Relevant bibliographies by topics / 2-c]thiazoles

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic '2-c]thiazoles'

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

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Journal articles on the topic "2-c]thiazoles"

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Liu, Wei, Xin Yu, and Chunxiang Kuang. "Palladium-Catalyzed C-2 Selective Olefination of Thiazoles." Organic Letters 16, no. 6 (2014): 1798–801. http://dx.doi.org/10.1021/ol500542j.

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2

Shaaban, Khaled A., Mohamed Shaaban, Hafizur Rahman, et al. "Karamomycins A–C: 2-Naphthalen-2-yl-thiazoles from Nonomuraea endophytica." Journal of Natural Products 82, no. 4 (2019): 870–77. http://dx.doi.org/10.1021/acs.jnatprod.8b00928.

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3

Gogoi, Prasanta, Bappi Paul, Sukanya Hazarika, and Pranjit Barman. "Gold nanoparticle catalyzed intramolecular C–S bond formation/C–H bond functionalization/cyclization cascades." RSC Advances 5, no. 71 (2015): 57433–36. http://dx.doi.org/10.1039/c5ra10885c.

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An efficient synthesis of 2-(N-aryl)aminobenzo[d]-1,3-thiazoles via intramolecular C–S bond formation/C–H bond functionalization utilizing an unusual cocatalytic Au-NPs/KMnO<sub>4</sub> system under an oxygen atmosphere at 80 °C is presented.
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4

Shailendra, Tiwari, and Nizamuddin. "Synthesis and fungicidal activities of some 2-substituted arylamino-5-(2' -furyl)- 1,3,4-thiadiazolo[3,2-c]thiazoles and 5-substituted aryl-2-substituted arylamino-1 ,3 ,4-thiadiazolo [3 ,2-c ]thiazoles." Journal of Indian Chemical Society Vol. 90, May 2013 (2013): 679–83. https://doi.org/10.5281/zenodo.5772308.

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Department of Chemistry, University of Allahabad, Allahabad-211 002, Uttar Pradesh, India <em>E-mail</em> : drshailendratiwariau@gmail. com Department of Chemistry, DDU Gorakhpur University, Gorakhpur-273 009, Uttar Pradesh, India <em>E-mail</em> : prnukhan@gmail.com <em>Manuscript received 13 December 2011, revised 14 May 2012, accepted 11 July 2012</em> Several 2-substituted arylamino-5-(2<em>&#39;</em>-furyl)-1,3,4-thiadiazolo[3,2-c]thiazoles have been synthesised by cyclisation of 3-substituted aryl thiocarbanilido-2-(2<em>&#39;</em> -furyl)thiazolidin-4-ones with conc. H<sub>2</sub>SO<sub
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5

Liu, Wei, Xin Yu, and Chunxiang Kuang. "ChemInform Abstract: Palladium-Catalyzed C-2 Selective Olefination of Thiazoles." ChemInform 45, no. 37 (2014): no. http://dx.doi.org/10.1002/chin.201437148.

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6

Yan, Kelu, Daoshan Yang, Wei Wei, Pengfei Sun, Yunxiang Lu, and Hua Wang. "A copper-catalyzed cascade reaction of o-bromoarylisothiocyanates with isocyanides leading to benzo[d]imidazo[5,1-b]thiazoles under ligand-free conditions." Organic Chemistry Frontiers 3, no. 5 (2016): 556–60. http://dx.doi.org/10.1039/c6qo00030d.

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Nedolya, Nina, Boris Trofimov, Olga Tarasova, and Alexander Albanov. "tert-Butoxide-Assisted Structural Transformation of 2-Aza-1,3,5-trienes: Fast Track to 5-Ethynyl-2-vinyl- and 2,5-Divinyl-1,3-thiazoles." Synthesis 50, no. 21 (2018): 4313–24. http://dx.doi.org/10.1055/s-0037-1609561.

