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Journal articles on the topic 'Phosphorus halides'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Al-Hemyari, Abdullah, Areej Hashim, Muna Bufaroosha, and Thies Thiemann. "Use of Triphenylphosphine-Bromotrichloromethane (PPh3-BrCCl3) in the Preparation of Acylhydrazines, N-Methylamides, Anilides and N-Arylmaleimides From Carboxylic Acids." Proceedings 41, no. 1 (November 14, 2019): 4. http://dx.doi.org/10.3390/ecsoc-23-06460.

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In certain countries, many of the reagents used to transform carboxylic acids to acyl halides such as phosphorus trichloride, phosphorus tribromide, phosphorus pentachloride, phosphoryl chloride, thionyl chloride and sulfuryl chloride are difficult to come by. Against this background, the authors developed the reaction system triphenylphosphine (PPh3)–bromotrichloromethane (BrCCl3) to prepare acyl halides in situ. In the following, the use of this reagent combination is joined with the reaction of the in situ prepared acyl halides with nitrogen nucleophiles, specifically with hydrazines, methylamine and anilines. The reaction is also used in an intramolecular variant by the reaction of maleanilic acids to N-arylmaleimides.

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2

Blachnik, Roger, Kerstin Hackmann, and Hans-Peter Baldus. "Neue Phosphorchalkogenahalogenide / New Phosphorus Chalcogena Halides." Zeitschrift für Naturforschung B 46, no. 9 (September 1, 1991): 1165–68. http://dx.doi.org/10.1515/znb-1991-0905.

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α-P4Se3Br2 and α-P4Se3CL2 were prepared from α-P4Se3I2 by reaction with silver bromide resp. silver chloride in CS2-solution. Using bismuth or mercury halides it was also possible to obtain β-P4X3Br2 and β-P4X3Cl2 from β-P4X3I2 (X = S, Se). The 31P NMR data of these compounds are given.

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3

Narain, R. P., and Mahtab Z. Siddiqui. "Reactions of phosphorus halides with urethane." Polyhedron 4, no. 3 (January 1985): 467–70. http://dx.doi.org/10.1016/s0277-5387(00)87011-4.

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4

Tattershall, Bruce W., and Nigel L. Kendall. "NMR evidence for new phosphorus halides." Polyhedron 13, no. 10 (May 1994): 1517–21. http://dx.doi.org/10.1016/s0277-5387(00)83446-4.

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5

BLACHNIK, R., K. HACKMANN, and H. P. BALDUS. "ChemInform Abstract: New Phosphorus Chalcogen Halides." ChemInform 22, no. 49 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199149031.

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6

Huangfu, Xinlei, Yue Zhang, Peiyun Chen, Guozhang Lu, Yinwei Cao, Guo Tang, and Yufen Zhao. "Synthesis of mixed phosphorotrithioates from white phosphorus." Green Chemistry 22, no. 23 (2020): 8353–59. http://dx.doi.org/10.1039/d0gc02985h.

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7

Petko, Dina, Samuel Koh, and William Tam. "Transition Metal-Catalyzed Reactions of Alkynyl Halides." Current Organic Synthesis 16, no. 4 (July 4, 2019): 546–82. http://dx.doi.org/10.2174/1570179416666190329200616.

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Background: Transition metal-catalyzed reactions of alkynyl halides are a versatile means of synthesizing a wide array of products. Their use is of particular interest in cycloaddition reactions and in constructing new carbon-carbon and carbon-heteroatom bonds. Transition metal-catalyzed reactions of alkynyl halides have successfully been used in [4+2], [2+2], [2+2+2] and [3+2] cycloaddition reactions. Many carbon-carbon coupling reactions take advantage of metal-catalyzed reactions of alkynyl halides, including Cadiot-Chodkiewicz, Suzuki-Miyaura, Stille, Kumada-Corriu and Inverse Sonogashira reactions. All the methods of constructing carbon-nitrogen, carbon-oxygen, carbon-phosphorus, carbon-sulfur, carbon-silicon, carbon-selenium and carbon-tellurium bonds employed alkynyl halides. Objective: The purpose of this review is to highlight and summarize research conducted in transition metalcatalyzed reactions of alkynyl halides in recent years. The focus will be placed on cycloaddition and coupling reactions, and their scope and applicability to the synthesis of biologically important and industrially relevant compounds will be discussed. Conclusion: It can be seen from the review that the work done on this topic has employed the use of many different transition metal catalysts to perform various cycloadditions, cyclizations, and couplings using alkynyl halides. The reactions involving alkynyl halides were efficient in generating both carbon-carbon and carbonheteroatom bonds. Proposed mechanisms were included to support the understanding of such reactions. Many of these reactions face retention of the halide moiety, allowing additional functionalization of the products, with some new products being inaccessible using their standard alkyne counterparts.

