Relevant bibliographies by topics / 2-Aminopyridine

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic '2-Aminopyridine'

Author: Grafiati
Published: 2 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "2-Aminopyridine"

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Tran, C., M. Haddad, and V. Ratovelomanana-Vidal. "Ruthenium-Catalyzed, Microwave-Mediated [2+2+2] Cycloaddition: A Useful Combination for the Synthesis of 2-Aminopyridines." Synlett 30, no. 16 (2019): 1891–94. http://dx.doi.org/10.1055/s-0037-1611920.

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A ruthenium-catalyzed [2+2+2] cycloaddition between α,ω-diynes and cyanamides is reported under microwave irradiation to access 2-aminopyridines. In contrast to the classical thermal conditions, this atom-economical sustainable protocol allows access to diverse functionalized 2-aminopyridine derivatives with high yields and excellent regioselectivities in MeTHF with short reaction times.
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Li, Zongyang, Yaxuan Li, Wenxu Chang, et al. "Synthesis and Fluorescent Properties of Aminopyridines and the Application in “Click and Probing”." Molecules 27, no. 5 (2022): 1596. http://dx.doi.org/10.3390/molecules27051596.

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Unsubstituted pyridin-2-amine has a high quantum yield and is a potential scaffold for a fluorescent probe. However, the facile access to conjugated highly substituted aminopyridines and the study of their fluorescent properties is scarce. In this paper, synthesis and fluorescent properties of multisubstituted aminopyridines were studied based on a recently developed Rh-catalyzed coupling of vinyl azide with isonitrile to form a vinyl carbodiimide intermediate, following tandem cyclization with an alkyne. An aminopyridine substituted with an azide group as a potential probe was further designe
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Netto, A. Marques, S. M. C. M. Bicalho, Ca L. Filgueiras, and J. C. Machado. "Positron annihilation studies in solid 2-aminopyridine, 3-aminopyridine, 4-aminopyridine and 2-aminopyrimidine." Chemical Physics Letters 119, no. 6 (1985): 507–10. http://dx.doi.org/10.1016/0009-2614(85)85378-1.

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Benzenine, Djamila, Zahira Kibou, Fatima Belhadj, et al. "Efficient Multicomponent Catalyst-Free Synthesis of Substituted 2-Aminopyridines." Chemistry Proceedings 3, no. 1 (2020): 125. http://dx.doi.org/10.3390/ecsoc-24-08381.

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2-aminopyridines scaffolds are an important class of nitrogen heterocyclic compounds with a wide range of biological activities. Multicomponent reactions (MCRs) are useful methods for the construction of nitrogen heterocyclic compounds. In this context, syntheses of 2-aminopyridines derivatives via MCRs have attracted considerable attention in recent years. We present, in this work, a rapid and efficient synthesis of 2-aminopyridine derivatives, via the catalyst-free four-component method. This protocol provides a simple and practical approach to functionalized 2-aminopyridnes from readily ava
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Comins, Daniel L. "Synthesis of MAPA Reagents and 2-Alkyl(aryl)aminopyridines from 2-Bromopyridine Using the Goldberg Reaction." Molecules 27, no. 6 (2022): 1833. http://dx.doi.org/10.3390/molecules27061833.

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A short and economical synthesis of various 2-methylaminopyidine amides (MAPA) from 2-bromopyridine has been developed using the catalytic Goldberg reaction. The effective catalyst was formed in situ by the reaction of CuI and 1,10-phenanthroline in a 1/1 ratio with a final loading of 0.5–3 mol%. The process affords high yields and can accommodate multigram-scale reactions. A modification of this method provides a new preparation of 2-N-substituted aminopyridines from various secondary N-alkyl(aryl)formamides and 2-bromopyridine. The intermediate aminopyridine formamide is cleaved in situ thro
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Ogurtsova, D. N., I. V. Palamarchuk, and I. Kulakov. "Synthesis of monothiooxamide derivatives based on chloroacetamides of 3-aminopyridin-2(1n)-ones." BULLETIN of the L.N. Gumilyov Eurasian National University. Chemistry. Geography. Ecology Series 139, no. 2 (2022): 28–32. http://dx.doi.org/10.32523/2616-6771-2022-139-2-28-32.

