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Journal articles on the topic 'Zinc bromides'

Author: Grafiati

Published: 4 June 2021

Last updated: 13 February 2022

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1

Cedzynska, Krystyna. "Some properties of zinc-bromine cell electrolytes containing symmetrical ammonium bromides." Electrochimica Acta 34, no. 10 (October 1989): 1439–42. http://dx.doi.org/10.1016/0013-4686(89)87185-3.

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2

Cathro, K. J., K. Cedzynska, D. C. Constable, and P. M. Hoobin. "Selection of quaternary ammonium bromides for use in zinc/bromine cells." Journal of Power Sources 18, no. 4 (November 1986): 349–70. http://dx.doi.org/10.1016/0378-7753(86)80091-x.

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3

Guijarro, Albert, David M. Rosenberg, and Reuben D. Rieke. "The Reaction of Active Zinc with Organic Bromides." Journal of the American Chemical Society 121, no. 17 (May 1999): 4155–67. http://dx.doi.org/10.1021/ja9844478.

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4

Pei, Guojing, Wan Xu, and Juan Li. "Iron- and zinc-mediated reductive coupling of styrenes and alkyl bromides: mechanistic investigation using DFT calculations." Organic Chemistry Frontiers 8, no. 13 (2021): 3372–80. http://dx.doi.org/10.1039/d1qo00386k.

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5

Stick, R. V., K. A. Stubbs, D. M. G. Tilbrook, and A. G. Watts. "A New Catalyst for the Reductive Elimination of Acylated Glycosyl Bromides to Form Glycals." Australian Journal of Chemistry 55, no. 2 (2002): 83. http://dx.doi.org/10.1071/ch02011.

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Ethylene-N,N-bis(salicylideneiminato)oxovanadium(IV) {VO(salen)} has been developed as a useful catalyst for the reductive elimination of acylated glycosyl bromides to form glycals, both in the pyranose and furanose series, using zinc/ammonium chloride/methanol or zinc/acetic acid/acetonitrile.

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6

Stick, R. V., K. A. Stubbs, D. M. G. Tilbrook, and A. G. Watts. "Corrigendum to: A New Catalyst for the Reductive Elimination of Acylated Glycosyl Bromides to Form Glycals." Australian Journal of Chemistry 55, no. 4 (2002): iv. http://dx.doi.org/10.1071/ch02011_co.

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Ethylene-N,N-bis(salicylideneiminato)oxovanadium(IV) {VO(salen)} has been developed as a useful catalyst for the reductive elimination of acylated glycosyl bromides to form glycals, both in the pyranose and furanose series, using zinc/ammonium chloride/methanol or zinc/acetic acid/acetonitrile.

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7

Isley, Nicholas A., Matt S. Hageman, and Bruce H. Lipshutz. "Dehalogenation of functionalized alkyl halides in water at room temperature." Green Chemistry 17, no. 2 (2015): 893–97. http://dx.doi.org/10.1039/c4gc01733a.

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8

Klement, Ingo, Paul Knochel, Khi Chau, and Gérard Cahiez. "Preparation of alkylzinc bromides using a new Mn/Cu catalyzed bromine-zinc exchange reaction." Tetrahedron Letters 35, no. 8 (February 1994): 1177–80. http://dx.doi.org/10.1016/0040-4039(94)88017-4.

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9

Shu, Chutian, Kanwar Sidhu, Li Zhang, Xiao-jun Wang, Dhileepkumar Krishnamurthy, and Chris H. Senanayake. "Palladium-Catalyzed Cross-Coupling of Cyclopropylmagnesium Bromide with Aryl Bromides Mediated by Zinc Halide Additives." Journal of Organic Chemistry 75, no. 19 (October 2010): 6677–80. http://dx.doi.org/10.1021/jo100983c.

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10

Miao, Bukeyan, and Shengming Ma. "Zinc-mediated allylation of carbon dioxide—the LiOAc effect." Organic Chemistry Frontiers 2, no. 1 (2015): 65–68. http://dx.doi.org/10.1039/c4qo00300d.

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A direct carboxylation reaction of allylic bromides mediated by zinc powder with 1 atm of CO₂ provided by a balloon has been developed. The reaction occurred smoothly at room temperature in the presence of LiOAc with an excellent branched regioselectivity.

