Relevant bibliographies by topics / Thiophene synthesis

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Thiophene synthesis'

Author: Grafiati
Published: 4 June 2021
Last updated: 10 February 2022

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Journal articles on the topic "Thiophene synthesis"

1

Duc, Dau Xuan. "Recent Progress in the Synthesis of Benzo[b]thiophene." Current Organic Chemistry 24, no. 19 (2020): 2256–71. http://dx.doi.org/10.2174/1385272824999200820151545.

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: Benzo[b]thiophenes are aromatic heterocyclic compounds containing benzene and thiophene rings. This class of heterocycles is present in a large number of natural and non-natural compounds. Benzo[b]thiophene derivatives have a broad range of applications in medicinal chemistry such as antimicrobial, anticancer, antioxidant, anti-HIV and antiinflammatory activities. The use of benzo[b]thiophene derivatives in other fields has also been reported. Various benzo[b]thiophenes compounds have been employed as organic photoelectric materials, while several benzo[b]thiophenes have been used as organic
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Clark, Peter D., Nicholas M. Irvine, and Pratibha Sarkar. "The synthesis of 3H-naphthol[1,8-bc]thiophene derivatives." Canadian Journal of Chemistry 69, no. 6 (1991): 1011–16. http://dx.doi.org/10.1139/v91-148.

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Methods for the synthesis of keto derivatives of the little studied naphtho[1,8-bc]thiophene system have been developed. Using the readily available benzothiophene derivative 6,7-dihydrobenzo[b]thiophen-4(5H)-one 4, a 3-keto-naphtho[1,8-bc]thiophene 14 was synthesized by a tin(IV) chloride catalyzed cyclization of the acid chloride derivative of the saturated acid 13b. The bicyclic ketone 4 was also used to prepare the keto-sulfoxide 7, which was cyclized to the 4-keto-naphtho[1,8-bc]thiophene system 9 in a Pummerer-type rearrangement. Key words: synthesis, organosulfur, naphtho[1,8-bc]thiophe
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3

Vu Quoc, Trung, Duong Tran Thi Thuy, Thuan Dang Thanh, et al. "Some chalcones derived from thiophene-3-carbaldehyde: synthesis and crystal structures." Acta Crystallographica Section E Crystallographic Communications 75, no. 7 (2019): 957–63. http://dx.doi.org/10.1107/s2056989019007503.

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The synthesis, spectroscopic data and crystal and molecular structures of four 3-(3-phenylprop-1-ene-3-one-1-yl)thiophene derivatives, namely 1-(4-hydroxyphenyl)-3-(thiophen-3-yl)prop-1-en-3-one, C13H10O2S, (1), 1-(4-methoxyphenyl)-3-(thiophen-3-yl)prop-1-en-3-one, C14H12O2S, (2), 1-(4-ethoxyphenyl)-3-(thiophen-3-yl)prop-1-en-3-one, C15H14O2S, (3), and 1-(4-bromophenyl)-3-(thiophen-3-yl)prop-1-en-3-one, C13H9BrOS, (4), are described. The four chalcones have been synthesized by reaction of thiophene-3-carbaldehyde with an acetophenone derivative in an absolute ethanol solution containing potass
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4

Zhou, Yue, Jie Hao, and Dongbing Zhao. "Divergent synthesis of 3-substituted thieno[3,4-b]thiophene derivatives via hydroxy-based transformations." Materials Chemistry Frontiers 3, no. 7 (2019): 1422–26. http://dx.doi.org/10.1039/c9qm00128j.

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Modular assembly of 3-substituted thieno[3,4-b]thiophenes: we have developed the first Pd-catalytic method to access 3-hydroxythieno[3,4-b]thiophene-2-carboxylate, which can be widely utilized for modular assembly of structurally diverse 3-substituted thieno[3,4-b]thiophene derivatives.
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Irgashev, Roman A., Nadezhda S. Demina, and Gennady L. Rusinov. "Construction of 2,3-disubstituted benzo[b]thieno[2,3-d]thiophenes and benzo[4,5]selenopheno[3,2-b]thiophenes using the Fiesselmann thiophene synthesis." Organic & Biomolecular Chemistry 18, no. 16 (2020): 3164–68. http://dx.doi.org/10.1039/d0ob00300j.

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Bolduc, Andréanne, Stéphane Dufresne, Garry S. Hanan, and W. G. Skene. "Synthesis, photophysics, and electrochemistry of thiophene–pyridine and thiophene–pyrimidine dyad comonomers." Canadian Journal of Chemistry 88, no. 3 (2010): 236–46. http://dx.doi.org/10.1139/v09-166.

