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Journal articles on the topic 'Dimethylbenzylamine'

Author: Grafiati

Published: 4 June 2021

Last updated: 8 February 2022

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1

Fleischer, Holger, and Dieter Schollmeyer. "Formation of meso-1,2-Bis(dimethylamino)-1,2-diphenylethane by Oxidative C-C Coupling Reaction." Zeitschrift für Naturforschung B 60, no. 10 (2005): 1083–87. http://dx.doi.org/10.1515/znb-2005-1011.

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The title compound was obtained from the reaction of N,N-dimethylbenzylamine with n-butyl lithium and sulfur in tetrahydrofuran at room temperature. Its molecular structure was investigated by means of single crystal X-ray diffraction and quantum chemical DFT methods. The formation of meso-1,2-bis(dimethylamino)-1,2-diphenylethane is likely to be due to an unusual α-deprotonation of N,N-dimethylbenzylamine, instead of the well known ortho-lithiation, with a subsequent oxidative C-C coupling of the anions. Ab initio calculations of the corresponding α- and o-deprotonated anions of N,N-dimethylb

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2

Mahmud, Tariq, Javed Iqbal, Muhammad Irshad, Mark R. J. Elsegood, and Vickie McKee. "Pentacarbonyl(N,N-dimethylbenzylamine)tungsten." Acta Crystallographica Section E Structure Reports Online 61, no. 9 (2005): m1789—m1791. http://dx.doi.org/10.1107/s1600536805025560.

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3

Cornaton, Yann, and Jean-Pierre Djukic. "A noncovalent interaction insight onto the concerted metallation deprotonation mechanism." Physical Chemistry Chemical Physics 21, no. 36 (2019): 20486–98. http://dx.doi.org/10.1039/c9cp03650d.

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4

Cormier, Morgan, Alexis Tabey, Thifanie Christine, Hélène Audrain, Eric Fouquet, and Philippe Hermange. "Synthesis and [*C]CO-labelling of (C,N) gem-dimethylbenzylamine–palladium complexes for potential applications in positron emission tomography." Dalton Transactions 50, no. 30 (2021): 10608–14. http://dx.doi.org/10.1039/d1dt01633d.

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<sup>13</sup>C- and <sup>11</sup>C-labelled conjugates were produced in one step upon carbonylation of homogeneous or heterogeneous arylpalladium complexes synthesised by mild C–H activation of gem-dimethylbenzylamine derivatives.

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5

Kafka, Stanislav, Petr Trška, Jan Kytner, Petr Taufmann, and Miloslav Ferles. "Hydroboration of N,N-dimethyl(2-vinylbenzyl)amine." Collection of Czechoslovak Chemical Communications 52, no. 8 (1987): 2047–56. http://dx.doi.org/10.1135/cccc19872047.

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Hydroboration of N,N-dimethyl(2-vinylbenzyl)amine followed by oxidation afforded a mixture of primary and secondary alcohol, i.e. 2-(2-dimethylaminomethylphenyl)ethanol and 1-(2-dimethylaminomethylphenyl)ethanol, together with the reduction product – 2-ethyl(N,N-dimethylbenzylamine).

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6

Li, S., E. R. Bernstien, and J. I. Seeman. "Stable conformations of benzylamine and N,N-dimethylbenzylamine." Journal of Physical Chemistry 96, no. 22 (1992): 8808–13. http://dx.doi.org/10.1021/j100201a023.

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7

Elmasmodi, Abdellatif, Didier Barbry, Bruno Hasiak, and Daniel Couturier. "Evolution thermique de derives des hexahydrobenzazocines-2 et des hexahydro-1H-benzazonines-2 N-quaternarises (ammoniums, N-oxydes)." Collection of Czechoslovak Chemical Communications 54, no. 10 (1989): 2767–74. http://dx.doi.org/10.1135/cccc19892767.

