Relevant bibliographies by topics / -(2-aminoethyl)pyridine

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Academic literature on the topic '-(2-aminoethyl)pyridine'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "-(2-aminoethyl)pyridine"

1

Raghavaiah, P., R. Kuladeep, D. Narayana Rao, A. Jyothi Lakshmi, P. Srujana, and J. Subbalakshmi. "Bis-(1-(2-aminoethyl)piperidino), (2-(2-aminoethyl)pyridino) and (1-(2-aminoethyl)pyrrolidino)-substituted dicyanoquinodimethanes: consequences of flexible ethylene spacers with heterocyclic moieties and amine functionalities." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 72, no. 5 (2016): 709–15. http://dx.doi.org/10.1107/s2052520616009537.

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Heterocyclic building blocks possessing ethylene spacer and amine functionality such as 1-(2-aminoethyl)piperidine (1,2-AEPi), 2-(2-aminoethyl)pyridine (2,2-AEPy) and 1-(2-aminoethyl)pyrrolidine (1,2-AEPr) were reacted with tetracyanoquinodimethane (TCNQ) to give disubstituted compounds namely bis-(1-(2-aminoethyl)piperidino)dicyanoquinodimethane (1), bis-(2-(2-aminoethyl)pyridino)dicyanoquinodimethane (2) and bis-(1-(2-aminoethyl)pyrrolidino)dicyanoquinodimethane (3). Utilization of 1,2-AEPi, 2,2-AEPy and 1,2-AEPr as disubstituents on TCNQ has resulted in interesting crystal structures. Inter
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Khan, M. A. H., T. K. Prasad та M. V. Rajasekharan. "Silver(I) complexes of 2-(2-aminoethyl)pyridine: nitrate and perchlorate salts of bis[μ-2-(2-aminoethyl)pyridine-κ2N:N′]disilver(I)". Acta Crystallographica Section C Crystal Structure Communications 61, № 6 (2005): m281—m283. http://dx.doi.org/10.1107/s0108270105012448.

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3

Ghosh, Manami, Adinath Majee, Munirathinam Nethaji, and Tanmay Chattopadhyay. "Syntheses and characterization of trans-[NiL2(NCS)2][L=2-(aminomethyl) pyridine], trans-[(NSC)2][L′=2-(2-aminoethyl)pyridine] and trans-[(NSC)2] [L″=2-(2-methylaminoethyl)pyridine] complexes: X-ray single crystal structure of trans-[(NSC)2] [L′=2-(2-aminoethyl)pyridine]." Inorganica Chimica Acta 362, no. 6 (2009): 2052–55. http://dx.doi.org/10.1016/j.ica.2008.09.037.

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Heinisch, G., B. Matuszczak, S. Pachler, and D. Rakowitz. "The Inhibitory Activity of Diazinyl-Substituted Thiourea Derivatives on Human Immunodeficiency Virus Type 1 Reverse Transcriptase." Antiviral Chemistry and Chemotherapy 8, no. 5 (1997): 443–46. http://dx.doi.org/10.1177/095632029700800507.

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Starting from 2-(2-aminoethyl)pyridine, a series of N-diazinyl-N′-[2-(2-pyridyl)ethyl]thioureas was prepared via the (2-pyridyl)ethylisothiocyanate and was screened as non-nucleoside human immunodeficiency virus type 1 reverse transcriptase inhibitors. Derivatives bearing a 3-pyridazinyl or a 4-pyrimidinyl moiety turned out to be the most potent compounds. However, they exhibited less activity than nevirapine or trovirdine.
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Dukat, Małgorzata, Anna Ramunno, Rita Banzi, M. Imad Damaj, Billy Martin та Richard A. Glennon. "3-(2-Aminoethyl)pyridine analogs as α4β2 nicotinic cholinergic receptor ligands". Bioorganic & Medicinal Chemistry Letters 15, № 19 (2005): 4308–12. http://dx.doi.org/10.1016/j.bmcl.2005.06.053.

