Academic literature on the topic '2-aminothiophenes'

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Journal articles on the topic "2-aminothiophenes"

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Kirsch, Gilbert, Ahmed Abdelwahab, and Atef Hanna. "Targeted Synthesis of 4-Chloro-3-formylthieno[2,3-b]pyridine and/or 4-Chlorothieno[2,3-b]pyridine by Reaction between N-Protected 3-Acetyl-2-aminothiophenes and Vilsmeier–Haack Reagent." Synthesis 49, no. 13 (2017): 2971–79. http://dx.doi.org/10.1055/s-0036-1588992.

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Formylated chlorothieno[2,3-b]pyridine derivatives were synthesized by reaction between N-protected 3-acetyl-2-aminothiophenes and Vilsmeier–Haack reagent under classical conditions. These products were not accessible without N-protection of the starting materials or by reaction between the reagent and 4-chlorothieno[2,3-b]pyridine under any conditions. The conditions of the reaction could be altered to produce unformylated derivatives in better yields than reaction with unprotected aminothiophene.
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Terrier, François, Marie-José Pouet, Khalid Gzouli, Jean-Claude Hallé, Francis Outurquin, and Claude Paulmier. "Carbon-carbon coupling of 4,6-dinitrobenzofuroxan with 3-aminothiophenes: a kinetic and structural study." Canadian Journal of Chemistry 76, no. 6 (1998): 937–45. http://dx.doi.org/10.1139/v98-079.

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Potentiometric measurements carried out in a 50-50 (v/v) H2O-Me2SO mixture together with 1H and 13C NMR studies carried out in pure Me2SO-d6 reveal that 3-aminothiophene (4a), 3-N-(methylamino)thiophene (4b), and 3-N,N-dimethylaminothiophene (4c) undergo protonation exclusively at the amino groups in dilute acid solutions. The pKa values of 4a, 4b, and 4c are equal to 3.38, 3.65, and 3.53, respectively, at 25°C, comparing well with those for related anilines in the same aqueous Me2SO mixtures. However, despite this similarity of the nitrogen basicities, compounds 4a, 4b, and 4c are found to be
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Sabnis, R. W., D. W. Rangnekar, and N. D. Sonawane. "2-aminothiophenes by the gewald reaction." Journal of Heterocyclic Chemistry 36, no. 2 (1999): 333–45. http://dx.doi.org/10.1002/jhet.5570360203.

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Hallas, Geoffrey, and Andrew D. Towns. "Dyes derived from aminothiophenes—Part 2. Spectroscepic properties of some disperse dyes derived from 2-aminothiophenes." Dyes and Pigments 33, no. 3 (1997): 205–13. http://dx.doi.org/10.1016/s0143-7208(96)00047-2.

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Zeng, Fanxun, Pengjian Liu, Xusheng Shao, Zhong Li, and Xiaoyong Xu. "Catalyst-free and selective synthesis of 2-aminothiophenes and 2-amino-4,5-dihydrothiophenes from 4-thiazolidinones in water." RSC Advances 6, no. 64 (2016): 59808–15. http://dx.doi.org/10.1039/c6ra11151c.

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Virieux, David, Anne-Françoise Guillouzic, and Henri-Jean Cristau. "Triphenylphosphine catalyzed formation of functionalized 2-aminothiophenes." Heteroatom Chemistry 18, no. 3 (2007): 312–15. http://dx.doi.org/10.1002/hc.20300.

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Thanna, Sandeep, Susan E. Knudson, Anna Grzegorzewicz, et al. "Synthesis and evaluation of new 2-aminothiophenes against Mycobacterium tuberculosis." Organic & Biomolecular Chemistry 14, no. 25 (2016): 6119–33. http://dx.doi.org/10.1039/c6ob00821f.

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Sridhar, Madabhushi, Rayankula Mallikarjuna Rao, Nanduri H. K. Baba, and Ravindra M. Kumbhare. "Microwave accelerated Gewald reaction: synthesis of 2-aminothiophenes." Tetrahedron Letters 48, no. 18 (2007): 3171–72. http://dx.doi.org/10.1016/j.tetlet.2007.03.052.