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A series of new π-conjugated donor (D) and acceptor (A) dyad comonomers were prepared using Suzuki coupling protocols. The D–A comonomers consisting of thiophene/bithiophene as donors and pyridine/pyrimidine as acceptors were prepared to investigate their photophysical and electrochemical properties. The dyads were spectroscopically confirmed to be highly conjugated. This was further supported by the X-ray crystal structure of the bithophene–pyridine dyad that showed all the heterocycles to be coplanar. It was further found that the fluorescence yields (Φfl) of the dyads were highly dependent
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Damit, E. F., N. Nordin, A. Ariffin, and K. Sulaiman. "Synthesis of Novel Derivatives of Carbazole-Thiophene, Their Electronic Properties, and Computational Studies." Journal of Chemistry 2016 (2016): 1–14. http://dx.doi.org/10.1155/2016/9360230.

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A series of carbazole-thiophene dimers,P1–P9, were synthesized using Suzuki-Miyaura and Ullmann coupling reactions. InP1–P9, carbazole-thiophenes were linked at the N-9 position for different core groups via biphenyl, dimethylbiphenyl, and phenyl. Electronic properties were evaluated by UV-Vis, cyclic voltammogram, and theoretical calculations. Particularly, the effects of conjugation connectivity on photophysical and electrochemical properties, as well as the correlation between carbazole-thiophene and the core, were studied. Carbazole connecting with thiophenes at the 3,6-positions and the p
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Demina, Nadezhda S., Nikita A. Kazin, Nikolay A. Rasputin, Roman A. Irgashev, and Gennady L. Rusinov. "Synthesis of aryl-substituted thieno[3,2-b]thiophene derivatives and their use for N,S-heterotetracene construction." Beilstein Journal of Organic Chemistry 15 (November 12, 2019): 2678–83. http://dx.doi.org/10.3762/bjoc.15.261.

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Fiesselmann thiophene synthesis was applied for the convenient construction of thieno[3,2-b]thiophene derivatives. Thus, new 5- or 6-aryl-3-hydroxythieno[3,2-b]thiophene-2-carboxylates were obtained by condensation of 5- or 4-aryl-3-chlorothiophene-2-carboxylates, respectively, with methyl thioglycolate in the presence of potassium tert-butoxide. The saponification of the resulting esters, with decarboxylation of the intermediating acids, gave the corresponding thieno[3,2-b]thiophen-3(2H)-ones. The latter ketones were used to synthesize new N,S-heterotetracenes, namely 9H-thieno[2',3':4,5]thie
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Madabhushi, Sridhar, Srinivas Kurva, Vinodkumar Sriramoju, Jagadeesh Babu Nanubolu та Suresh Reddy Cirandur. "Efficient synthesis of polyfunctionalized thiophene-2,3-diones and thiophen-3(2H)-ones using β-oxodithioesters". RSC Advances 5, № 79 (2015): 64797–801. http://dx.doi.org/10.1039/c5ra11629e.

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Ilhan, Koray T., Sebahat Topal, Mehmet S. Eroglu, and Turan Ozturk. "Concise synthesis of 3-alkylthieno[3,2-b]thiophenes; building blocks for organic electronic and optoelectronic materials." RSC Advances 9, no. 66 (2019): 38407–13. http://dx.doi.org/10.1039/c9ra08023f.

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Four step synthesis of 3-alkylthieno[3,2-b]thiophenes in the literature was reduced to two steps in good yields, through the preparation of the mono ketone, i.e. 1-(thiophene-3-ylthio)alkan-2-one, from 3-bromothiophene and ring formation reaction.
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Dissertations / Theses on the topic "Thiophene synthesis"

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Kiriy, Nataliya. "Thiophene Based Semiconductors: Synthesis and Characterizations." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2006. http://nbn-resolving.de/urn:nbn:de:swb:14-1141840200043-85237.

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Diverse conformational transitions and aggregations of regioregular head-to-tail polyhexylthiophene in different environments have been studied by means of AFM and UV-vis spectroscopy. A helical conformation of the main chain with 12 thiophenes rings per each helical turn has been proposed. Length of the particles varies from several nanometers to several hundreds nanometers and can be adjusted by the solvents composition or concentration of PATs. Such well-defined organic semiconductor 1D particles can be used as building blocks for future nanoscale and molecular level electronic devices. Oli
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Kiriy, Nataliya. "Thiophene Based Semiconductors: Synthesis and Characterizations." Doctoral thesis, Technische Universität Dresden, 2005. https://tud.qucosa.de/id/qucosa%3A24675.

