complexes. The disso

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20

Nasulewicz-Goldeman, Anna, Waldemar Goldeman, Anna Nikodem, et al. "Aromatic Bis[aminomethylidenebis(phosphonic)] Acids Prevent Ovariectomy-Induced Bone Loss and Suppress Osteoclastogenesis in Mice." International Journal of Molecular Sciences 22, no. 17 (2021): 9590. http://dx.doi.org/10.3390/ijms22179590.

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Osteoporosis is a skeletal disease associated with excessive bone turnover. Among the compounds with antiresorptive activity, nitrogen-containing bisphosphonates play the most important role in antiosteoporotic treatment. In previous studies, we obtained two aminomethylidenebisphosphonates—benzene-1,4-bis[aminomethylidene(bisphosphonic)] (WG12399C) acid and naphthalene-1,5-bis[aminomethylidene(bisphosphonic)] (WG12592A) acid—which showed a significant antiproliferative activity toward J774E macrophages, a model of osteoclast precursors. The aim of these studies was to evaluate the antiresorpti

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21

Alter, Christian, Beate Neumann, Hans-Georg Stammler, and Berthold Hoge. "Bis(diethylamino)pentafluorophenylphosphane as Valuable Precursor for the Design of Tetrafluorophenylphosphanes, Tetrafluorophenylphosphinic and -phosphonic Acids." European Journal of Inorganic Chemistry 2018, no. 7 (2018): 867–75. http://dx.doi.org/10.1002/ejic.201701402.

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22

Classen, R., and G. Hagele. "A novel method for the preparation of fluoroaryl- and fluoroalkyl-substituted bis- and tris-phosphonic acids." Journal of Fluorine Chemistry 77, no. 1 (1996): 71–81. http://dx.doi.org/10.1016/0022-1139(95)03387-4.

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23

Egorov, Maxim, Sameh Aoun, Marc Padrines, et al. "A One-Pot Synthesis of 1-Hydroxy-1,1-bis(phosphonic acid)s Starting from the Corresponding Carboxylic Acids." European Journal of Organic Chemistry 2011, no. 35 (2011): 7148–54. http://dx.doi.org/10.1002/ejoc.201101094.

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24

Lewkowski, Jarosław, and Marek Dziȩgielewski. "Addition of di-(trimethylsilyl)phosphite toN,N′-dialkyl terephthalic schiff bases: Synthesis of 1,4-phenylene-bis- (aminomethyl)-phosphonic acids." Heteroatom Chemistry 20, no. 7 (2009): 431–35. http://dx.doi.org/10.1002/hc.20569.

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25

Das, Swagatika, Umashankar Das, Hiroshi Sakagami, et al. "Sequential cytotoxicity: A theory examined using a series of 3,5-bis(benzylidene)-1-diethylphosphono-4-oxopiperidines and related phosphonic acids." Bioorganic & Medicinal Chemistry Letters 20, no. 22 (2010): 6464–68. http://dx.doi.org/10.1016/j.bmcl.2010.09.051.

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Egorov, Maxim, Sameh Aoun, Marc Padrines, et al. "ChemInform Abstract: A One-Pot Synthesis of 1-Hydroxy-1,1-bis(phosphonic acid)s Starting from the Corresponding Carboxylic Acids." ChemInform 43, no. 19 (2012): no. http://dx.doi.org/10.1002/chin.201219193.

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27

Ouksel, Louiza, Riadh Bourzami, Salah Chafaa, and Nadjib Chafai. "Solvent and catalyst-free synthesis, corrosion protection, thermodynamic, MDS and DFT calculation of two environmentally friendly inhibitors: Bis-phosphonic acids." Journal of Molecular Structure 1222 (December 2020): 128813. http://dx.doi.org/10.1016/j.molstruc.2020.128813.

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28

Venkatramaiah, Nutalapati, Ricardo F. Mendes, Artur M. S. Silva, João P. C. Tomé, and Filipe A. Almeida Paz. "A ladder coordination polymer based on Ca2+and (4,5-dicyano-1,2-phenylene)bis(phosphonic acid): crystal structure and solution-state NMR study." Acta Crystallographica Section C Structural Chemistry 72, no. 9 (2016): 685–91. http://dx.doi.org/10.1107/s2053229616012328.

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The preparation of coordination polymers (CPs) based on either transition metal centres or rare-earth cations has grown considerably in recent decades. The different coordination chemistry of these metals allied to the use of a large variety of organic linkers has led to an amazing structural diversity. Most of these compounds are based on carboxylic acids or nitrogen-containing ligands. More recently, a wide range of molecules containing phosphonic acid groups have been reported. For the particular case of Ca2+-based CPs, some interesting functional materials have been reported. A novel one-d

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29

Lewkowski, Jaroslaw, and Marek Dziegielewski. "ChemInform Abstract: Addition of Di-(trimethylsilyl)phosphite to N,N′-Dialkyl Terephthalic Schiff Bases: Synthesis of 1,4-Phenylene-bis-(aminomethyl)-phosphonic Acids." ChemInform 41, no. 23 (2010): no. http://dx.doi.org/10.1002/chin.201023166.

