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Journal articles on the topic '2-aminobenzyl amine'

Author: Grafiati

Published: 4 June 2021

Last updated: 13 February 2022

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1

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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2

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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5

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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11

Dey, D. K., S. P. Dey, A. Elmali, and Y. Elerman. "Crystal Structure and Conformation of 2-{(2′-Aminobenzyl)iminoethyl}- 5-methoxyphenol." Zeitschrift für Naturforschung B 56, no. 4-5 (2001): 375–80. http://dx.doi.org/10.1515/znb-2001-4-509.

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AbstractThe Schiff base, 2-{(2′-aminobenzyl)iminoethyl}-5-methoxyphenol, 1,2 -C6H4[NH2-2 ʹ]-CH2N=CHC6H3(OMe-5)OH (I), has been prepared by the reaction of 2 -amino-1-benzylamine and 2-hydroxy-4-methoxyacetophenone in methanol. The molecular structure has been confirmed by single crystal X-ray crystallography (triclinic, space group P 1̄, a = 7.201(2), b = 9.802(2), c = 9.993(2) Å, α = 83.09(2), β = 73.49(2), γ = 84.09(2)°, R = 0.0415 for 2611 independent reflections). The 1H and 13C NMR spectra in CDCI3 solution indicate the formation of some other minor conformations or dissociation in solu

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12

Chism, John P., and Douglas E. Rickert. "In vitro activation of 2-aminobenzyl alcohol and 2-amino-6-nitrobenzyl alcohol, metabolites of 2-nitrotoluene and 2,6-dinitrotoluene." Chemical Research in Toxicology 2, no. 3 (1989): 150–56. http://dx.doi.org/10.1021/tx00009a005.

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13

Jong, Jacobus A. W., Xu Bao, Qian Wang, and Jieping Zhu. "Formal [4+1] Cycloaddition ofo‐Aminobenzyl Chlorides with Isocyanides: Synthesis of 2‐Amino‐3‐Substituted Indoles." Helvetica Chimica Acta 102, no. 3 (2019): e1900002. http://dx.doi.org/10.1002/hlca.201900002.

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14

Hirai, K., H. Koike, T. Ishiba, et al. "Amino acid amides of 2-[(2-aminobenzyl)sulfinyl]benzimidazole as acid-stable prodrugs of potential inhibitors of H+K+ ATPase." European Journal of Medicinal Chemistry 26, no. 2 (1991): 143–58. http://dx.doi.org/10.1016/0223-5234(91)90024-h.

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15

Capozzi, Maria Annunziata M., Giancarlo Terraneo та Cosimo Cardellicchio. "Structural insights into methyl- or methoxy-substituted 1-(α-aminobenzyl)-2-naphthol structures: the role of C—H...π interactions". Acta Crystallographica Section C Structural Chemistry 75, № 2 (2019): 189–95. http://dx.doi.org/10.1107/s2053229619001050.

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Aminobenzylnaphthols are a class of compounds containing a large aromatic molecular surface which makes them suitable candidates to study the role of C—H...π interactions. We have investigated the effect of methyl or methoxy substituents on the assembling of aromatic units by preparing and determining the crystal structures of (S,S)-1-{(4-methylphenyl)[(1-phenylethyl)amino]methyl}naphthalen-2-ol, C26H25NO, and (S,S)-1-{(4-methoxyphenyl)[(1-phenylethyl)amino]methyl}naphthalen-2-ol, C26H25NO2. The methyl group influenced the overall crystal packing even if the H atoms of the methyl group did not

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16

Lehr, Philipp, Andreas Billich, Brigitte Charpiot, et al. "Inhibitors of Human Immunodeficiency Virus Type 1 Protease Containing 2-Aminobenzyl-Substituted 4-Amino-3-hydroxy-5-phenylpentanoic Acid: Synthesis, Activity, and Oral Bioavailability." Journal of Medicinal Chemistry 39, no. 10 (1996): 2060–67. http://dx.doi.org/10.1021/jm9508696.

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17

Latha, V., B. Annaraj, and M. A. Neelakantan. "ESIPT inspired dual fluorescent probe (Z)-3-((4-(4-aminobenzyl) phenyl) amino)-1,3-diphenylprop-2-en-1-one: Experimental and DFT based approach to photophysical properties." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 133 (December 2014): 44–53. http://dx.doi.org/10.1016/j.saa.2014.04.192.

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18

Saemian, Nader, Gholamhossein Shirvani, Sayed Sajad Oliyaee та Mohsen Javaheri. "A convenient method for 14C-labeling of 2-methylthio-1-[4-N-α-ethoxycarbonylbenzyl)-amino-benzyl]-5-hydroxymethyl-2-[14C]-1H-imidazole and 1-[4-N-α-ethoxy-carbonylbenzyl)-aminobenzyl]-5-hydroxymethyl-2-[14C]-1H-imidazole as potential antihypertensives". Journal of Radioanalytical and Nuclear Chemistry 292, № 1 (2011): 237–41. http://dx.doi.org/10.1007/s10967-011-1484-1.

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