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La thermolyse des hydroxydes d’ammonium derives des hexahydrobenzazocines-2 et de la methyl-2-hexahydro-1H benzazonine-2 conduit a un melange de composes ethyleniques [butenyl-3 (ou pentenyl-4) N,N-dimethylbenzylamine et dimethylamino-1 orthotolyl-4 butene-3 (ou pentene-4)]. Les N-oxydes de N-methyl hexahydrobenzazocines-2 se decomposent thermiquement en derives de l’oxa-2 hexahydro-1H-benzazonines-3 souilles de la benzazocine de depart.

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8

Churches, Quentin I., Helen E. Stewart, Scott B. Cohen, Adam Shröder, Peter Turner, and Craig A. Hutton. "Stereoselectivity of the Petasis reaction with various chiral amines and styrenylboronic acids." Pure and Applied Chemistry 80, no. 4 (2008): 687–94. http://dx.doi.org/10.1351/pac200880040687.

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Several chiral amines were investigated for the stereoselective preparation of homophenylalanine derivatives using the Petasis reaction. Chiral secondary amines such as N,α-dimethylbenzylamine and N-benzylphenylglycinol gave the best results in terms of both yield and diastereoselectivity. The use of N-benzylphenylglycinol leads directly to 3-alkenyl-4-benzyl-5-phenyloxazin-2-one products. Intriguing variation was observed in the stereoselectivity of reactions employing para-substituted styrenylboronic acid substrates, where presumably only electronic factors are involved.

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9

Ma, Qing Lan, and Yuan Ming Huang. "Synthesis and Properties of UV-Curable Sealant for LCD Panels." Key Engineering Materials 428-429 (January 2010): 345–48. http://dx.doi.org/10.4028/www.scientific.net/kem.428-429.345.

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Ultraviolet curable sealant was synthesized by polymerizing epoxy resin with acrylic acid in the presence of catalyst N,N-dimethylbenzylamine. The synthesized ultraviolet-curable sealant could be solidified upon exposure to 365 nm ultraviolet irradiation for 8 seconds. The optical, mechanical and thermal properties of the ultraviolet-cured sealant were investigated with ultraviolet-visible spectrometer, tensile machine and differential scanning calorimetry, respectively. Our results demonstrated that the transparent and thermally stable sealant was strong enough for liquid crystal display pane

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10

LI, S., E. R. BERNSTEIN, and J. I. SEEMAN. "ChemInform Abstract: Stable Conformations of Benzylamine and N,N-Dimethylbenzylamine." ChemInform 24, no. 7 (2010): no. http://dx.doi.org/10.1002/chin.199307082.

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11

Inoue, Osamu, Rie Hosoi, Sotaro Momosaki та ін. "Ionic interaction of [11C]-N, α-dimethylbenzylamine (DMBA) in rodent brain". Annals of Nuclear Medicine 17, № 6 (2003): 469–73. http://dx.doi.org/10.1007/bf03006437.

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12

Ma, Qing Lan, and Yuan Ming Huang. "Dependence of Optical Properties of UV-Curable Sealant on Amount of Catalyst N, N-Dimethylbenzylamine." Key Engineering Materials 428-429 (January 2010): 398–401. http://dx.doi.org/10.4028/www.scientific.net/kem.428-429.398.

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In the presence of the catalyst N, N-dimethylbenzylamine, a series of ultraviolet-curable sealants 1-6 were synthesized by varying the catalyst amount from 0.5, 1.0, 1.5, 2.0, 2.5 and 3.0 part in the process of polymerizing the epoxy resin (25 parts) with acrylic acid (17.5 parts). After having been cured by UV light, the transmittance of equally-thick films of the sealants changed with the amount of the catalyst. Furthermore, we recorded the transmittance of UV-cured sealant films when aged in air at high temperatures. Our results have demonstrated that the amount of catalyst poses limited ef

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13

Nandi, Dilip K., Sunanda K. Palit, and Dibakar C. Deka. "Acid catalyzed pressure synthesis of N,N-dimethylbenzylamine from benzylamine and methanol." Journal of Chemical Technology & Biotechnology 38, no. 4 (2007): 243–51. http://dx.doi.org/10.1002/jctb.280380404.

