Relevant bibliographies by topics / Thiazolo

Contents

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

Academic literature on the topic 'Thiazolo'

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

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Journal articles on the topic "Thiazolo"

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Hosseini, Akram Karbalaee, and Azadeh Tadjarodi. "Luminescent MOFs Based on Thiazolo[5,4-d]thiazole as a Chemosensor for the Detection of Environmental Contaminants." Journal of Nanotechnology and Nanomaterials 5, no. 1 (2024): 1–6. http://dx.doi.org/10.33696/nanotechnol.5.047.

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Luminescent metal-organic frameworks (LMOFs) are considered special candidates for the sensation and detection of particular analytes. Thiazolo[5,4-d]thiazoles (TTZs) are an ideal type of heterocycles for fluorophores with π-bridge moieties demonstrating structure-function characteristics. LMOFs with excellent sensing properties can be constructed by incorporating heterocyclic aromatic thiazolo[5,4-d]thiazole into the framework. This study has elaborated on LMOFs containing thiazolo[5,4-d]thiazole unit for the detection of environmental contaminants, such as toxic anions, aromatic compounds, a
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Vinogradov, Dmitry B., Alexei N. Izmest’ev, Angelina N. Kravchenko, Yuri A. Strelenko, and Galina A. Gazieva. "Synthesis of imidazo[4,5-e][1,3]thiazino[2,3-c][1,2,4]triazines via a base-induced rearrangement of functionalized imidazo[4,5-e]thiazolo[2,3-c][1,2,4]triazines." Beilstein Journal of Organic Chemistry 19 (July 28, 2023): 1047–54. http://dx.doi.org/10.3762/bjoc.19.80.

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A series of imidazo[4,5-e][1,3]thiazino[2,3-c][1,2,4]triazines was synthesized via a cascade sequence of hydrolysis and skeletal rearrangement of imidazo[4,5-e]thiazolo[2,3-c][1,2,4]triazin-7(8H)-ylidene)acetic acid esters in methanol upon treatment with excess KOH. Imidazo[4,5-e]thiazolo[3,2-b][1,2,4]triazin-6(7H)-ylidene)acetic acid esters are also suitable substrates for the reaction. In this case hydrolysis and thiazole ring expansion were accompanied with the change of the thiazolotriazine junction type from thiazolo[3,2-b][1,2,4]triazine to thiazino[2,3-c][1,2,4]triazine.
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Borysiuk, Olha, Vasyl Zhylko, Lesya Saliyeva, et al. "Synthesis and biological activity of 2-arylidene-5,6-dihydroimidazo[2,1-b]thiazoles and 6,7-dihydro-5h-[1,3]thiazolo[3,2-a]pyrimidines." ScienceRise: Pharmaceutical Science, no. 2 (54) (April 30, 2025): 22–28. https://doi.org/10.15587/2519-4852.2025.326521.

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The aim. The present study is devoted to searching for potential biologically active agents among functionalized imidazo[2,1-b]thiazoles and thiazolo[3,2-a]pyrimidines. Materials and methods. The interaction of preparatively available 5,6-dihydroimidazo[2,1-b]thiazolone and 6,7-dihydro-2H-thiazolo[3,2-a]pyrimidinone with several substituted benzaldehydes in boiling acetic acid in the presence of anhydrous sodium acetate leads to new 2-arylidene-substituted 5,6-dihydroimidazo[2,1-b]thiazoles and 6,7-dihydro-5H-[1,3]thiazolo[3,2-a]pyrimidines as potential pharmacological agents. Their antimicrob
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Tokárová, Zita, and Anna Biathová. "Synthesis and structure-physicochemical properties relationship of thiophene-substituted bis(5,4-d)thiazoles." Nova Biotechnologica et Chimica 17, no. 2 (2018): 193–200. http://dx.doi.org/10.2478/nbec-2018-0020.