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Diverse conformational transitions and aggregations of regioregular head-to-tail polyhexylthiophene in different environments have been studied by means of AFM and UV-vis spectroscopy. A helical conformation of the main chain with 12 thiophenes rings per each helical turn has been proposed. Length of the particles varies from several nanometers to several hundreds nanometers and can be adjusted by the solvents composition or concentration of PATs. Such well-defined organic semiconductor 1D particles can be used as building blocks for future nanoscale and molecular level electronic devices. Oli
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Unur, Ece. "Synthesis Of Thiophene Capped Polytetrahydrofuran Conducting Copolymers." Master's thesis, METU, 2003. http://etd.lib.metu.edu.tr/upload/4/1144625/index.pdf.

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Living polytetrahydrofuran (PTHF) was terminated with sodium thiophenemethonate to yield a polymer with thiophene groups at one (PTHF1) and both ends (PTHF2). Copolymerizations of PTHF1 and PTHF2 insulating polymers with pyrrole and thiophene were achieved in water-p-toluene sulfonic acid (PTSA) and acetonitrile (AN)-tetrabutylammonium tetrafluoroborate (TBAFB) solvent-electrolyte couples via constant potential electrolysis. Characterization of the samples were performed by Nuclear Magnetic Resonance Spectroscopy (NMR), cyclic voltammetry (CV), Fourier Transform Infrared Spectroscopy (FT-IR),
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Landman, Marile. "Synthesis of metal complexes with thiophene ligands." Thesis, Access to E-Thesis, 2000. http://upetd.up.ac.za/thesis/available/etd-12042006-143722/.

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Sousa, Paula T. de. "The synthesis of novel thiophene analogues of leukotrienes." Thesis, University of East Anglia, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317613.

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Gledhill, Adrian Paul. "Synthesis of polysubstituted fatty acids via thiophene intermediates." Thesis, Nottingham Trent University, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.304892.

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Weddell, Derek Alexander. "Synthesis, structure determination and mechanism in thiophene derivatives." Thesis, Nottingham Trent University, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.343542.

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Van, Jaarsveld Nina Alletta. "Synthesis and structure of modified thiophene biscarbene complexes." Diss., University of Pretoria, 2010. http://hdl.handle.net/2263/23311.

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Waugaman, Marlene. "Synthesis and characterization of 3-[Oligo(dimethylsiloxane] thiophene macromonomers." DigitalCommons@Robert W. Woodruff Library, Atlanta University Center, 1998. http://digitalcommons.auctr.edu/dissertations/1293.

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Electronic conductive polymers such as polyacetylenes, polyanilines and polythiophenes, are not easy to process due to lack of tractability and solubility. Chemical modifications of the polythiophenes backbone have been utilized to improve the processibility. Our goal is to synthesize and characterize 3-[oligo(dimethylsiloxane)]- thiophene macromonomers as precursors for potentially processible, conductive derivatives of polythiophene. The precursor will be used in the preparation of various poly {[3- oligo(dimethylsiloxane)]thiophene-co-3-methylthiophene} random copolymers. By increasing the
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Thatti, Ravtej Singh. "The synthesis and properties of phenyl-cored thiophene dendrimers." Thesis, Kingston University, 2016. http://eprints.kingston.ac.uk/37349/.

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Dendrimers are globular macromolecules that have a range of applications. These nonnally exploit the individual prope1ties of the functional groups that make up the overall dendrimer. The polyvalent properties of dendrimers are widely used in biomedical scaffolds and catalysis. The internal cavities with the structure can also be harnessed for encapsulation. This application has evoked interest especially within the bio-medical field, using dendrimers as host molecules to increase the solubility of drug molecules. In this research, a set of dendrimers were prepared to test the potential of enc
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Books on the topic "Thiophene synthesis"

1

F, Perepichka Dmitrii, ed. Handbook of thiophene-based materials. Wiley, 2009.

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Sousa, Paulo T. De. The synthesis of novel thiophene analogues of leukotrienes. University of East Anglia, 1992.

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3

Gronowitz, Salo, and Anna-Britta Hörnfeldt. Thiophenes (Best Synthetic Methods). Academic Press, 2004.

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Gronowitz, Salo, and Anna-Britta Hörnfeldt. Thiophenes (Best Synthetic Methods). Academic Press, 2004.

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O'Donovan, Allison R. M. The synthesis and reactions of silylated thiophenes and their dioxides. 1997.

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Book chapters on the topic "Thiophene synthesis"

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Li, Jie Jack. "Paal thiophene synthesis." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_187.

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Li, Jie Jack. "Fiesselmann thiophene synthesis." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_97.

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Li, Jie Jack. "Fiesselmann thiophene synthesis." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_104.

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Li, Jie Jack. "Paal thiophene synthesis." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_200.