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11

Prună, Alina, V. Brânzoi, and F. Brânzoi. "Corrosion Inhibition of Zinc in KOH Solutions." Advanced Materials Research 23 (October 2007): 233–36. http://dx.doi.org/10.4028/www.scientific.net/amr.23.233.

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The influence of electrolyte additions on the corrosion of zinc in aqueous solutions of KOH has been determined using electrochemical and nonelectrochemical techniques. These included anodic and cathodic polarization resistance and potentiodynamic method. The inhibitors studied included ZnO and tetra-alkylammonium bromides in different concentrations. From the data provided corrosion currents were calculated. The effectiveness of the inhibitors was compared and it was found that combinations of zinc oxide with tetra-alkylammonium salts were the most effective. Surface analysis obtained with scanning electron microscopy (SEM) revealed morphology characteristics developed at the zinc surface.

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12

Yoder, C. H., R. W. Schaeffer, P. McWilliams, A. Rowand, X. Liu, and J. Shambeda. "The synthesis of copper/zinc solid solutions of hydroxyl carbonates, sulphates, nitrates, chlorides and bromides." Mineralogical Magazine 75, no. 5 (October 2011): 2573–82. http://dx.doi.org/10.1180/minmag.2011.075.5.2573.

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AbstractThe relative stabilities of the copper/zinc solid solutions of hydroxyl sulphates, carbonates, nitrates, chlorides and bromides were studied by attempting their preparation using a variety of methods. All of the naturally occurring solid solutions except rosasite were obtained as single phases. Rosasite crystallized in a mixture with malachite and calcium carbonate during a room temperature preparation from calcium carbonate, copper nitrate and zinc nitrate. The solid solution with the antlerite stoichiometry [endmember Cu3SO4(OH)4] as well as the nitrates were not produced by the methods employed. All of the natural polymorphs of Cu2(OH)3Cl were obtained and a new method for the preparation of botallackite is reported. Botallackite was found to be stable in solution for over a year, contrary to previous reports. A bromine-bearing analogue of botallackite was prepared. Compounds were characterized by X-ray diffractometry, which was used to determine the unit-cell parameters, and by atomic absorption spectroscopy. The relative instability of solid solutions with certain stoichiometries is discussed in terms of the Jahn-Teller effect and relative solubilities.

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13

Xu, Yun, Wenjun Wang, Yu Cai, Xia Yang, Peng George Wang, and Wei Zhao. "A convenient and efficient synthesis of glycals by zinc nanoparticles." RSC Adv. 4, no. 87 (2014): 46662–65. http://dx.doi.org/10.1039/c4ra08028a.

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A simple and efficient method for the synthesis of pyranoid glycals utilizing the reductive elimination of glycopyranosyl bromides by zinc nanoparticles in an acetate buffer is described. A variety of pyranoid glycal derivatives were obtained, especially for the synthesis of 6-deoxy-4,6-O-benzylidene and disaccharide glycals with good yields.

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14

Benischke, Andreas D., Irina Knoll, Alice Rérat, Corinne Gosmini, and Paul Knochel. "A practical cobalt-catalyzed cross-coupling of benzylic zinc reagents with aryl and heteroaryl bromides or chlorides." Chemical Communications 52, no. 15 (2016): 3171–74. http://dx.doi.org/10.1039/c5cc10272c.

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A catalytic system consisting of 5 mol% CoCl₂ and 10 mol% isoquinoline allows a convenient cross-coupling of benzylic zinc reagents with various aryl and heteroaryl bromides or chlorides leading to polyfunctionalized diaryl- and aryl-heteroaryl-methane derivatives.

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15

Shu, Chutian, Kanwar Sidhu, Li Zhang, Xiao-jun Wang, Dhileepkumar Krishnamurthy, and Chris H. Senanayake. "ChemInform Abstract: Palladium-Catalyzed Cross-Coupling of Cyclopropylmagnesium Bromide with Aryl Bromides Mediated by Zinc Halide Additives." ChemInform 42, no. 5 (January 7, 2011): no. http://dx.doi.org/10.1002/chin.201105082.

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16

KLEMENT, I., P. KNOCHEL, K. CHAU, and G. CAHIEZ. "ChemInform Abstract: Preparation of Alkylzinc Bromides Using a New Mn/Cu Catalyzed Bromine- Zinc Exchange Reaction." ChemInform 25, no. 28 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199428128.

