Relevant bibliographies by topics / 2-aminobenzyl amine

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic '2-aminobenzyl amine'

Author: Grafiati
Published: 4 June 2021
Last updated: 13 February 2022

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Journal articles on the topic "2-aminobenzyl amine"

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Mitra, Abhijit, Pamela J. Seaton, and Kraig A. Wheeler. "N-(2-Aminobenzyl)-N,N-bis(quinolin-2-ylmethyl)amine." Acta Crystallographica Section C Crystal Structure Communications 62, no. 9 (2006): o581—o582. http://dx.doi.org/10.1107/s0108270106030502.

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Garza Rodríguez, Luis Ángel, Perla Elizondo Martínez, Sylvain Bernès, Blanca Nájera Martínez, and Nancy Pérez Rodríguez. "N,N′-Bis(2-aminobenzyl)ethane-1,2-diaminium dinitrate." Acta Crystallographica Section E Structure Reports Online 69, no. 11 (2013): o1643—o1644. http://dx.doi.org/10.1107/s1600536813027475.

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In the title salt, C16H24N42+·2NO3−, both the cation and anion are placed in general positions, although the cation displays non-crystallographic inversion symmetry, with the aliphatic chain extended in an all-transconformation. The benzene rings are almost parallel, with a dihedral angle between their mean planes of 3.3 (6)°. The nitrate ions are placed in the vicinity of the protonated amine groups, forming efficient N—H...O inter-ion hydrogen bonds. Each nitrate ion in the asymmetric unit bridges two symmetry-related cations, forming anR44(18) ring, a common motif in organic ammonium nitrat
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3

Chen, Jianbin, Helfried Neumann, Matthias Beller, and Xiao-Feng Wu. "Palladium-catalyzed synthesis of isoindoloquinazolinones via dicarbonylation of 1,2-dibromoarenes." Org. Biomol. Chem. 12, no. 31 (2014): 5835–38. http://dx.doi.org/10.1039/c4ob01103a.

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The first example of palladium-catalyzed carbonylative synthesis of isoindoloquinazolinones has been developed. Using 1,2-dibromobenzenes and 2-aminobenzyl amine as substrates, the products were isolated in moderate to good yields with the installation of two molecules of CO.
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4

Barham, Ahmad S. "Influence of pH on the Electropolymerisation of 2-Aminophenol and 2-Aminobenzyl Alcohol." Journal of New Materials for Electrochemical Systems 18, no. 1 (2015): 037–41. http://dx.doi.org/10.14447/jnmes.v18i1.387.

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The electrochemical oxidation and polymerisation of 2-aminophenol and 2-aminobenzyl alcohol in aqueous solutions of different pH values has been studied. Polymer films of the studied monomers on gold electrodes were synthesized. The behaviour of both monomers is quite different, illustrating the resonance effect of the hydroxyl group being bound directly to the benzene ring for 2-aminophenol. For each compound it is shown that oxidation in acidic solutions is most difficult due to the protonation of the amine group. These polymer films can be used for applications such as corrosion protection
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BHATTACHARYYA, S. "ChemInform Abstract: Facile Two-Step Synthesis of 2-((2′-Aminobenzyl)amino)benzyl Alcohol, a Naturally Occurring Amine from Justicia gendarussa." ChemInform 27, no. 6 (2010): no. http://dx.doi.org/10.1002/chin.199606277.

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6

Jamier, Vincent, Eskender Mume, Cyril Papamicaël, and Suzanne V. Smith. "The Influence of Amino Group Position on Aryl Moiety of SarAr on Metal Complexation and Protein Labelling." Australian Journal of Chemistry 69, no. 9 (2016): 1054. http://dx.doi.org/10.1071/ch15794.