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14

Alsters, Paul L., Herman T. Teunissen, Jaap Boersma, and Gerard van Koten. "The oxygenation of cyclopalladated N,N-dimethylbenzylamine derivatives with tert-butyl hydroperoxide." Recueil des Travaux Chimiques des Pays-Bas 109, no. 9 (2010): 487–89. http://dx.doi.org/10.1002/recl.19901090909.

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15

Kiyani, Hamzeh, and Mozhgan Sadat Jalali. "Facile and Efficient Access to Tetrahydrobenzo[b]pyrans Catalyzed by N,N-Dimethylbenzylamine." HETEROCYCLES 92, no. 1 (2016): 75. http://dx.doi.org/10.3987/com-15-13360.

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16

Behrle, Andrew C., та Joseph A. R. Schmidt. "Synthesis and Reactivity of Homoleptic α-MetalatedN,N-Dimethylbenzylamine Rare-Earth-Metal Complexes". Organometallics 30, № 15 (2011): 3915–18. http://dx.doi.org/10.1021/om200363z.

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17

Moro, Antonio Carlos, Gislaine Aparecida da Cunha, Ronan Farias Freire de Souza, et al. "C 2 ,N-dimethylbenzylamine cyclopalladated compounds: evaluation of cytotoxic, mutagenic and antitubercular activities." Medicinal Chemistry Research 24, no. 7 (2015): 2879–88. http://dx.doi.org/10.1007/s00044-015-1339-3.

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18

Irander, Krishna, Bengt Ståhlbom, Hans Welinder, and Bengt Åkesson. "Metachromatic Cells and Eosinophils in the Nasal Mucosa and N,N-Dimethylbenzylamine Exposure." Acta Oto-Laryngologica 117, no. 3 (1997): 433–36. http://dx.doi.org/10.3109/00016489709113417.

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19

Gambaryan, N. P., D. P. Del'tsova, Z. V. Safronova, and G. S. Kaitmazova. "Fluorine-containing imines. Communication 6. Reaction of hexafluoroacetone perfluoropivaloylimine with dimethylantline and dimethylbenzylamine." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 36, no. 9 (1987): 1873–75. http://dx.doi.org/10.1007/bf00958334.

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20

Stevanato, Alessandra, Antonio E. Mauro, and Adelino V. G. Netto. "Thermal and spectroscopic investigation on N,N-dimethylbenzylamine based cyclopalladated compounds containing isonicotinamide." Journal of Thermal Analysis and Calorimetry 97, no. 1 (2009): 149–52. http://dx.doi.org/10.1007/s10973-009-0251-9.

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21

Smith, Peter James, and Md Amin. "The effect of the nature of the amine leaving group on the nature of the E2 transition state for the reaction of 1-phenylethylammonium ions with sodium ethoxide in ethanol." Canadian Journal of Chemistry 67, no. 9 (1989): 1457–67. http://dx.doi.org/10.1139/v89-222.

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To investigate the effect of the leaving group on the elimination reaction of 1-phenylethylammonium ions with sodium ethoxide in ethanol at 60 °C, the reaction of seven different quaternary ammonium salts and their β-deuterated analogues with trimethylamine, N-methylpiperidine, N-methyldiethylamine, triethylamine, N,N-dimethylbenzylamine, tripropylamine, and N,N-diethylbenzylamine as leaving groups has been studied. In all cases the elimination, which was shown to proceed via the concerted E2 process, was accompanied by competing substitution reactions. Although a significant dependence of the

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22

Ge, Qianqian, Xiang Zhu, and Zhengjin Yang. "Highly Conductive and Water-Swelling Resistant Anion Exchange Membrane for Alkaline Fuel Cells." International Journal of Molecular Sciences 20, no. 14 (2019): 3470. http://dx.doi.org/10.3390/ijms20143470.