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17

Stadtmüller, Heinz, Björn Greve, Klaus Lennick, Abdellatif Chair, and Paul Knochel. "Preparation of Secondary Alkyl and Benzylic Zinc Bromides Using Activated Zinc Metal Deposited on Titanium Oxide." Synthesis 1995, no. 01 (January 1995): 69–72. http://dx.doi.org/10.1055/s-1995-3855.

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18

Klabunde, Kenneth J., and Renzo Campostrini. "Perfluoro-N-octylpalladium and -zinc bromides. remarkably stable coordinatively unsaturated organometallics." Journal of Fluorine Chemistry 42, no. 1 (January 1989): 93–104. http://dx.doi.org/10.1016/s0022-1139(00)83971-8.

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19

Knochel, P., A. Krasovskiy, V. Malakhov, and A. Gavryushin. "Direct LiCl-Promoted Insertion of Zinc into Organic Iodides and Bromides." Synfacts 2007, no. 1 (January 2007): 0079. http://dx.doi.org/10.1055/s-2006-955709.

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20

Hansen, Steven W., Terence D. Spawn, and Donald J. Burton. "The stereospecific preparation of fluorinated vinyl zinc reagents from polyfluorinated vinyl iodides or bromides and zinc metal." Journal of Fluorine Chemistry 35, no. 2 (March 1987): 415–20. http://dx.doi.org/10.1016/s0022-1139(00)85023-x.

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21

Zheng, Songlin, and Songlin Zhang. "Synthesis of allyl-aziridines from α-halo oxime ethers and allyl zinc bromides." RSC Advances 6, no. 31 (2016): 26437–40. http://dx.doi.org/10.1039/c5ra26394h.

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A novel method for the preparation of allyl aziridines by reacting α-halo oxime ethers with allylic zinc reagents under mild conditions. Some advantages of using organozinc reagents are that they are easily prepared, non-toxic, and more selective than Grignard reagents.

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22

Knochel, P., and J. F. Normant. "Diastereoselective addition of functionalized allylic zinc bromides to alkenyl organometallics. Part 5." Tetrahedron Letters 27, no. 47 (1986): 5727–30. http://dx.doi.org/10.1016/s0040-4039(00)85311-3.

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23

MAEDA, Hatsuo, Junko KAWABATA, and Hidenobu OHMORI. "Allylation of Aldehydes with Allyl Bromides and Zinc Induced by Pyridinium Perchlorates." CHEMICAL & PHARMACEUTICAL BULLETIN 40, no. 10 (1992): 2834–35. http://dx.doi.org/10.1248/cpb.40.2834.

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24

STADTMUELLER, H., B. GREVE, K. LENNICK, A. CHAIR, and P. KNOCHEL. "ChemInform Abstract: Preparation of Secondary Alkyl and Benzylic Zinc Bromides Using Activated Zinc Metal Deposited on Titanium Oxide." ChemInform 26, no. 34 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199534100.

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25

Breton, Gary, John Shugart, Christine Hughey, Brian Conrad, and Suzanne Perala. "Use of Cyclic Allylic Bromides in the Zinc–Mediated Aqueous Barbier–Grignard Reaction." Molecules 6, no. 8 (July 31, 2001): 655–62. http://dx.doi.org/10.3390/60800655.

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26

Guijarro, Albert, and Reuben D. Rieke. "Structure-Reactivity Relationship in the Reaction of Highly Reactive Zinc with Alkyl Bromides." Angewandte Chemie International Edition 37, no. 12 (July 3, 1998): 1679–81. http://dx.doi.org/10.1002/(sici)1521-3773(19980703)37:12<1679::aid-anie1679>3.0.co;2-b.

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27

MAEDA, H., J. KAWABATA, and H. OHMORI. "ChemInform Abstract: Allylation of Aldehydes with Allyl Bromides and Zinc Induced by Pyridinium Perchlorates." ChemInform 24, no. 42 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199342112.

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28

Mukherjee, Chinmoy, Pallavi Tiwari, and Anup Kumar Misra. "Synthesis of thio- and selenoglycosides by cleavage of dichalconides in the presence of zinc/zinc chloride and reaction with glycosyl bromides." Tetrahedron Letters 47, no. 4 (January 2006): 441–45. http://dx.doi.org/10.1016/j.tetlet.2005.11.074.