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On the basis of biologically active 3-aminopyridine-2(1H)-ones, the authors carried out chemical modification into derivatives of the corresponding monothiooxamides for the first time. It has been shown that monothiooxamides of 3-aminopyridin-2(1H)-oneenter into transamidation reactions with hydrazine-hydrate and are further cyclized under the action of chloroacetyl chloride into conjugated 1,3,4-thiadizole derivatives.
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Xie, Zhi-Yuan. "2-Aminopyridinium isonicotinate 2-aminopyridine." Acta Crystallographica Section E Structure Reports Online 63, no. 5 (2007): o2192—o2193. http://dx.doi.org/10.1107/s160053680701344x.

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Xiong, Hui, and Adam T. Hoye. "Mild, General, and Regioselective Synthesis of 2-Aminopyridines from Pyridine N-Oxides via N-(2-Pyridyl)pyridinium Salts." Synlett 33, no. 04 (2022): 371–75. http://dx.doi.org/10.1055/s-0040-1719865.

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AbstractA synthesis of 2-aminopyridines from pyridine N-oxides via their corresponding N-(2-pyridyl)pyridinium salts has been demonstrated and investigated. The reaction sequence features a highly regioselective conversion of the N-oxide into its pyridinium salt followed by hydrolytic decomposition of the pyridinium moiety to furnish the 2-aminopyridine product. The method is compatible with a wide range of functional groups, is scalable, and features inexpensive reagents. 15N-labeling results gave products consistent with a Zincke reaction mechanism.
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Trivedi, Mahendra Kumar, Alice Branton, Dahryn Trivedi, Gopal Nayak, Gunin Saikia, and Snehasis Jana. "Mass Spectrometry Analysis of Isotopic Abundance of 13C, 2H, or 15N in Biofield Energy Treated Aminopyridine Derivatives." American Journal of Physical Chemistry 4, no. 6 (2015): 65–70. https://doi.org/10.11648/j.ajpc.20150406.14.

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2-Aminopyridine (2-AP) and 2,6-diaminopyridine (2,6-DAP) are two derivatives of aminopyridines that act as an important organic intermediates, mostly used in medicines, dyes and organic sensors. The aim of the study was to evaluate the impact of biofield energy treatment on isotopic abundance ratios of 2H/1H, 13C/12C, or 15N/14N, in aminopyridine derivatives using gas chromatography-mass spectrometry (GC-MS). The 2-AP and 2,6-DAP samples were divided into two parts: control and treated. The control sample remained as untreated, while the treated sample was further divided into four groups as T
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Trivedi, Mahendra Kumar, Alice Branton, Dahryn Trivedi, Gopal Nayak, Gunin Saikia, and Snehasis Jana. "Mass Spectrometry Analysis of Isotopic Abundance of 13C, 2H, or 15N in Biofield Energy Treated Aminopyridine Derivatives." American Journal of Physical Chemistry 4, no. 6 (2015): 65–70. https://doi.org/10.5281/zenodo.192649.

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2-Aminopyridine (2-AP) and 2,6-diaminopyridine (2,6-DAP) are two derivatives of aminopyridines that act as an important organic intermediates, mostly used in medicines, dyes and organic sensors. The aim of the study was to evaluate the impact of biofield energy treatment on isotopic abundance ratios of 2H/1H, 13C/12C, or 15N/14N, in aminopyridine derivatives using gas chromatography-mass spectrometry (GC-MS). The 2-AP and 2,6-DAP samples were divided into two parts: control and treated. The control sample remained as untreated, while the treated sample was further divided into f
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Dissertations / Theses on the topic "2-Aminopyridine"

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Ye, Fei. "Ru- and Rh-catalyzed [2+2+2] cycloadditions : an access to fluorenone, 2-aminopyridine, and 1,3-dihydroisobenzofuran derivatives." Thesis, Paris 6, 2017. http://www.theses.fr/2017PA066347/document.

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Ce manuscrit traite de la mise au point d’une méthode d’accès éco-compatible à des squelettes carbocycliques et hétérocycliques, présents dans de nombreux composés d’intérêt biologique. Cette méthode met en œuvre une réaction de cycloaddition [2+2+2] catalysée par un métal de transition. Dans un premier temps, une voie d’accès à des fluorénones hautement substituées, ainsi qu’à des analogues a été développée. Cette voie utilise une réaction de cycloaddition [2+2+2] de diynes-[alpha, omega] pontés par un groupe benzoyle, avec des alcynes, en présence de RuCl3·nH2O. Dans un deuxième temps, des d
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Duret, Guillaume. "Synthèse de 4-aminopyridines par réaction de cycloaddition (4+2) d’ynamides." Thesis, Strasbourg, 2017. http://www.theses.fr/2017STRAF012/document.