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Abstract Substituted thiophene-2-carbaldehydes 1a-dwere utilized in the synthesis of symmetrically substituted thiazolo[5,4-d]thiazoles 3a-d. Bis(5,4-d)thiazoles with thiophene core at the termini are the most employed in the chemistry of materials but exhibit insufficient solubility in majority of organic solvents with notable impact on the low yields of products. Accordingly, the synthetic approach towards 2,5-dithiophen- 2-yl-thiazolo[5,4-d]thiazole (3a) and its substituted derivatives 3b-d is discussed under the various reaction conditions. Appropriate structural characterisations are incl
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Slyvka, N. Yu, L. M. Saliyeva, V. I. Zhylko, V. M. Tkachuk, and M. V. Vovk. "Synthesis and antioxidant activity of new 2-(2-oxoindoline-3-ylydene) substituted 5,6-dihydroimidazo[2,1-b]thiazolones and 6,7-dihydro-thiazolo[3,2-a]pyrimidinones." Voprosy Khimii i Khimicheskoi Tekhnologii, no. 1 (February 2025): 71–79. https://doi.org/10.32434/0321-4095-2025-158-1-71-79.

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The paper presents the results of the study on the interaction of 5,6-dihydroimidazo[2,1-b]thiazoles and 6,7-dihydrothiazolo[3,2-a]pyrimidines with isatin derivatives. It was established that the condensation of the indicated reagents occurs selectively upon heating and without the use of a catalyst with the formation of addition products, 2-(2-oxoindolin-3-ylidene)-5,6-dihydroimidazo[2,1-b]thiazole-3(2H)-ones 6a–d and 2-(2-oxoindolin-3-ylidene)-6,7-dihydro-2H-thiazolo[3,2-a]pyrimidin-3(5H)-ones 7a–c, the structure of which was rigorously proven by 1H NMR (13C) spectroscopy and chromatography-
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Tokárová, Zita, Renáta Gašparová, Natália Kabaňová, Marcela Gašparová, and Róbert Balogh. "Hemetsberger–Knittel and Ketcham Synthesis of Heteropentalenes with Two (1:1), Three (1:2)/(2:1) and Four (2:2) Heteroatoms." Reactions 4, no. 2 (2023): 254–73. http://dx.doi.org/10.3390/reactions4020015.

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The synthetic methods leading to furo[3,2-b]pyrroles and thiazolo [5,4-d]thiazoles are reviewed herein. Furo-, thieno- and seleno [3,2-b]pyrroles are related to heteropentalenes, containing two heteroatoms in the entire structure, one each per core. The synthetic approach follows the Hemetsberger–Knittel protocol covering three reaction steps—the nucleophilic substitution of halogen-containing aliphatic carboxylic acid esters, Knoevenagel condensation and, finally, thermolysis promoting the intramolecular cyclocondensation to O,N-heteropentalene. The Hemetsberger–Knittel reaction sequence is a
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Nguyễn, Thiên Thuý Trang, Jean-François Longevial, and Stéphanie Hesse. "Synthesis of Thiazolo[5,4-d]thiazoles in an Eco-Friendly L-Proline–Ethylene Glycol Mixture." Molecules 30, no. 4 (2025): 938. https://doi.org/10.3390/molecules30040938.

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The hazardousness of solvents used in synthetic organic chemistry is well established. In this context, it is relevant to search for safer and greener alternatives. Within the last decades, deep eutectic solvents have been considered as possible and promising alternatives. Consequently, this study aims at using deep eutectic solvents to synthesize an emerging class of heteroaromatic compounds named thiazolo[5,4-d]thiazoles, for which interest is growing in the field of organics, electronics, and biology. To address this challenge, we developed a straightforward synthetic protocol consisting of
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Fizer, O. I., M. M. Fizer, A. O. Kryvoviaz, and M. V. Slivka. "INVESTIGATION OF THE INFLUENCE OF THE SUBSTITUTE IN THE THIRD POSITION ON THE ELECTRONIC STRUCTURE OF 1,3-THIAZOLO[2,3-c][1,2,4]TRIAZOLE." Scientific Bulletin of the Uzhhorod University. Series «Chemistry» 46, no. 2 (2022): 55–62. http://dx.doi.org/10.24144/2414-0260.2021.2.55-62.