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29

Polat, Tülay, and Robert J. Linhardt. "Zinc triflate–benzoyl bromide: a versatile reagent for the conversion of ether into benzoate protecting groups and ether glycosides into glycosyl bromides." Carbohydrate Research 338, no. 5 (February 2003): 447–49. http://dx.doi.org/10.1016/s0008-6215(02)00481-0.

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30

Knecht, Manfred, and Wilhelm Boland. "(E)-Selective Alkylidenation of Aldehydes with Reagents derived from α-Acetoxy bromides, Zinc and CrCI3." Synlett 1993, no. 11 (1993): 837–38. http://dx.doi.org/10.1055/s-1993-22625.

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31

Schade, Matthias A., Albrecht Metzger, Stephan Hug, and Paul Knochel. "Nickel-catalyzed cross-coupling reactions of benzylic zinc reagents with aromatic bromides, chlorides and tosylates." Chemical Communications, no. 26 (2008): 3046. http://dx.doi.org/10.1039/b803072c.

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32

GUIJARRO, A., and R. D. RIEKE. "ChemInform Abstract: Structure-Reactivity Relationship in the Reaction of Highly Reactive Zinc with Alkyl Bromides." ChemInform 29, no. 45 (June 19, 2010): no. http://dx.doi.org/10.1002/chin.199845069.

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33

Lebedev, S. A., V. S. Lopatina, R. S. Sorokina, S. S. Berestova, E. S. Petrov, and I. P. Beletskaya. "Condensation of aryl bromides with styrenes, catalyzed by nickel complexes in the presence of zinc." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 36, no. 11 (November 1987): 2329–32. http://dx.doi.org/10.1007/bf00957309.

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34

Tang, Shi, Dong Zhou, Shu-hua Li, and Nai-xing Wang. "Stereoselective palladium-catalyzed cross-coupling of (2-amido-1-phenylpropyl)zinc compounds with aryl bromides." Chemical Research in Chinese Universities 29, no. 4 (July 11, 2013): 678–81. http://dx.doi.org/10.1007/s40242-013-3057-z.

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35

Majee, Adinath, Asish R. Das, and Brindaban C. Ranu. "ChemInform Abstract: Zinc Mediated Allylation of Aldehydes and Ketones Using Allyl Bromides and Commercial Zinc Dust. The Issue of Regio- and Stereoselectivity." ChemInform 30, no. 9 (June 17, 2010): no. http://dx.doi.org/10.1002/chin.199909043.

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36

Keerthi Krishnan, K., Salim Saranya, K. R. Rohit, and Gopinathan Anilkumar. "A novel zinc-catalyzed Suzuki-type cross-coupling reaction of aryl boronic acids with alkynyl bromides." Journal of Catalysis 372 (April 2019): 266–71. http://dx.doi.org/10.1016/j.jcat.2019.03.005.

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37

He, Yan, Shenghai Guo, Xinying Zhang, and Xuesen Fan. "Zinc-Mediated One-Pot Tandem Reaction of Nitriles with Propargyl Bromides: An Access to 3-Alkynylpyridines." Journal of Organic Chemistry 79, no. 21 (October 10, 2014): 10611–18. http://dx.doi.org/10.1021/jo501869d.

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38

Shin, Ueon Sang, Kyung-Hwan Cho, and Seung-Hoi Kim. "Preparation 2-Substituted-4-pyridylzinc Bromides via Direct Insertion of Active Zinc and Their Coupling Reactions." Bulletin of the Korean Chemical Society 34, no. 5 (May 20, 2013): 1575–78. http://dx.doi.org/10.5012/bkcs.2013.34.5.1575.

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39

Lebedev, S. A., V. S. Lopatina, E. S. Petrov, and I. P. Beletskaya. "Condensation of organic bromides with vinyl compounds catalysed by nickel complexes in the presence of zinc." Journal of Organometallic Chemistry 344, no. 2 (April 1988): 253–59. http://dx.doi.org/10.1016/0022-328x(88)80484-4.

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40

Yanai, Kei, and Hideo Togo. "Novel preparation of N-arylmethyl-N-arylmethyleneamine N-oxides from benzylic bromides with zinc and isobutyl nitrite." Tetrahedron 75, no. 25 (June 2019): 3523–29. http://dx.doi.org/10.1016/j.tet.2019.05.012.

