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Relevant bibliographies by topics / Dimethylbenzylamine

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Journal articles

Academic literature on the topic 'Dimethylbenzylamine'

Author: Grafiati

Published: 4 June 2021

Last updated: 8 February 2022

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Journal articles on the topic "Dimethylbenzylamine"

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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