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New hexaazamacrobicyclic cage bi-functional chelators (BFCs), 1-N-(3-aminobenzyl)-3,6,10,13,16,19-hexaazabicyclo[6.6.6]eicosane-1,8-diamine (m-SarAr) and 1-N-(2-aminobenzyl)-3,6,10,13,16,19-hexaazabicyclo[6.6.6]eicosane-1,8-diamine (o-SarAr), were synthesised. Their complexation with selected transitions metal ions i.e. CuII, CoII, and CdII was investigated over a range of pH at micromolar concentrations. CuII was complexed by m-SarAr and o-SarAr rapidly within 5 min in pH range of 5–9 at ambient temperature. In contrast, the complexation of CoII and CdII by these ligands was slower. The conju
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7

Efe, G. Ergun, та E. O. Schlemper. "Complexes of new amine-nitrogen substituted α-amine oxime ligands (p-aminobenzyl, p-nitrobenzyl and p-(aminomethyl)phenyl substituents): X-ray structures of p-aminobenzylamine oxime dihydrochloride, [Ni(aminobenzao)2]ClO4 and [Rh(nitrobenzao)2Cl2]". Polyhedron 12, № 23 (1993): 2869–75. http://dx.doi.org/10.1016/s0277-5387(00)80070-4.

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8

Sairaj, Vedavalli, Thothadri Srinivasan, Muthusamy Kandaswamy, and Devadasan Velmurugan. "(Z)-3-[(2-Aminobenzyl)amino]-1-phenylbut-2-en-1-one." Acta Crystallographica Section E Structure Reports Online 70, no. 7 (2014): o742. http://dx.doi.org/10.1107/s1600536814012070.

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In the title compound, C17H18N2O, the aromatic rings are almost normal to one another, making a dihedral angle of 89.00 (8)°. There is an intramolecular N—H...O hydrogen bond in the molecule enclosing anS(6) ring motif. In the crystal, molecules are linked by N—H...O hydrogen bonds, forming chains along [010].
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9

Horák, Václav, Yonco Mermersky, and Dalal B. Guirguis. "3,5-Di-tert-butyl-1,2-benzoquinone Cleaves a CC-bond in Vicinal Aminobenzyl Alcohols." Collection of Czechoslovak Chemical Communications 59, no. 1 (1994): 227–30. http://dx.doi.org/10.1135/cccc19940227.

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Two vicinal aminobenzyl alcohols, L-threo-1-(4-methylthiophenyl)-2-amino-1,3-propanediol (IIa) and 1-phenyl-2-amino-1,3-propanediol (IIb), underwent, under mild conditions, CC-bond cleavage with 3,5-di-tert-butyl-1,2-benzoquinone (I) producing in high yields 4-methylthiobenzaldehyde (Va) and benzaldehyde (Vb), respectively, and 2-hydroxymethyl-4,6-di-tert-butylbenzoxazole (VII). Ethanolamine (VIII) under identical conditions produced benzoxazole VII. The reported reaction is a second case in which quinone I mimics reactions of pyridoxal.
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10

Zhang, Shanshan, Zheng Wang, Qianrong Cao, et al. "Aza-crown compounds synthesised by the self-condensation of 2-amino-benzyl alcohol over a pincer ruthenium catalyst and applied in the transfer hydrogenation of ketones." Dalton Transactions 49, no. 44 (2020): 15821–27. http://dx.doi.org/10.1039/d0dt03257c.

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Dissertations / Theses on the topic "2-aminobenzyl amine"

1

Kaßner, Lysann. "Stickstoffhaltige Monomere zur Herstellung von Hybridmaterialien." Doctoral thesis, Universitätsbibliothek Chemnitz, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-171321.

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In der vorliegenden Arbeit wurden stickstoffhaltige Monomere ausgehend von aromatischen Aminen oder Lactamen durch Umsetzung mit Chlorsilanen synthetisiert. Die so erhaltenen Derivate wurden mit Hilfe spektroskopischer und thermischer Analysenmethoden umfassend charakterisiert. Auf Basis der stickstoffhaltigen Monomere wurden über unterschiedliche Synthesestrategien organisch-anorganische, nanostrukturierte Hybridmaterialien hergestellt. Durch die thermisch induzierte Zwillingspolymerisation der Monomere 2,2‘-Spirobi[3,4-dihydro-1H-1,3,2-benzodiazasilin] und 1,1’,4,4‘-Tetrahydro-2,2‘-spirobi[b
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Journal articles
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