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Treatment of 2-aza-1,3,5-trienes, methyl N-[2-alkoxy-1-(prop-2-ynylsulfanyl)buta-1,3-dienyl]- and methyl N-[1-(allylsulfanyl)-2-alkoxybuta-1,3-dienyl]iminoformates, which are easily obtained from lithiated alkoxyallenes, methoxymethyl isothiocyanate, and propargyl or allyl bromide, with t-BuOK or t-BuONa in DMSO–THF results in the formation of 5-ethynyl-2-vinyl- and 2,5-divinyl-1,3-thiazoles. The reactions are realized under mild conditions at ca. –30 °C for 30 minutes. An unprecedented structural transformation of the (prop-2-ynylsulfanyl)- and (allylsulfanyl)-substituted 2-aza-1,3,5-trienes
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8

Luo, Puying, Qiuping Ding, Yuanyuan Ping, and Jianan Hu. "Regioselective ortho-trifluoromethylthiolation of 2-arylbenzo[d]thiazole via tandem substrate-assisted C–H iodination and trifluoromethylthiolation." Organic & Biomolecular Chemistry 14, no. 10 (2016): 2924–29. http://dx.doi.org/10.1039/c6ob00005c.

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A mild and efficient tandem benzo[d]thiazole directed C–H iodination and trifluoromethylthiolation for the synthesis ofortho-trifluoromethylthiolated 2-arylbenzo[d]thiazoles have been developed using AgSCF<sub>3</sub>as a coupling partner.
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9

Zi, You, Konrad Wagner, Fritz Schömberg, and Ivan Vilotijevic. "Selective C–H chalcogenation of thiazoles via thiazol-2-yl-phosphonium salts." Organic & Biomolecular Chemistry 18, no. 27 (2020): 5183–91. http://dx.doi.org/10.1039/d0ob00684j.

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Medicinally relevant substituted benzothiazoles and thiazoles are prepared under mild conditions by a regioselective C2–H chalcogenation via preparation of the phosphonium salt and the subsequent reaction with S- and Se-centered nucleophiles.
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10

Shaik, Siddiq Pasha, Faria Sultana, A. Ravikumar, Satish Sunkari, Abdullah Alarifi, and Ahmed Kamal. "Regioselective oxidative cross-coupling of benzo[d]imidazo[2,1-b]thiazoles with styrenes: a novel route to C3-dicarbonylation." Organic & Biomolecular Chemistry 15, no. 36 (2017): 7696–704. http://dx.doi.org/10.1039/c7ob01778b.

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Iodine promoted metal-free domino protocol has been developed for the C3-dicarbonylation of benzo[d]imidazo[2,1-b]thiazoles (IBTs) with styrenes via oxidative cleavage of the C(sp<sup>2</sup>)–H bond, followed by C3-nucleophilic attack of IBT and oxidation.
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Dissertations / Theses on the topic "2-c]thiazoles"

1

Richter, Frank. "Development of the Solution-Spray Flash-Vacuum-Pyrolysis Technique in the Synthesis of Allenyl Isothiocyanates and Synthesis of Complex 2-Amino-1,3-thiazole Derivatives." Doctoral thesis, Universitätsbibliothek Chemnitz, 2015. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-175339.

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Gas-phase thermolysis is a long-known and well established method for the preparation of reactive species. It is, however, limited to relatively volatile substances, which are easily vaporised. In the present work, the solution-spray technique for preparative scale was developed. With this technique, it is possible to subject low-volatile substances, which hardly vaporise even under high-vacuum conditions, to gas-phase thermolysis. By utilising oil nozzles used in heating and burner systems, it was possible to integrate a stable solution-spray into the existing flash-vacuum-pyrolysis system. T
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Book chapters on the topic "2-c]thiazoles"

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Lozano, Erika, Melissa M. Lewis-Bakker, and Lakshmi P. Kotra. "Synthetic Strategies and Biological Activities of 1,5-Disubstituted Pyrazoles and 2,5-Disubstituted Thiazoles." In Strategies Towards the Synthesis of Heterocycles and Their Applications [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.108923.

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Pyrazoles and thiazoles belong to 5-membered aromatic heterocycles called azoles. In addition to a nitrogen, pyrazoles contain an additional nitrogen in a 1,2 linkage and thiazoles contain a sulfur atom in a 1,3 linkage. These compounds are useful pharmacophores that offer a broad range of therapeutic applications. Pyrazoles can be synthesized by (i) the condensation of 1,3 dipolar compounds and alkenes/alkynes, (b) cyclocondensation of hydrazines and dicarbonyl reagents, and (c) multi-component reactions. Access to thiazoles is typically via (a) the condensation of α-haloketones with nucleoph
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You might also be interested in the extended bibliographies on the topic '2-c]thiazoles' for particular source types:
Journal articles
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