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To ameliorate the trade-off effect between ionic conductivity and water swelling of anion exchange membranes (AEMs), a crosslinked, hyperbranched membrane (C-HBM) combining the advantages of densely functionalization architecture and crosslinking structure was fabricated by the quaternization of the hyperbranched poly(4-vinylbenzyl chloride) (HB-PVBC) with a multiamine oligomer poly(N,N-Dimethylbenzylamine). The membrane displayed well-developed microphase separation morphology, as confirmed by small angle X-ray scattering (SAXS) and transmission electron microscopy (TEM). Moreover, the corres

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23

Ananthnag, Guddekoppa S., Namepalli Edukondalu, Joel T. Mague, and Maravanji S. Balakrishna. "Copper and palladium complexes of 2-(diphenylphosphino)-N,N-dimethylbenzylamine and its selenide derivative." Polyhedron 62 (October 2013): 203–7. http://dx.doi.org/10.1016/j.poly.2013.06.036.

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24

Prakash, A. M., S. Unnikrishnan, and K. V. Rao. "Synthesis and characterization of SAPO-5 molecular sieve using N,N-dimethylbenzylamine as template." Microporous Materials 2, no. 2 (1994): 83–89. http://dx.doi.org/10.1016/0927-6513(93)e0032-c.

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25

Kolay, Siddhartha, Ninad Ghavale, Amey Wadawale, Dasarathi Das, and Vimal K. Jain. "Binuclear Orthometalated N,N-Dimethylbenzylamine Complexes of Palladium(II): Synthesis, Structures and Thermal Behavior." Phosphorus, Sulfur, and Silicon and the Related Elements 188, no. 10 (2013): 1449–61. http://dx.doi.org/10.1080/10426507.2012.757608.

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26

ALSTERS, P. L., H. T. TEUNISSEN, J. BOERSMA, and G. VAN KOTEN. "ChemInform Abstract: The Oxygenation of Cyclopalladated N,N-Dimethylbenzylamine Derivatives with tert.-Butyl Hydroperoxide." ChemInform 22, no. 4 (2010): no. http://dx.doi.org/10.1002/chin.199104131.

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27

Fornies, Juan, Rafael Navarro, and Violeta Sicilia. "Neutral and cationic orthopalladated () complexes (  phenylazophenyl, dimethylbenzylamine, 8-methylquinoline, 2-methoxy-3-N,N-dimetrylaminopropyl)." Polyhedron 7, no. 24 (1988): 2659–65. http://dx.doi.org/10.1016/s0277-5387(00)83889-9.

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28

Ståhlbom, Bengt, Bengt Åkesson, and Bo Jönsson. "Experimental human exposure to N , N -dimethylbenzylamine: generation of a controlled atmosphere and biological monitoring." International Archives of Occupational and Environmental Health 70, no. 6 (1997): 393–98. http://dx.doi.org/10.1007/s004200050234.

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29

Mohamed, Mark F., Alexei A. Neverov, and R. Stan Brown. "An Immobilized Ortho-Palladated Dimethylbenzylamine Complex as an Efficient Catalyst for the Methanolysis of Phosphorothionate Pesticides." Inorganic Chemistry 48, no. 3 (2009): 1183–91. http://dx.doi.org/10.1021/ic801382e.

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30

PRAKASH, A. M., K. V. RAO, and S. UNNIKRISHNAN. "ChemInform Abstract: Synthesis and Characterization of CoAPO-5 Molecular Sieve Using N,N- Dimethylbenzylamine as Template." ChemInform 25, no. 3 (2010): no. http://dx.doi.org/10.1002/chin.199403027.

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31

Trumbo, D. L., B. E. Mote, A. S. Trevino, and M. van den Brink. "Copolymerization behavior of 3-isopropenyl-?,?-dimethylbenzylamine and a preliminary evaluation of the copolymers in thermoset coatings." Journal of Applied Polymer Science 82, no. 4 (2001): 1030–39. http://dx.doi.org/10.1002/app.1937.