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Les motifs de type pyridine sont des motifs centraux dans de nombreux domaines, aussi bien rencontrés dans divers principes actifs en chimie médicinale, qu’en agrochimie, chimie des matériaux et des polymères, et enfin en synthèse organique de manière générale. De nombreuses voies d'accès toujours plus simples et directes à des motifs de type pyridine polysubstituées ont été proposées dans la littérature, et, parmi ceux-ci, le motif de type aminopyridine fusionnée à retenu notre attention. En effet peu de rapports d'un tel motif sont fait dans la littérature, en partie en raison du défi synthé
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Girardeau, Elodie. "Développement et optimisation de nouvelles familles de molécules hétérocycliques ayant un intérêt commercial en tant que building blocks." Thesis, Aix-Marseille 3, 2011. http://www.theses.fr/2011AIX30030.

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Ce manuscrit décrit la synthèse et la conception de 3 nouvelles familles de molécules, les [alpha],[alpha]-diméthylamines, les 6-nitroaminopyridines et les benzimidazoles substitués. L’étude des [alpha],[alpha]-diméthylamines nous a amené à développer une voie de synthèse originale en utilisant les propriétés chimiques du chlorure de cérium, qui, lorsqu’il est complexé avec un organolithien permet d’alkyler deux fois une fonction nitrile. Une étude exhaustive des propriétés chimiques du cérium et du chlorure de cérium en synthèse organique a également été menée. La synthèse totale de la 6-nitr
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Girardeau, Elodie. "Développement et optimisation de nouvelles familles de molécules hétérocycliques ayant un intérêt commercial en tant que building blocks." Electronic Thesis or Diss., Aix-Marseille 3, 2011. http://www.theses.fr/2011AIX30030.

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Ce manuscrit décrit la synthèse et la conception de 3 nouvelles familles de molécules, les [alpha],[alpha]-diméthylamines, les 6-nitroaminopyridines et les benzimidazoles substitués. L’étude des [alpha],[alpha]-diméthylamines nous a amené à développer une voie de synthèse originale en utilisant les propriétés chimiques du chlorure de cérium, qui, lorsqu’il est complexé avec un organolithien permet d’alkyler deux fois une fonction nitrile. Une étude exhaustive des propriétés chimiques du cérium et du chlorure de cérium en synthèse organique a également été menée. La synthèse totale de la 6-nitr
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Karapanayiotis, Thanassis, G. Dimopolos-Italiano, Richard D. Bowen, and J. K. Terlouw. "Reactions of Ionised Pryridazine, 2-Aminopyrazine and 2-Aminopyridine and their a-Distonic Isomers." 2004. http://hdl.handle.net/10454/3659.

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No<br>The reactions of ionised pyridazine, aminopyrazine and aminopyridine and the corresponding ¿-distonic ions are examined by a combination of tandem mass spectrometric techniques, including analysis of metastable ion (MI), collision induced dissociation and neutralisation¿reionisation mass spectra (NRMS). Further insight into the relative stability and energy barriers towards tautomerism of each ionised heterocycle with its ¿-distonic isomer is obtained by computational methods. In all these systems, both the conventional radical-cation and the ¿-distonic tautomer are stable species which
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Tseng, Ming-Hsun, and 曾銘勳. "A Physical Study of Oligonucleotides Containing N4-(6-aminopyridin-2-yl)-2'-deoxycytidine." Thesis, 2000. http://ndltd.ncl.edu.tw/handle/54720664168624912593.

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碩士<br>中國文化大學<br>應用化學研究所<br>88<br>Oligonucleotide-directed triple helix formation is one of the most versatile methods for the sequence-specific recognition of double helical DNA. However, both sequence-specific recognition of dsDNA appears to be limited to mostly purine tracts. Design leads to expand the recognition code to pyrimidine-purine base pair (CG and AT). We have previously shown that N4-(6-aminopyridin-2-yl)-2'-deoxycytidine (P) is able to interact with the CG base pair through hydrogen bonds to form a stable P‧CG base triad. In this thesis, the oligonucleotide P1 (5'-d-TT
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Chung, Kuen-Yuan, and 鍾昆元. "A Study of Triple-stranded DNA Formation of Oligouncleotides Containing N4-(6-aminopyridin-2-yl)-2'-deoxycytidine." Thesis, 1999. http://ndltd.ncl.edu.tw/handle/04568092365709506316.