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Sabnis, R. W., D. W. Rangnekar, and N. D. Sonawane. "ChemInform Abstract: 2-Aminothiophenes by the Gewald Reaction." ChemInform 30, no. 36 (2010): no. http://dx.doi.org/10.1002/chin.199936290.

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Zhang, Xuxue, Chuan Liu, Yupian Deng та Song Cao. "Chemo- and regioselective synthesis of polysubstituted 2-aminothiophenes by the cyclization of gem-dibromo or gem-dichloroalkenes with β-keto tertiary thioamides". Organic & Biomolecular Chemistry 18, № 38 (2020): 7540–44. http://dx.doi.org/10.1039/d0ob01821j.

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A facile and practical method for the synthesis of 2,3,4-trisubstituted 2-aminothiophenes by the cyclization of gem-dibromoalkenes or gem-dichloroalkenes with β-keto tertiary thioamides has been developed.
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Dissertations / Theses on the topic "2-aminothiophenes"

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Mahmoud, Ahmed B. Abdelwahab. "Synthesis and reactivity of 3-acetyl-2-aminothiophenes." Thesis, Université de Lorraine, 2016. http://www.theses.fr/2016LORR0318/document.

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Un intérêt grandissant pour le système thiéno[2,3-b] pyridine est apparu ces trois dernières décennies. De nombreux chercheurs ont présentés des composés basés sur ce système comme traitement possible de l'anxiété et de la dépression, comme bactéricide, contre l'inflammation et la leishmania, la malaria et les maladies auto-immunes. Les ortho-amino acyl thiophènes sont des produits de départ possible pour synthétiser ces motifs. L'accès à ce type de composés sera la première étape de ce travail. Nous décrivons ici la première synthèse de 3-acétyl-2-aminothiophènes en utilisant la réaction à 3
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Cruz, Rayssa Marques Duarte da. "Síntese de novos derivados 2-aminotiofênicos através da reação de Gewald utilizando produtos naturais como precursores." Universidade Federal da Paraíba, 2015. http://tede.biblioteca.ufpb.br:8080/handle/tede/8822.

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Submitted by Cristhiane Guerra (cristhiane.guerra@gmail.com) on 2017-02-03T14:55:00Z No. of bitstreams: 1 arquivototal.pdf: 1708717 bytes, checksum: 2d354a04512a631331c735eca33744f1 (MD5)<br>Made available in DSpace on 2017-02-03T14:55:00Z (GMT). No. of bitstreams: 1 arquivototal.pdf: 1708717 bytes, checksum: 2d354a04512a631331c735eca33744f1 (MD5) Previous issue date: 2015-03-26<br>Conselho Nacional de Pesquisa e Desenvolvimento Científico e Tecnológico - CNPq<br>Natural products represent a vast source of molecules with pharmacological potential and serve as a basis for seeking and obtainin
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Langille, Adrienne. "Synthesis and biological evaluation of 2- aminothiophene and benzothiazole derivatives as isoprenoid biosynthesis inhibitors." Thesis, McGill University, 2013. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=117127.

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The condensation of stable 2-(1-(trimethylsilyl)ethylidene)malononitrile with elemental sulfur was explored in the parallel-synthesis of a small library of structurallydiverse2-aminothiophenesandthieno[2,3-d]pyrimidines. Bromination and ipso-iododesilylation of these heterocyclic scaffolds provided synthetic methods to efficiently generate key intermediates, allowing for great versatility. Bisphosphonic acid derivatives of thieno[2,3-d]pyrimidine and benzothiazole scaffolds, with favourable physicochemical properties, were evaluated for their ability to inhibit isoprenoid biosynthesis and pote
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Schumann, Jörg. "Arylsubstituierte Fünfringheteroaromaten als Halbleiter- und Emittermaterialien zur Anwendung in Organischen Elektrolumineszenzdioden." Doctoral thesis, Technische Universitaet Bergakademie Freiberg Universitaetsbibliothek &quot;Georgius Agricola&quot, 2009. http://nbn-resolving.de/urn:nbn:de:swb:105-2623887.