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8

Malysheva, Svetlana, Boris Sukhov, Nina Gusarova, Svetlana Shaikhudinova, Tat'yana Kazantseva, Natal'ya Belogorlova, Vladimir Kuimov, and Boris Trofimov. "Phosphorylation of Allyl Halides with White Phosphorus." Phosphorus, Sulfur, and Silicon and the Related Elements 178, no. 3 (March 1, 2003): 425–29. http://dx.doi.org/10.1080/10426500307917.

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9

KOLODYAZHNYI, O. I. "ChemInform Abstract: P-Halides of Phosphorus Ylides." ChemInform 22, no. 34 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199134291.

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10

Panferova, Liubov I., Vitalij V. Levin, Marina I. Struchkova, and Alexander D. Dilman. "Light-mediated copper-catalyzed phosphorus/halogen exchange in 1,1-difluoroalkylphosphonium salts." Chemical Communications 55, no. 9 (2019): 1314–17. http://dx.doi.org/10.1039/c8cc09115c.

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11

Peringer, Paul, and Peter-Paul Winkler. "Ring opening reactions of tetrahydrofurane with phosphorus halides." Inorganica Chimica Acta 118, no. 1 (August 1986): L1—L2. http://dx.doi.org/10.1016/s0020-1693(00)86389-6.

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12

TATTERSHALL, B. W., and N. L. KENDALL. "ChemInform Abstract: NMR Evidence for New Phosphorus Halides." ChemInform 25, no. 44 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199444014.

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13

Pinchuk, Alexander M., Andrew A. Tolmachev, Alexander N. Kostyuk, Alexander A. Yurchenko, and Angelika I. Sviridon. "C-Phosphorylation of Azoles with Trivalent Phosphorus Halides." Phosphorus, Sulfur, and Silicon and the Related Elements 109, no. 1-4 (January 1996): 477–80. http://dx.doi.org/10.1080/10426509608545194.

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14

Volynskii, N. P., and L. I. Perepelitchenko. "Cleavage of ethers and esters by phosphorus halides." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 35, no. 4 (April 1986): 779–84. http://dx.doi.org/10.1007/bf00954229.

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15

Abdreimova, R. R., F. Kh Faizova, and A. A. Karimova. "Copper (II) Mediated Oxidative Alkoxylation of White Phosphorus. Communication 1." Eurasian Chemico-Technological Journal 12, no. 3,4 (May 19, 2010): 259. http://dx.doi.org/10.18321/ectj53.

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White phosphorus has been oxidized by copper (II) acetylacetonate, halides or carboxylates in aliphatic alcohols to yield dialkyl phosphates and trialkyl phosphates under inert atmosphere and mild reaction conditions. Trialkyl phosphite has been observed as unstable organophosphorus intermediate, which is being converted into the main reaction products. In the case of methanolic solutions, the derivatives of two step acidolysis of dimethyl phosphite, monomethyl phosphite and phosphorous acid, have been additionally detected among the reaction products. The influence of the copper (II) oxidants on the kinetics of accumulation and transmutation of organophosphorus products has been explored. The order of oxidative ability of the copper (II) compounds has been established. The major steps of the reaction including (i) the coordination of white phosphorus and alcohol to metal ion and (ii) the redox decomposition of this intermediate complex accompanied by reducing elimination of elementary copper and formation of organophosphorus product have been also suggested.

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16

Abdreimova, R. R., F. Kh Faizova, and A. A. Karimova. "Copper (II) Catalyzed Oxidative Alkoxylation of White Phosphorus. Communication 2." Eurasian Chemico-Technological Journal 12, no. 3,4 (May 19, 2010): 267. http://dx.doi.org/10.18321/ectj54.