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32

Lindahl, Mats, Kristina Irander, Christer Tagesson, and Bengt Ståhlbom. "Nasal lavage fluid and proteomics as means to identify the effects of the irritating epoxy chemical dimethylbenzylamine." Biomarkers 9, no. 1 (2004): 56–70. http://dx.doi.org/10.1080/13547500410001662005.

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33

Alonso, M. Aránzazu, Juan A. Casares, Pablo Espinet, Katerina Soulantica, A. Guy Orpen та Hirihattaya Phetmung. "Conformational Preferences Driven by theC-Methyl Substituent in Chelatedo-Diphenylphosphino-α-methyl-N,N-dimethylbenzylamine Rhodium Complexes". Inorganic Chemistry 42, № 12 (2003): 3856–64. http://dx.doi.org/10.1021/ic034117a.

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34

Kantchev, Eric Assen B., and Jackie Y. Ying. "Practical One-Pot, Three-Component Synthesis of N-Heterocyclic Carbene (NHC) Ligated Palladacycles Derived fromN,N-Dimethylbenzylamine." Organometallics 28, no. 1 (2009): 289–99. http://dx.doi.org/10.1021/om8008475.

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35

Behrle, Andrew C., та Joseph A. R. Schmidt. "Insertion Reactions and Catalytic Hydrophosphination of Heterocumulenes using α-Metalated N,N-Dimethylbenzylamine Rare-Earth-Metal Complexes". Organometallics 32, № 5 (2012): 1141–49. http://dx.doi.org/10.1021/om300807k.

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36

MAURO, Antonio E., Adelino V. G. NETTO, Antonio C. MORO, Janaina G. FERREIRA, Regina H. A. SANTOS та Eduardo T. de ALMEIDA. "Molecular and Crystal Structure of Di(μ-N,S-thiocyanato)-bis[(N,N-dimethylbenzylamine-C2,N)palladium(II)]". X-ray Structure Analysis Online 25 (2009): 65–66. http://dx.doi.org/10.2116/xraystruct.25.65.

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37

Petrov, Alex R., Oliver Thomas, Klaus Harms, Konstantin A. Rufanov та Jörg Sundermeyer. "Dramatic enhancement of the stability of rare-earth metal complexes with α-methyl substituted N,N-dimethylbenzylamine ligands". Journal of Organometallic Chemistry 695, № 25-26 (2010): 2738–46. http://dx.doi.org/10.1016/j.jorganchem.2010.09.042.

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38

Boutadla, Youcef, David L. Davies, Stuart A. Macgregor, and Amalia I. Poblador-Bahamonde. "Computational and synthetic studies on the cyclometallation reaction of dimethylbenzylamine with [IrCl2Cp*]2: role of the chelating base." Dalton Transactions, no. 30 (2009): 5887. http://dx.doi.org/10.1039/b905469c.

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39

Ma, Zhiyuan, Anli Xu, Yongqin Du, et al. "Density, viscosity, refractive index and conductivity of switchable hydrophilicity solvent systems: N,N -Dimethylbenzylamine, water and carbon dioxide." Fluid Phase Equilibria 459 (March 2018): 94–102. http://dx.doi.org/10.1016/j.fluid.2017.12.005.

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40

Green, Kerry-Ann, Paul T. Maragh, Kamaluddin Abdur-Rashid, Alan J. Lough, and Tara P. Dasgupta. "Benzimidazol-2-ylidene ligated palladacyclic complexes of N,N-dimethylbenzylamine – Synthesis and application to C–C coupling reactions." Inorganica Chimica Acta 449 (August 2016): 38–43. http://dx.doi.org/10.1016/j.ica.2016.04.048.