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41

Kurono, Nobuhito, Tomio Inoue, and Masao Tokuda. "Facile preparation of organozinc bromides using electrogenerated highly reactive zinc and its use in cross-coupling reaction." Tetrahedron 61, no. 47 (November 2005): 11125–31. http://dx.doi.org/10.1016/j.tet.2005.09.031.

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42

Liu, Yongan, Qiongzhen Lin, Zhiwei Xiao, Changge Zheng, Yong Guo, Qing-Yun Chen, and Chao Liu. "Zinc-Mediated Intermolecular Reductive Radical Fluoroalkylsulfination of Unsaturated Carbon-Carbon Bonds with Fluoroalkyl Bromides and Sulfur Dioxide." Chemistry - A European Journal 25, no. 7 (January 7, 2019): 1824–28. http://dx.doi.org/10.1002/chem.201805526.

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43

Krasovskiy, Arkady, Vladimir Malakhov, Andrei Gavryushin, and Paul Knochel. "Efficient Synthesis of Functionalized Organozinc Compounds by the Direct Insertion of Zinc into Organic Iodides and Bromides." Angewandte Chemie International Edition 45, no. 36 (September 11, 2006): 6040–44. http://dx.doi.org/10.1002/anie.200601450.

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44

KNECHT, M., and W. BOLAND. "ChemInform Abstract: E-Selective Alkylidenation of Aldehydes with Reagents Derived from . alpha.-Acetoxy Bromides, Zinc, and CrCl3." ChemInform 25, no. 35 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199435097.

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45

Yoder, C. H., R. W. Schaeffer, P. McWilliams, A. Rowand, X. Liu, and J. Shambeda. "ChemInform Abstract: The Synthesis of Copper/Zinc Solid Solutions of Hydroxyl Carbonates, Sulfates, Nitrates, Chlorides and Bromides." ChemInform 43, no. 29 (June 21, 2012): no. http://dx.doi.org/10.1002/chin.201229227.

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46

Andersen, Thomas L., Aske S. Donslund, Karoline T. Neumann, and Troels Skrydstrup. "Carbonylative Coupling of Alkyl Zinc Reagents with Benzyl Bromides Catalyzed by a Nickel/NN 2 Pincer Ligand Complex." Angewandte Chemie International Edition 57, no. 3 (January 15, 2018): 800–804. http://dx.doi.org/10.1002/anie.201710089.

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47

Paul, Jérôme, Tania Xavier, Marc Presset, Erwan Le Gall, Eric Léonel, Christophe Pichon, and Sylvie Condon. "Cobalt-Zinc-Diimine Multicatalysis: Enhanced syn Diastereoselectivity in the Reductive Multicomponent Coupling of Aryl Bromides, Acrylates and Aldehydes." ChemistrySelect 3, no. 47 (December 18, 2018): 13480–86. http://dx.doi.org/10.1002/slct.201803710.

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48

He, Yan, Shenghai Guo, Xinying Zhang, and Xuesen Fan. "ChemInform Abstract: Zinc-Mediated One-Pot Tandem Reaction of Nitriles with Propargyl Bromides: An Access to 3-Alkynylpyridines." ChemInform 46, no. 16 (April 2015): no. http://dx.doi.org/10.1002/chin.201516218.

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49

Andersen, Thomas L., Aske S. Donslund, Karoline T. Neumann, and Troels Skrydstrup. "Carbonylative Coupling of Alkyl Zinc Reagents with Benzyl Bromides Catalyzed by a Nickel/NN 2 Pincer Ligand Complex." Angewandte Chemie 130, no. 3 (December 18, 2017): 808–12. http://dx.doi.org/10.1002/ange.201710089.

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50

Marton, Daniele, Umberto Russo, Diego Stivanello, Giuseppe Tagliavini, Paolo Ganis, and Giovanni Carlo Valle. "Preparation of Benzylstannanes by Zinc-Mediated Coupling of Benzyl Bromides with Organotin Derivatives. Physicochemical Characterization and Crystal Structures." Organometallics 15, no. 6 (January 1996): 1645–50. http://dx.doi.org/10.1021/om9507742.

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