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White phosphorus has been catalytically oxidized by oxygen in alcoholic solutions of copper (II) acetylacetonate, halides or carboxylates to yield dialkyl phosphites and trialkyl phosphates under mild reaction conditions. Trialkyl phosphite has been observed as unstable organophosphorus intermediate, which is being converted into the main reaction products. In the case of methanolic solutions, the derivatives of two step acidolysis of dimethyl phosphite, monomethyl phosphite and phosphorous acid, have been additionally detected among the reaction products. The influence of the copper (II) catalysts on the kinetics of accumulation and transmutation of organophosphorus products has been explored. It has been found that the Cu(II) compounds take a role of catalysts-electron-carriers from white phosphorus to oxygen. The indispensable molar ratio between catalyst and white phosphorus and the order of catalytic activity for the copper (II) compounds have been established. The major steps of the catalytic reaction including (i) the coordination of white phosphorus and alcohol to metal ion, (ii) the redox decomposition of this intermediate complex accompanied by reducing elimination of elementary copper and formation of organophosphorus product and (iii) the oxidation of the reduced form of catalyst by oxygen have been<br />also suggested.

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17

Ouryupin, Andrei B., Ivan A. Rakhov, and Tatyana A. Mastryukova. "Reactions of phosphorus acid halides withN-silylated organic compounds." Russian Chemical Reviews 67, no. 9 (September 30, 1998): 749–59. http://dx.doi.org/10.1070/rc1998v067n09abeh000432.

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18

Bezgubenko, L. V., S. E. Pipko, and A. D. Sinitsa. "Phosphorus halides complexes with 4-dimethylaminopyridine and N-methylimidazole." Russian Journal of General Chemistry 79, no. 5 (May 2009): 911–18. http://dx.doi.org/10.1134/s1070363209050089.

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19

Novak, Igor. "MOLECULAR AND ELECTRONIC STRUCTURE OF LESS COMMON PHOSPHORUS HALIDES." Phosphorus, Sulfur, and Silicon and the Related Elements 68, no. 1-4 (May 1992): 15–23. http://dx.doi.org/10.1080/10426509208038367.

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20

Zykova, A. "Synthesis and Structure of Aryl Phosphorus Compounds." Bulletin of the South Ural State University series "Chemistry" 12, no. 4 (2020): 5–50. http://dx.doi.org/10.14529/chem200401.

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Based on an analysis of the literature published from the late 20th century to the beginning of the 21st century, methods for the synthesis of some complex tetraorganylphosphonium salts are systematized and described, along with the features of the chemical transformations of pentaphenylphosphorus, which was first obtained in 1953. The tetraorganylphosphonium salts were known much earlier, however, the features of the synthesis of transition metal complexes, which are usually obtained from tetraorganylphosphorus halides and metal halides, have not been sufficiently studied. The present review is devoted to the discussion of these topics, since the famous Wittig Reaction is associated with aryl phosphorus compounds, which allows synthesizing alkenes of a given structure, and derivatives of transition metals rightfully occupy a special place among catalysts of various chemical processes. The continuation of these classical studies in the field of chemistry of organoelemental compounds takes place at one of the leading universities in Russia - South Ural State University in the laboratory of chemistry of organoelemental compounds at the Faculty of Chemistry. This article aims at familiarizing the reader with the achievements of Professor V.V. Sharutin and his students in the field of organophosphorus compounds. The main attention is paid to the reactions of pentaphenylphosphorus and its derivatives, as well as methods for the synthesis of ionic complexes of silver, gold, copper, titanium, zirconium, hafnium, ruthenium, osmium, cobalt, rhodium, iridium, palladium and platinum with tetraorganylphosphonium cations. The structural features of the described compounds and the possibility of using transition metal complexes in some catalytic reactions are described.

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21

Tolmachev, A. A., E. V. Zarudnitskii, A. A. Yurchenko, and A. M. Pinchuk. "Phosphorylation of 2-phenyl-1,3,4-oxadiazole with phosphorus (III) halides." Chemistry of Heterocyclic Compounds 35, no. 9 (September 1999): 1117–19. http://dx.doi.org/10.1007/bf02251812.

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22

Lesikar, Leslie A., William D. Woodul, and Anne F. Richards. "The reactions of phosphorus(III) halides with β-diketiminato ligands." Polyhedron 26, no. 13 (August 2007): 3242–46. http://dx.doi.org/10.1016/j.poly.2007.03.004.