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30

Maruk, Alesya Ya, Valery V. Ragulin, Iurii A. Mitrofanov, et al. "Synthesis, Complexation Properties, and Evaluation of New Aminodiphosphonic Acids as Vector Molecules for 68Ga Radiopharmaceuticals." Molecules 26, no. 8 (2021): 2357. http://dx.doi.org/10.3390/molecules26082357.

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Two new aminodiphosphonic acids derived from salicylic acid and its phosphonic analogue were prepared through a simple and efficient synthesis. 2-[(2-Amino-2,2-diphosphono)ethyloxy]-benzoic acid 8 and 2-[(2-amino-2,2-diphosphono)ethyloxy]-5-ethyl-phenylphosphonic acid 9 were evaluated for their applicability as 68Ga binding bone-seeking agents. Protonation constants of 8 and 9 and stability constants of the Ga3+ complexes with 8 and 9 in water were determined. The stability constant of Ga3+ complex with fully phosphorylated acid 9 (logKGaL = 31.92 ± 0.32) significantly exceeds stability consta

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31

Penicaud, V., D. Massiot, G. Gelbard, F. Odobel, and B. Bujoli. "Preparation of structural analogues of divalent metal monophosphonates, using bis(phosphonic) acids: a new strategy to reduce overcrowding of organic groups in the interlayer space." Journal of Molecular Structure 470, no. 1-2 (1998): 31–38. http://dx.doi.org/10.1016/s0022-2860(98)00467-0.

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Sowa, Michał, Katarzyna Ślepokura, Waldemar Goldeman, Marek Duczmal, Agnieszka Wojciechowska, and Ewa Matczak-Jon. "Structural characterization of pyridin-2-, -3-, and -4-yl functionalized (iminodimethanediyl)bis(phosphonic) acids: Insight into the cobalt(II) and copper(II) complexes of pyridin-2-yl derivative." Polyhedron 50, no. 1 (2013): 398–409. http://dx.doi.org/10.1016/j.poly.2012.11.023.

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Neuman, A., M. Coindet-Benramdane, H. Gillier, Y. Leroux, D. El Manouni, and T. Prangé. "Crystal structure of (1-hydroxy-l-phosphono-pentyl)-phosphonic acid dimethyl ammonium salt, C7H21NO7P2, and of (1,8-dihydroxy-1,8,8-trisphosphono- octyl)-phosphonic acid bis-dimethylammonium salt tetrahydrate, C12H36N2O14P4 · 4H2O, evidence for trapped alcaline species by bisphosphonic and tetraphosphonic acids in the crystalline state." Zeitschrift für Kristallographie - New Crystal Structures 217, JG (2002): 154–56. http://dx.doi.org/10.1524/ncrs.2002.217.jg.154.

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Neuman, A., M. Coindet-Benramdane, H. Gillier, Y. Leroux, D. El Manouni, and T. Prangé. "Crystal structure of (1-hydroxy-l-phosphono-pentyl)-phosphonic acid dimethyl ammonium salt, C7H21NO7P2, and of (1,8-dihydroxy-1,8,8-trisphosphono- octyl)-phosphonic acid bis-dimethylammonium salt tetrahydrate, C12H36N2O14P4 · 4H2O, evidence for trapped alcaline species by bisphosphonic and tetraphosphonic acids in the crystalline state." Zeitschrift für Kristallographie - New Crystal Structures 217, no. 1 (2002): 154–56. http://dx.doi.org/10.1524/ncrs.2002.217.1.154.

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Guenin, Erwann, Estelle Degache, Jean Liquier, and Marc Lecouvey. "Synthesis of 1-Hydroxymethylene-1,1-bis(phosphonic acids) from Acid Anhydrides: Preparation of a New Cyclic 1-Acyloxymethylene-1,1-bis(phosphonic acid)." ChemInform 35, no. 44 (2004). http://dx.doi.org/10.1002/chin.200444194.

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Kalchenko, O. I., S. O. Cherenok, O. M. Silenko, and V. I. Kalchenko. "Influence of the Nature of Amino Acids on the Formation of Supramolecular Complexes with Calixarenemethylene-bis-Phosphonic Acid." Theoretical and Experimental Chemistry, December 14, 2022. http://dx.doi.org/10.1007/s11237-022-09742-5.

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