Academic literature on the topic 'Boron Trifluoride Dietherate Complex'

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Journal articles on the topic "Boron Trifluoride Dietherate Complex"

1

Lang, Wuke, Weijiang Zhang, Yin Tang, Jiao Xu, and Lei Zhang. "Determination of boron trifluoride in boron trifluoride complex by fluoride ion selective electrode." Transactions of Tianjin University 22, no. 1 (2016): 83–88. http://dx.doi.org/10.1007/s12209-016-2646-6.

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2

Liu, Tian Yu, Wei Jiang Zhang, and Jiao Xu. "Study on Preparation of Boric Acid with Boron Trifluoride Methanol Complex." Applied Mechanics and Materials 733 (February 2015): 276–79. http://dx.doi.org/10.4028/www.scientific.net/amm.733.276.

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With boron trifluoride methanol complex as raw material, the hydrolysis reaction of boron trifluoride was used to prepare the boric acid. The addition of calcium carbonate is aim to remove the hydrogen fluoride generated in the reaction process, The ultimate objective is making the material being the product of boric acid maximum. Reaction time (T), the ratio of raw materials (molar ratio) and the amount of water were investigated in the influence of the purity and yield of boric acid. The conductivity of mixed solution was determined by conductivity meter, the results determines the end point
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3

Mokhtary, Masoud, and Faranak Najafizadeh. "Polyvinylpolypyrrolidone-Supported Boron Trifluoride; Highly Efficient Catalyst for the Synthesis ofN-tert-Butyl Amides." E-Journal of Chemistry 9, no. 2 (2012): 576–82. http://dx.doi.org/10.1155/2012/632574.

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Highly efficient method for the preparation ofN-tert-butyl amides by reaction of nitriles withtert-butyl acetate is described using polyvinylpolypyrrolidone-supported boron trifluoride (PVPP-BF3) at 70°C in good to excellent yields. Selective amidation of benzonitrile in the presence of acetonitrile was also achieved. polyvinylpolypyrrolidone-boron trifluoride complex shows non-corrosive and stable solid catalyst elevated Lewis acid property.
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4

Ryu, Seungmin, John A. Jackson, and Charles M. Thompson. "Methanolysis of phosphoramidates with boron trifluoride-methanol complex." Journal of Organic Chemistry 56, no. 16 (1991): 4999–5002. http://dx.doi.org/10.1021/jo00016a042.

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Cid, José A., Yong-Xia Wang, and Hatsuo Ishida. "Cationic Polymerization of Benzoxazine Monomers by Boron Trifluoride Complex." Polymers and Polymer Composites 7, no. 6 (1999): 409–20. http://dx.doi.org/10.1177/0967391119990706409.

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Purified monofunctional benzoxazine monomers have very low reactivity, and some of them do not polymerize at all after several hours using the usual thermally initiated method. In this work a boron trifluoride complex with water was used to initiate the polymerization of some of the monofunctional benzoxazine monomers that do not polymerize when heated. The reactions were studied by Fourier transform infrared spectroscopy. The influence of the amine basicity on reactivity was investigated as well as the behavior of a bifunctional monomer. A new proposition for the benzoxazine polymerization me
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Peebles, Sean A., Linghong Sun, Robert L. Kuczkowski, Lawrence M. Nxumalo, and Thomas A. Ford. "The structure of the boron trifluoride–sulfur dioxide complex." Journal of Molecular Structure 471, no. 1-3 (1998): 235–42. http://dx.doi.org/10.1016/s0022-2860(98)00447-5.

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7

Chen, C. S., and Eli M. Pearce. "The boron trifluoride monoethyl amine complex cured epoxy resins." Journal of Applied Polymer Science 37, no. 4 (1989): 1105–24. http://dx.doi.org/10.1002/app.1989.070370421.

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8

Anderson, Wayne K., and Gaifa Lai. "Boron Trifluoride-Diethyl Ether Complex Catalyzed Aromatic Amino-Claisen Rearrangements." Synthesis 1995, no. 10 (1995): 1287–90. http://dx.doi.org/10.1055/s-1995-4434.

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Ohsawa, Toshiyuki, and Katsumi Yoshino. "Electrochemical polymerization of benzene utilizing boron trifluoride ethyl ether complex." Synthetic Metals 17, no. 1-3 (1987): 601–6. http://dx.doi.org/10.1016/0379-6779(87)90805-8.

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10

Cambie, RC, KC Higgs, JJ Rustenhoven, and PS Rutledge. "Experiments Directed Towards the Synthesis of Anthracyclinones. XXIX. Fluoro-Substituted Tetracycles." Australian Journal of Chemistry 49, no. 7 (1996): 751. http://dx.doi.org/10.1071/ch9960751.

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Diastereoselective formation of 9-fluoro-9-methylanthracyclinones has been achieved by treating ortho-methallyl-substituted anthraquinonyl homochiral dioxans with boron trifluoride etherate . The demethoxy anthraquinonyl dioxan (16) underwent slow reaction to give exclusively the (7S,9R) fluoro tetracycle (21) in 58% yield. The dimethoxy anthraquinonyl dioxan (15) was less reactive, allowing other reactions to compete, but boron trifluoride -acetic acid complex effected rapid cyclization of (15) with high diastereoselectivity. Short reaction times with this reagent circumvented the formation o
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Book chapters on the topic "Boron Trifluoride Dietherate Complex"

1

Matteson, D. S. "Boron Trifluoride–Acetic Acid Complex." In Boron Compounds. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-006-00176.

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Matteson, D. S. "Synthesis of Boron Trifluoride–Diethyl Ether Complex." In Boron Compounds. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-006-00138.

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Matteson, D. S. "Boron Trifluoride–Diethyl Ether Complex and Its Derivatives." In Boron Compounds. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-006-00172.

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Subramanian, L. R. "Using Boron Trifluoride–Diethyl Ether Complex." In Three Carbon-Heteroatom Bonds: Nitriles, Isocyanides, and Derivatives. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-019-00048.

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Haufe, G. "Synthesis Using Boron Trifluoride–Diethyl Ether Complex." In Fluorine. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-034-00261.

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Leung, M. k., and T. Y. Luh. "Catalyzed by Boron Trifluoride–Diethyl Ether Complex." In Acetals: O/N, S/S, S/N, and N/N and Higher Heteroatom Analogues. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-030-00195.

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OLÁH, G., L. NOSZKÓ, and A. PAVLÁTH. "The Benzotrifluoride-Nitryl Fluoride-Boron Trifluoride Complex." In World Scientific Series in 20th Century Chemistry. World Scientific Publishing Company, 2003. http://dx.doi.org/10.1142/9789812791405_0009.

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Kibayashi, C., and N. Yamazaki. "Reductive Cleavage with Sodium Borohydride–Boron Trifluoride–Diethyl Ether Complex." In Acetals: O/N, S/S, S/N, and N/N and Higher Heteroatom Analogues. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-030-00047.

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9

"16. Introduction of Fluorine with Boron Trifluoride and Tetrafluoroboric Acid Complexes and Salts of Tetrafluoroboric Acid: 16.1. Introduction of Fluorine with Boron Trifluoride and Boron Trifluoride–Diethyl Ether Complex." In Organo-Fluorine Compounds, edited by Baasner, Hagemann, and Tatlow. Georg Thieme Verlag, 1998. http://dx.doi.org/10.1055/b-0035-111175.

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Sammakia, T., J. A. Abramite, and M. F. Sammons. "By the Action of Boron Trifluoride–Diethyl Ether Complex as a Catalyst." In Ene-X Compounds (X=S, Se, Te, N, P). Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-033-00525.

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