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23

Rabis, A., A. R. Grimmer, B. Thomas, E. Brendler, S. Beck, and M. Meisel. "Phosphorus-31 MAS NMR investigations of pyridine stabilized dithiomonometaphosphoryl halides." Solid State Nuclear Magnetic Resonance 28, no. 1 (July 2005): 57–63. http://dx.doi.org/10.1016/j.ssnmr.2005.06.001.

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24

Bezgubenko, L. V., S. E. Pipko, and A. D. Sinitsa. "Complexes of phosphorus halides with two or more coordination bonds." Russian Journal of General Chemistry 81, no. 8 (August 2011): 1596–614. http://dx.doi.org/10.1134/s1070363211080056.

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25

Kostyuk, Aleksandr N., Yurii V. Svyaschenko, Bogdan B. Barnych, Dmitriy A. Sibgatulin, Eduard B. Rusanov, and Dmitriy M. Volochnyuk. "Phosphorylation of derivatives of β-dialkyaminocrotonitriles with phosphorus(III) halides." Heteroatom Chemistry 20, no. 4 (2009): 194–201. http://dx.doi.org/10.1002/hc.20532.

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26

PINCHUK, A. M., A. A. TOLMACHEV, A. N. KOSTYUK, A. A. YURCHENKO, and A. I. SVIRIDON. "ChemInform Abstract: C-Phosphorylation of Azoles with Trivalent Phosphorus Halides." ChemInform 28, no. 11 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199711296.

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27

Tolmachew, Andrew A., Alexandra A. Chaikovskaya, Svetlana D. Kopteva, Aleksew O. Pushechnikov, and Sergei P. Ivonin. "C-Phosphorylation of Electron-Rich Heterocycles by Trivalent Phosphorus Halides." Phosphorus, Sulfur, and Silicon and the Related Elements 147, no. 1 (January 1, 1999): 483. http://dx.doi.org/10.1080/10426509908053721.

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28

Tattershall, Bruce W., Roger Blachnik, and Alexander Hepp. "Phosphorus NMR and ab initio study of pentaphosphorus dichalcogenide halides †." Journal of the Chemical Society, Dalton Transactions, no. 15 (2000): 2551–58. http://dx.doi.org/10.1039/b000613k.

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29

Kibardin, A. M., T. V. Gryaznova, P. I. Gryaznov, E. Ya Levi-Na, I. A. Litvinov, V. A. Naumov, Yu B. Mikhailov, A. N. Pudovik, and A. E. Arbuzov. "Reactions of Halides of Tervalent Phosphorus with Imines and -Diimines." Phosphorus, Sulfur, and Silicon and the Related Elements 51, no. 1-4 (September 1990): 183. http://dx.doi.org/10.1080/10426509008040717.

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30

Lee, Oh-Seuk, Kiyull Yang, Keum Duck Kang, In Sun Koo, Chan-Kyung Kim, and Ikchoon Lee. "Ab initio and DFT studies on hydrolyses of phosphorus halides." Journal of Computational Chemistry 25, no. 14 (2004): 1740–48. http://dx.doi.org/10.1002/jcc.20104.

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31

Schmidpeter, Alfred, Stefan Plank, and Kurt Polborn. "2-YIidvl-1,3,2-oxathiaphosphole und -oxaselenaphosphole / 2-Ylidyl-1,3,2-oxathiaphospholes and -oxaselenaphospholes." Zeitschrift für Naturforschung B 50, no. 10 (October 1, 1995): 1543–49. http://dx.doi.org/10.1515/znb-1995-1019.

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Ylidyl thioxophosphines or selenoxophosphines and phenacyl halides undergo addition in a 1:1 ratio and yield in the presence of triethylamine the title compounds. The molecular structure of an ylidyl oxathiaphosphole demonstrates a strong interaction between the ylid substituent and the heterocycle, making the exocyclic PC-bond unusually short and the endocyclic PO- and PS-bonds considerably longer than normal for a pyramidal phosphorus atom.The ylidyl chalcogenoxophosphines are oxidized by sulfur or selenium at the phosphorus atom and protonated at the ylidic carbon atom. No Wittig-type reaction is observed.

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32

Yorimitsu, Hideki. "Homolytic substitution at phosphorus for C–P bond formation in organic synthesis." Beilstein Journal of Organic Chemistry 9 (June 28, 2013): 1269–77. http://dx.doi.org/10.3762/bjoc.9.143.