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6

Razak, I. A., H. K. Fun, K. Chinnakali, S. Shanmuga Sundara Raj, J. C. Liu та X. Z. You. "Di-μ-azido-bis{[2-(2-aminoethyl)pyridine-N,N']aquacopper(II)} diperchlorate". Acta Crystallographica Section C Crystal Structure Communications 55, № 11 (1999): 1764–66. http://dx.doi.org/10.1107/s0108270199008987.

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7

Khrizanforova, V. V., R. R. Fayzullin, E. B. Krasovskaya, and Yu H. Budnikova. "Reaction Between 2-(2-Aminoethyl)pyridine and Acenaphthenequinone in the Presence of ZnCl2." Russian Journal of General Chemistry 94, no. 3 (2024): 737–41. http://dx.doi.org/10.1134/s1070363224030253.

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8

Da Prada, M. "New Approaches to the Treatment of Age-Related Brain Disorders." Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 18, S3 (1991): 384–86. http://dx.doi.org/10.1017/s0317167100032492.

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ABSTRACT:Two novel reversible enzyme inhibitors involved in monoamine metabolism are described. The novel and reversible inhibitors are the catechol-O-methyl-transferase (COMT) inhibitor, Ro 40-7592 (3,4-dihydroxy-4'-methyl-5-nitrobenzophenone), and the monoamine oxidase type-B (MAO-B) inhibitor, Ro 19-6327 (N-(2-aminoethyl)-5-chloro-2-pyridine carboxamide HC1). These may be of special therapeutic benefit in Parkinson's and Alzheimer's diseases.
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Lodeiro, Carlos, Rufina Bastida, Emilia Bértolo, and Adolfo Rodríguez. "A new family of NxOy pyridine-containing macrocycles: Synthesis and characterization of their Y(III), Ln(III), Zn(II), and Cd(II) coordination compounds." Canadian Journal of Chemistry 82, no. 3 (2004): 437–47. http://dx.doi.org/10.1139/v03-214.

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Reaction between 2,6-bis(2-formylphenoxymethyl)pyridine and N,N-bis(3-aminopropyl)methylamine or tris(2-aminoethyl)amine has been used as the starting point for the synthesis of seven oxa-aza macrocyclic ligands, five of them never reported previously. They all feature different pendant arms, which provide a wide range of coordination possibilities. The Schiff base macrocycles L1 and L4 and their reduced ligands L2 and L5 are derived from 2,6-bis(2-formylphenoxymethyl)pyridine and tris(2-aminoethyl)amine or N,N-bis(3-aminopropyl)methylamine, respectively. The reaction of L1 with salicylaldehyd
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10

Hamamci, Sevim, Veysel T. Yilmaz та William T. A. Harrison. "Silver(I)-Saccharinato Complexes with 2-(Aminomethyl)pyridine and 2-(2-Aminoethyl)pyridine Ligands: [Ag(sac)(ampy)] and [Ag2(sac)2(μ-aepy)2]". Zeitschrift für Naturforschung B 60, № 9 (2005): 978–83. http://dx.doi.org/10.1515/znb-2005-0912.

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Two new saccharinato-silver(I) (sac) complexes, [Ag(sac)(ampy)] (1), and [Ag2(sac)2(μ-aepy)2] (2), [ampy = 2-(aminomethyl)pyridine, aepy = 2-(2-aminoethyl)pyridine], have been prepared and characterized by elemental analysis, IR spectroscopy, thermal analysis and single crystal X-ray diffraction. Complexes 1 and 2 crystallize in the monoclinic space group P21/c and triclinic space group P1̄, respectively. The silver(I) ions in both complexes 1 and 2 exhibit a distorted T-shaped AgN3 coordination geometry. 1 consists of individual molecules connected into chains by N-H···O hydrogen bonds. There
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Book chapters on the topic "-(2-aminoethyl)pyridine"

1

Pardasani, R. T., and P. Pardasani. "Magnetic properties of tetrameric nickel(II) complex with (2-aminoethyl)pyridine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_458.

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Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of cobalt(II) complex with {N,N′-2,2′-bis(aminoethyl)-methylamine-bis(3-carboxysalicylaldimine)} and pyridine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 2. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62466-1_388.

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You might also be interested in the extended bibliographies on the topic '-(2-aminoethyl)pyridine' for particular source types:
Journal articles
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