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41

Gorbunov, D. B., V. V. Ershov, and G. A. Nikiforov. "Salts of acyl halides and 3, 5-di-tert-butyl-4-hydroxy-N, N-dimethylbenzylamine in benzylation reactions." Russian Chemical Bulletin 42, no. 3 (1993): 481–85. http://dx.doi.org/10.1007/bf00698436.

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42

Ma, Jian-Fang, Yasushi Kojima, and Yasuhiro Yamamoto. "Reactions of palladium complex of N,N-dimethylbenzylamine with aromatic phosphines bearing the methoxy groups at the 2,6-positions." Journal of Organometallic Chemistry 616, no. 1-2 (2000): 149–56. http://dx.doi.org/10.1016/s0022-328x(00)00586-6.

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43

van Mier, G. P. M., J. A. Kanters, and S. Harder. "A tetrahedrally surrounded nickel(II) complex: the structure of dichloro[2-(diphenylphosphino)-N,N-dimethylbenzylamine-N,P]nickel(II)." Acta Crystallographica Section C Crystal Structure Communications 43, no. 12 (1987): 2327–30. http://dx.doi.org/10.1107/s0108270187087882.

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44

Panda, Arunashree, G. Mugesh, Harkesh B. Singh, and Ray J. Butcher. "Synthesis, Structure, and Reactivity of Organochalcogen (Se, Te) Compounds Derived from 1-(N,N-Dimethylamino)naphthalene andN,N-Dimethylbenzylamine." Organometallics 18, no. 10 (1999): 1986–93. http://dx.doi.org/10.1021/om9808312.

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45

Alsters, Paul L., Herman T. Teunissen, Jaap Boersma, Anthony L. Spek, and Gerard van Koten. "Oxygenation of cyclopalladated N,N-dimethylbenzylamine complexes by inorganic and organic peroxides: oxygen insertion into the palladium-carbon bond." Organometallics 12, no. 11 (1993): 4691–96. http://dx.doi.org/10.1021/om00035a068.

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46

Farooq, H. M., and M. Z. Iqbal. "Thermal decomposition pattern of N,N-dimethylbenzylamine complexes with silver (I), gold(III), zinc(II), cadmium(II) and mercury(II)." Journal of Analytical and Applied Pyrolysis 52, no. 2 (1999): 139–50. http://dx.doi.org/10.1016/s0165-2370(99)00049-2.

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47

GORBUNOV, D. B., V. V. ERSHOV, and G. A. NIKIFOROV. "ChemInform Abstract: Salts of Carbocyclic Acid Halides and 3,5-Di-tert-butyl-4-hydroxy-N,N- dimethylbenzylamine in Benzylation Reactions." ChemInform 25, no. 20 (2010): no. http://dx.doi.org/10.1002/chin.199420100.

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48

Kiyani, Hamzeh, and Mozhgan Sadat Jalali. "Facial and Efficient Access to Dihydropyrano[3,2-c]Chromenes via Three-Component Reaction Using N,N-Dimethylbenzylamine As a New Organocatalyst." Combinatorial Chemistry & High Throughput Screening 19, no. 4 (2016): 275–82. http://dx.doi.org/10.2174/1386207319666160310144315.

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49

Mahmud, Tariq, Javed Iqbal, Muhammad Imran, and Vickie Mckee. "Synthesis and Spectroscopic Studies of 2-Bromo N, N-Dimethylbenzylamine and Its Complexes with Mo(CO)6 and W(CO)6." Journal of Applied Sciences 7, no. 9 (2007): 1347–50. http://dx.doi.org/10.3923/jas.2007.1347.1350.

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50

Forniés, J., R. Navarro, V. Sicilia, and M. Tomás. "Mono or binuclear orthopalladated () complexes (=phenylazophenyl-C2,N1; dimethylbenzylamine-C2,N;8-methylquinoline-C8,N) containing terminal or bridging SPR3 ligands." Inorganica Chimica Acta 168, no. 2 (1990): 201–7. http://dx.doi.org/10.1016/s0020-1693(00)80943-3.

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