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Organophosphorus compounds are important in organic chemistry. This review article covers emerging, powerful synthetic approaches to organophosphorus compounds by homolytic substitution at phosphorus with a carbon-centered radical. Phosphination reagents include diphosphines, chalcogenophosphines and stannylphosphines, which bear a weak P–heteroatom bond for homolysis. This article deals with two transformations, radical phosphination by addition across unsaturated C–C bonds and substitution of organic halides.

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33

Chua, Ming Hui, Kwok Wei Shah, Hui Zhou, and Jianwei Xu. "Recent Advances in Aggregation-Induced Emission Chemosensors for Anion Sensing." Molecules 24, no. 15 (July 25, 2019): 2711. http://dx.doi.org/10.3390/molecules24152711.

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The discovery of the aggregation-induced emission (AIE) phenomenon in the early 2000s not only has overcome persistent challenges caused by traditional aggregation-caused quenching (ACQ), but also has brought about new opportunities for the development of useful functional molecules. Through the years, AIE luminogens (AIEgens) have been widely studied for applications in the areas of biomedical and biological sensing, chemosensing, optoelectronics, and stimuli responsive materials. Particularly in the application of chemosensing, a myriad of novel AIE-based sensors has been developed to detect different neutral molecular, cationic and anionic species, with a rapid detection time, high sensitivity and high selectivity by monitoring fluorescence changes. This review thus summarises the recent development of AIE-based chemosensors for the detection of anionic species, including halides and halide-containing anions, cyanides, and sulphur-, phosphorus- and nitrogen- containing anions, as well as a few other anionic species, such as citrate, lactate and anionic surfactants.

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34

Budnikova, Yulia H., Tatyana V. Gryaznova, Valeriya V. Grinenko, Yulia B. Dudkina, and Mikhail N. Khrizanforov. "Eco-efficient electrocatalytic C–P bond formation." Pure and Applied Chemistry 89, no. 3 (March 1, 2017): 311–30. http://dx.doi.org/10.1515/pac-2016-1001.

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AbstractThe development of practical, efficient and atom-economical methods of formation of carbon-phosphorus bonds remains a topic of considerable interest for the current synthetic organic chemistry and electrochemistry. This review summarizes selected topics from the recent publications with particular emphasis on phosphine and phosphine oxides formation from white phosphorus, chlorophosphines in electrocatalytic processes using aryl, hetaryl or perfluoroalkyl halides as reagents. This review includes selected highlights concerning recent progress in modification of catalytic systems for aromatic C–H bonds phosphonation involving metal-catalyzed ligand directed or metal-induced oxidative processes. Furthermore, a part of this review is devoted to phosphorylation of olefins with white phosphorus under reductive conditions in water-organic media. Finally, we have also documented recent advances in ferrocene C–H activation and phosphorylation.

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35

Renard, Sylvie L., Julie Fisher, Colin A. Kilner, Mark Thornton-Pett, and Terence P. Kee. "On the mechanisms of degenerate halogen exchange in phosphorus(iii) halides." Journal of the Chemical Society, Dalton Transactions, no. 14 (June 24, 2002): 2921–32. http://dx.doi.org/10.1039/b202942c.

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36

Kibardin, A. M., T. V. Gryaznova, P. I. Gryaznov, E. Ya Levina, I. A. Litvinov, V. A. Naumov, Yu B. Mikhailov, and A. N. Pudovik. "Reactions of Halides of Tervalent Phosphorus with Imines and α-Diimines." Phosphorus, Sulfur, and Silicon and the Related Elements 51, no. 1 (1990): 183. http://dx.doi.org/10.1080/10426509008544235.

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37

Chaikovskaya, Aleksandra A., Yurii V. Dmitriv, Sergei P. Ivonin, Aleksandr M. Pinchuk, and Andrei A. Tolmachev. "Phosphorylation ofN-iso-propyl- andN-tert-butylpyrroles with phosphorus(III) halides." Heteroatom Chemistry 16, no. 7 (2005): 599–604. http://dx.doi.org/10.1002/hc.20158.

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38

NOVAK, I. "ChemInform Abstract: Molecular and Electronic Structure of Less Common Phosphorus Halides." ChemInform 23, no. 36 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199236001.