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碩士<br>中國文化大學<br>應用化學研究所<br>87<br>Oligonucleotide triple-stranded helix formation is one of the most versatile methods for the sequence-specific recognition of double helical DNA. The specificity is derived from the formation of hydrogen bonds between bases in the third strand and duplex base pairs. There are currently two classes of base triads, namely Py‧PuPy and Pu‧PuPy. Both sequence-specific recognition of dsDNA appears to be limited mostly to purine tracts. Design leads to expand the recognition code to pyrimidine-purine base pair(CG and AT). This would provide one step toward a general
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"Effets de la 4-aminopyridine sur le lymphocyte T Jurkat: Influx calcique, induction de l'apoptose et permeation d'ions /." S.l. : Universite de Sherbrooke, 2004. http://proquest.umi.com/pqdweb?did=1563018731&sid=1&Fmt=2&clientId=12520&RQT=309&VName=PQD.

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Book chapters on the topic "2-Aminopyridine"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) complex with 2-furfurylidene-2-aminopyridine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_573.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with 2-furfurylidene-2-aminopyridine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_292.

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Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of bis(2-aminopyridine)malonatocobalt(II)." 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_172.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) complex with salicylidene-2-aminopyridine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_575.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with salicylidene-2-aminopyridine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_294.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of oxalato-bridged copper(II) complex with 2-aminopyridine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 8. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-66460-5_497.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of oxalato-bridged nickel(II) complex with 2-aminopyridine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 8. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-66460-5_275.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of oxalate-bridged cobalt(II) complex with 2-aminopyridine." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 8. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-66460-5_198.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) complex with ethyl methyl ketone-2-aminopyridine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_574.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with ethyl methyl ketone-2-aminopyridine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_293.

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Conference papers on the topic "2-Aminopyridine"

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Bosenbecker, Juliano, Daniela P. Gouvêa, Geonir M. Siqueira, and Wilson Cunico. "Ultrasonics promoted synthesis of thiazolidinones from 2- aminopyridine." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013913154444.

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Salhi, Fadila, Nawel Cheikh, Didier Villemin, and Nathalie Bar. "Synthesis of 2-aminopyridine Lactones and Studies of Their Antioxidant, Antibacterial and Antifungal Properties." In ECSOC-25. MDPI, 2021. http://dx.doi.org/10.3390/ecsoc-25-11709.

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Chow, Zeta, Jeremy Johnson, Aman Chauhan, et al. "Abstract PO-014: 3-Aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP): A promising radiochemotherapy for gastroenteropancreatic neuroendocrine tumors." In Abstracts: AACR Virtual Special Conference on Radiation Science and Medicine; March 2-3, 2021. American Association for Cancer Research, 2021. http://dx.doi.org/10.1158/1557-3265.radsci21-po-014.

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Naz, Shagufta, Humaira Nadeem, sadia sarwar, Rehan Z. Paracha, Jun Q. Yu, and Fazlul Huq. "Abstract 1967: Synthesis, in vitro evaluation in ovarian cancer cells and molecular modeling analysis of novel 2-aminothiazole and 2-aminopyridine derivatives." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-1967.

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Venkatesan, G., G. Babu Anandha, and P. Ramasamy. "Synthesis and X-ray structural studies of novel metal-organic complex: Diiodobis(2-aminopyridine)cadmium(II) single crystal." In SOLID STATE PHYSICS: PROCEEDINGS OF THE 57TH DAE SOLID STATE PHYSICS SYMPOSIUM 2012. AIP, 2013. http://dx.doi.org/10.1063/1.4791322.

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Nazari, Marziyeh, Stephen F. Collins, Matthew R. Hill, and Mikel C. Duke. "MOF-Coated Optical Fiber Sensor for Detection of 4-Aminopyridine in Water." In Optical Sensors. OSA, 2018. http://dx.doi.org/10.1364/sensors.2018.sem4e.2.

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Srishailam, K., and G. Rao. "SYNTHESIS, MOLECULAR STRUCTURE, VIBRATIONAL CHARACTERISTICS, PROFILES OF OTHER MOLECULAR PROPERTIES AND ANTICANCER ACTIVITY OF 2-((2-AMINOPYRIDIN-3-YL)METHYLENE)-N-PHENYLHYDRAZINECARBOTHIOAMIDE AS PROVIDED BY SPECTROSCOPIC AND DFT INVESTIGATIONS." In 2023 International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2023. http://dx.doi.org/10.15278/isms.2023.6689.

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