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Condensed 1,2,4-triazole derivatives exhibit a wide range of biological activity. In particular, triazolam, alprazolam and estazolam, which contain [1,2,4]triazolo[4,3-a][1,4]benzodiazepine system, are used as tranquilizers. Brotizolam is another tranquilizer, a derivative of thieno[3,2-f][1,2,4]triazolo [4,3-a][1,4]diazepine. The oral hypoglycemic drug sitagliptin contains the [1,2,4]triazolo[4,3-a]pyrazine system. In addition, pesticides such as flumetsulam, metosulam, cloransulam, diclosulam, florasulam, are derivatives of [1,2,4]triazolo[1,5-a]pyrimidine, [1,2,4]triazolo[1,5-c]pyrimidine a
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Hua, Shuanghui, Jimin Moon, and Taeho Lee. "The Facile Solid-Phase Synthesis of Thiazolo-Pyrimidinone Derivatives." Molecules 30, no. 2 (2025): 430. https://doi.org/10.3390/molecules30020430.

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A thiazolo-pyrimidinone derivative library was developed through a facile solid-phase synthesis method. For the reaction, the thiazolo[4,5-d]pyrimidin-7(6H)-one structure was synthesized through efficient Thorpe–Ziegler and cyclization reactions. The thiazolo[4,5-d]pyrimidin-7(6H)-one derivative library with a diversity of three had a total of four synthesis steps and 57 compounds. In addition, the yield per synthesis step was 65–97%, which was very high. The developed synthesis method and compounds will be used to find compounds with biological activity through the thiazole derivative structu
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Olgun, U., and M. Gülfen. "Effects of different dopants on the band gap and electrical conductivity of the poly(phenylene-thiazolo[5,4-d]thiazole) copolymer." RSC Adv. 4, no. 48 (2014): 25165–71. http://dx.doi.org/10.1039/c4ra02425g.

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Dissertations / Theses on the topic "Thiazolo"

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Chabert-Morel, Sandrine. "Synthèse, physiochimie et étude biologique de thiazolo, imodazo, dioxolo et cyclopent acridines." Aix-Marseille 3, 1994. http://www.theses.fr/1994AIX30090.

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La condensation de 5-amino et de 6-aminobenzothiazoles substitues, de 5-amino-1,3-dihydro-2h-benzimidazol-2-one, de 5-amino-1,3-benzodioxane et de 5-aminoindane avec de l'acidechlorobenzoique selon la methode de ullman a permis l'obtention d'un acide anthranilique intermediaire. La cyclisation intramoleculaire de ce compose peut conduire a l'obtention de deux isomeres. Selon la nature du quatrieme cycle: thiazole, imidazole, dioxole, dioxane ou cyclopentane on obtient l'isomere lineaire, l'isomere coude ou un melange des deux. Dans ce dernier cas, la mise au point d'une methode de separation c
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Couly, Florence. "Modifications fonctionnelles en position C2 des 8-alkylthiazolo[5,4-f]quinazolin-9(8H)-ones et stratégie d’extension de fragment pour la synthèse d’inhibiteurs de kinases de la famille DYRK." Thesis, Normandie, 2018. http://www.theses.fr/2018NORMIR12/document.

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Les effets du dérèglement de l’expression des protéines kinases DYRK (Dual-specificity tyrosine phosphorylation-regulated kinase) et plus particulièrement de DYRK1A sont étudiées dans le cas des maladies neurodégénératives (maladie d’Alzheimer, syndrome de Down) et celui de certains cancers. Ces travaux de thèse s’inscrivent dans la continuité des acquis du laboratoire et des résultats des évaluations de l’activité inhibitrice obtenus sur les thiazolo[5,4-f]quinazolines et les thiazolo[5,4-f]quinazolin-9(8H)-ones. L’objectif principal est la modulation du groupement en position C2 des thiazolo
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Hanoun, Jean-Pierre. "Synthèse et physico-chimie de pentacycles et de bétai͏̈nes imidazo et thiazolo acridinoniques : étude de l'équilibre azide/tétrazole." Aix-Marseille 3, 1996. http://www.theses.fr/1996AIX30102.