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39

Pipko, Sergey, Yuri Balitzky, and Anatoly Sinitsa. "Frozen Friedel-Krafts Type Reaction of Phosphorus Halides with Tetraphenylborate Anion." Phosphorus, Sulfur, and Silicon and the Related Elements 111, no. 1 (April 1, 1996): 103. http://dx.doi.org/10.1080/10426509608054732.

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40

Gusarova, N. K., B. A. Trofimov, S. F. Malysheva, T. N. Rakhmatulina, E. P. Vyalykh, and M. G. Voronkov. "Reaction of red phosphorus with benzyl halides in a superbase system." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 38, no. 2 (February 1989): 430. http://dx.doi.org/10.1007/bf00953650.

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41

Narain, R. P., and Devendra Kumar. "Adhesives produced by reactions of phosphorus halides with phenols and bisphenols." International Journal of Adhesion and Adhesives 12, no. 4 (October 1992): 271–74. http://dx.doi.org/10.1016/0143-7496(92)90065-4.

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42

Pavlov, V. A., N. V. Aristova, V. V. Moskva, G. F. Makhaeva, V. L. Yankovskaya, and V. V. Malygin. "Synthesis of phosphorus-containing formhydroxamoyl halides and their anticholine esterase properties." Pharmaceutical Chemistry Journal 25, no. 4 (April 1991): 255–58. http://dx.doi.org/10.1007/bf00772108.

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43

Böttcher, Tobias, Oleg Shyshkov, Matthias Bremer, Bassem S. Bassil, and Gerd-Volker Röschenthaler. "Carbene Complexes of Phosphorus(V) Fluorides by Oxidative Addition of 2,2-Difluorobis(dialkylamines) to Phosphorus(III) Halides." Organometallics 31, no. 4 (December 22, 2011): 1278–80. http://dx.doi.org/10.1021/om2009827.

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44

Kovalyova, Svetlana A., Sergey P. Ivonin, Andrey A. Tolmachev, and Alexander M. Pinchuk. "Phosphorylation of 2-( N , N -Dimethylaminomethylidenamino)thiophenes(furans) with Phosphorus(III) Halides." Phosphorus, Sulfur, and Silicon and the Related Elements 177, no. 8-9 (August 2002): 2183. http://dx.doi.org/10.1080/10426500213300.

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45

Wrackmeyer, Bernd, and Armando Ariza-Castolo. "Reactions Between Phosphorus Halides and (E)-1-Trimethylstannyl-2-Diethylboryl-1-Butene." Phosphorus, Sulfur, and Silicon and the Related Elements 90, no. 1-4 (May 1, 1994): 121–29. http://dx.doi.org/10.1080/10426509408016393.

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46

Paul, Martin, and Hubert Schmidbaur. "Coordination Chemistry of Dimethylgold Halides with Bidentate Phosphorus and Arsenic Ligands – Revisited." Chemische Berichte 129, no. 1 (January 1996): 77–83. http://dx.doi.org/10.1002/cber.19961290116.

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47

Chekotylo, Alexej A., Alexandr N. Kostyuk, Alexandr M. Pinchuk, and Andrej A. Tolmachev. "Reaction of ?-carbonyl substituted 1,3,3-trimethyl-2-methyleneindolines with phosphorus(III) halides." Heteroatom Chemistry 14, no. 1 (2003): 23–28. http://dx.doi.org/10.1002/hc.10060.

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48

KORMACHEV, V. V., O. A. KOLYAMSHIN, and YU N. MITRASOV. "ChemInform Abstract: Alkylation of Phosphorus-Containing CH-Acids with gem- Dichlorocyclopropylmethyl Halides." ChemInform 25, no. 29 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199429242.

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49

Bezgubenko, L. V., S. E. Pipko, and A. D. Sinitsa. "ChemInform Abstract: Complexes of Phosphorus Halides with Two or More Coordination Bonds." ChemInform 42, no. 50 (November 17, 2011): no. http://dx.doi.org/10.1002/chin.201150208.

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50

Tolmachev, A. A., E. V. Zarudnitskii, A. A. Yurchenko, and A. M. Pinchuk. "ChemInform Abstract: Phosphorylation of 2-Phenyl-1,3,4-oxadiazole with Phosphorus(III) Halides." ChemInform 31, no. 42 (October 17, 2000): no. http://dx.doi.org/10.1002/chin.200042114.

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