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Li, Jie Jack. "Hinsberg synthesis of thiophene derivatives." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_125.

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Majumdar, Krishna C., and Shovan Mondal. "Thiophene and Other Sulfur Heterocycles." In Heterocycles in Natural Product Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527634880.ch11.

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Siekierski, M., J. Plocharski, M. Catellani, and S. Destri. "Electrochemical Synthesis of Poly(dithieno thiophene)." In Electronic Properties of Polymers. Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-84705-9_62.

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Livi, Francesco, Jon E. Carlé, and Eva Bundgaard. "Thiophene in Conducting Polymers: Synthesis of Poly(thiophene)s and Other Conjugated Polymers Containing Thiophenes, for Application in Polymer Solar Cells." In Topics in Heterocyclic Chemistry. Springer International Publishing, 2014. http://dx.doi.org/10.1007/7081_2014_128.

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Abraham, Ann, J. J. McGuire, J. Galivan, B. Rao Vishnuvajjala, and M. G. Nair. "New Thiophene Substituted 10-Deazaaminopterins: Synthesis and Biological Evaluation." In Advances in Experimental Medicine and Biology. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-2960-6_84.

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Bridges, C. R., and D. S. Seferos. "Chapter 2. Controlled Chain-growth Synthesis of Conjugated Polymers: Moving Beyond Thiophene." In Polymer Chemistry Series. Royal Society of Chemistry, 2016. http://dx.doi.org/10.1039/9781782624004-00038.

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Conference papers on the topic "Thiophene synthesis"

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Carvalho, Diego B., Camila B. Andrade, Carla R. Z. Miranda, et al. "Synthesis of Thiophene Acetylenes via Sonogashira Cross- Coupling Reactions." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013820103940.

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Thomae, D., G. Kirsch, and P. Seck. "Synthesis of Thiophene Analogues of the Tacrine Series." In The 10th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2006. http://dx.doi.org/10.3390/ecsoc-10-01380.

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MOURA, R. O., R. S. A. DE ARAÚJO, F. F. RIBEIRO, et al. "Synthesis and Citotoxicity Evaluation of 3-Cyano-2-aminocycloalkyl[ b]thiophene derivatives." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0288-2.

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Jaekle, Frieder, Kshitij Parab, and Anand Sundararaman. "Synthesis and Photophysical Characterization of Boron-Modified Thiophene Polymers." In Organic Photonics and Electronics. OSA, 2006. http://dx.doi.org/10.1364/ope.2006.opmb3.

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Destri, S., M. Mascherpa, and W. Porzio. "Synthesis and characterizatios of new thiophene phenylene based polyazomethines." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835251.

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Tichý, Michal, and Michal Hocek. "Synthesis and biological activity of thiophene fused 7-deazapurine ribonucleosides." In XVIth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2014. http://dx.doi.org/10.1135/css201414385.

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Dey, Somnath, Yang Han, Siham Y. Al-Qaradawi, Hassan S. Bazzi, Martin Heeney, and Mohammed Al-Hashimi. "Synthesis and Characterization of Soluble Thiophene-, Selenophene- and Tellurophene-Vinylene Copolymers." In Qatar Foundation Annual Research Conference Proceedings. Hamad bin Khalifa University Press (HBKU Press), 2016. http://dx.doi.org/10.5339/qfarc.2016.eepp1934.

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Romero-Parra, Javier, Hernán Pessoa-Mahana, and C. David Pessoa-Mahana. "Benzo[b]thiophene dimerization: A promising experimental finding directed to the C-3 functionalization with aryl alcohols." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013105155647.

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Blanco, José, Paula Abeijón, Olga Caamaño, Franco Fernández, Marcos García, and Xerardo García-Mera. "A convenient synthesis of new 6-substituted purinylcarbanucleosides on cyclopenta[b]thiophene." In The 12th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01238.

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Tadjarodi, Azadeh, and Saeedeh Eslami Nezhad. "Microwave-assisted solvent-free synthesis of Thiocarbamic acid [(thiophene-2-yl) ethylidene]hydrazide." In The 13th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00157.

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Reports on the topic "Thiophene synthesis"

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Allcock, Harry R., Jeffrey A. Dodge, Leon S. Van Dyke, and Charles R. Martin. Polyphosphazenes Bearing Polymerizable Pyrrole, Thiophene and Furan Side Groups: Synthesis and Chemical Oxidation. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada249747.

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Synthesis of 6-Methyl-9-n-propyldibenzo thiophene-4-ol ammended to 6-Methyl-9-(1-methylethyl)-dibenzo thiophene-4-ol. Quarterly technical progress report No. 6, October 28, 1991--January 26, 1992. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/10158452.

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