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Zur Herstellung Organischer Leuchtdioden (OLED) auf der Basis kleiner Moleküle werden geeignete Verbindungen als Ladungstransport- und Emittermaterialien benötigt. Die Arbeit beschreibt die Darstellung heteroaromatischer Triarylamine durch Ringschlussreaktion. Ausgehend von N,N-diarylsubstituierten Thioharnstoffen und -Thiocarbonsäureamiden sowie von geeigneten 2-Halogencarbonylverbindungen wurden arylsubstituierte 2-Aminothiazole und 2-Aminothiophene dargestellt. Durch den Einsatz von bifunktionellen Edukten erhält man so auch 5,5´-verknüpfte, 4,4´-verknüpfte und aminoverknüpfte Hetarensystem
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Liang, Min-Chieh, та 梁閔傑. "(I)A Combined Tamaru Allylation/Olefin Cross-Metathesis Approach for the Total Syntheses of (±)-Paniculidine C and 2-Methylcarbazole and (II)Temperature-Controlled Thiation of α-Cyano-β-Alkynyl Carbonyl Derivatives for De Novo Synthesis of 2-Aminothiophenes and Thieno[2,3-c]isothiazoles". Thesis, 2018. http://ndltd.ncl.edu.tw/handle/7gd757.

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碩士<br>國立交通大學<br>應用化學系碩博士班<br>107<br>This dissertation is divided into two parts: The first chapter describes the synthesis of 2-methylcarbazole from the commercial available indole through a series of reactions comprising a Tamaru allylation, an olefin cross metathesis and an auto-oxidative Friedel-Crafts cyclization. This experiment suggests a possible biosynthetic link between 3-prenylated indoles and 2-methylcarbazole alkaloids. Moreover, we explored the optimization of cross metathesis reactions between 3-allylindole and various protected allyl alcohols. The second chapter describes a no
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Schumann, Jörg. "Arylsubstituierte Fünfringheteroaromaten als Halbleiter- und Emittermaterialien zur Anwendung in Organischen Elektrolumineszenzdioden." Doctoral thesis, 2001. https://tubaf.qucosa.de/id/qucosa%3A22388.

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Zur Herstellung Organischer Leuchtdioden (OLED) auf der Basis kleiner Moleküle werden geeignete Verbindungen als Ladungstransport- und Emittermaterialien benötigt. Die Arbeit beschreibt die Darstellung heteroaromatischer Triarylamine durch Ringschlussreaktion. Ausgehend von N,N-diarylsubstituierten Thioharnstoffen und -Thiocarbonsäureamiden sowie von geeigneten 2-Halogencarbonylverbindungen wurden arylsubstituierte 2-Aminothiazole und 2-Aminothiophene dargestellt. Durch den Einsatz von bifunktionellen Edukten erhält man so auch 5,5´-verknüpfte, 4,4´-verknüpfte und aminoverknüpfte Hetarensystem
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Books on the topic "2-aminothiophenes"

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Litvinov, Viktor P. Cyclization of Nitriles As Synthetic Route to 2- and 3-Aminothiophenes. Routledge, 1986.

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Conference papers on the topic "2-aminothiophenes"

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Ould M'hamed, Mohamed, and Saad Al Qahtani. "Green and efficient technique for the three component synthesis of 2-aminothiophenes using ball-milling method through Gewald reaction." In The 20th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a050.

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Khachatryan, D. S., A. V. Kolotaev, V. N. Osipov, V. A. Yashkir, and K. R. Matevosyan. "Quaternary ammonium derivatives of 2-aminothiophene-3-carboxylates with antimicrobial activity." In PROCEEDINGS OF THE 3RD INTERNATIONAL CONFERENCE ON AUTOMOTIVE INNOVATION GREEN ENERGY VEHICLE: AIGEV 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5087355.

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