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Les acridines sont des molecules polycycliques planes qui peuvent s'inserer dans la structure helicoidale du dna. Elles sont reconnues comme etant des agents mutagenes. Parmi leurs derives, les acridinones possedent une activite contre de nombreuses formes de cancers. A partir de tetracycles imidazo et thiazolo acridinoniques, l'association du triazole ou du tetrazole permet d'acceder a de nouveaux pentacycles. Dans le cas de la 7-butyltetrazolo1',5':1,5thiazolo5,4-aacridin-12-one, la molecule presente un equilibre azide/tetrazole, lequel varie en fonction de la polarite du solvant. La synthes
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Gillard, Alain-Claude. "Synthèse et étude physico-chimique de pyrrolo [2,1-c] et de thiazolo[4,3-c] [1,4] benzodiazépines à visée thérapeutique." Caen, 1996. http://www.theses.fr/1996CAEN4057.

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Tardieu, Pascale. "Synthèse de spiro[indoline-(pyrimidino, thiazolo ou triazolo)-benzoxazines] : étude de leurs caractéristiques photochromiques en solution et matrice polymérique." Aix-Marseille 2, 1991. http://www.theses.fr/1991AIX22001.

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Trois series originales de spiro indoline-oxazines photochromes (pyrimidino, thiazolo, triazolo-benzoxazines) ayant necessite l'elaboration de differents precurseurs alpha-nitroso beta-hydroxy heteroaromatiques, ont ete preparees. La determination, par photolyse a eclairs des parametres caracterisant le photochromisme a permis de situer ces composes par rapport a leurs homologues spiro indoline-naphtoxazines pris comme reference. Les modifications de structure apportees sur la partie oxazine n'induisent pas de variations sensibles de la stabilite thermique des formes colorees, mais elargissent
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Le, Meur Mikaël. "Identification de nouveaux inhibiteurs de l’agrégation de la protéine Tau." Thesis, Orléans, 2014. http://www.theses.fr/2014ORLE2046.

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Parmi la vingtaine de pathologies neurodégénératives recensées à ce jour, il a été retrouvé des caractéristiques communes telles que des lésions neuronales. Dans le cas de la Maladie d’Alzheimer, une dégénérescence neurofibrillaire a notamment été mise en évidence, ce qui se traduit par l’agrégation de protéines Tau anormalement modifiées. Bien que les mécanismes moléculaires impliqués demeurent encore mal compris, nous nous sommes intéressés, au cours de cette thèse, à la synthèse puis à l’évaluation biologique de nouveaux inhibiteurs de l’agrégation de la protéine TAU impliquée dans la Malad
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Ghewa, El Achkar. "Propriétés anti-inflammatoires des statines, des triterpénoïdes et des dérivés de thiazole : rôle de la hème-oxygénase-1 et de la cyclooxygénase-2." Thesis, Paris Est, 2015. http://www.theses.fr/2015PESC0033.

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Les statines sont des inhibiteurs sélectifs de la 3-hydroxy-3-méthylglutaryl-coenzyme A réductase, utilisées pour diminuer la biosynthèse du cholestérol. Ces molécules possèdent en plus de leur capacité à réduire le cholestérol des effets pléiotropiques comme les propriétés anti-inflammatoires et anti-oxydantes. Les cucurbitacines sont des triterpènes dérivés des plantes, ayant des propriétés biologiques diverses comme les effets anti-inflammatoires et anticancéreux, associées toutefois à une toxicité élevée. Les dérivés de thiazole sont des molécules contenant un noyau hétérocyclique formé de
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Jouve, Karine. "Préparations et cycloadditions [4+2] in situ d'o-quinodiméthanes du thiazole : étude de la régiosélectivité des réactions de Diels-Alder vis-à-vis des diénophiles dissymétriques de type acétylénique, éthylénique et quinonique." Lyon 1, 1999. http://www.theses.fr/1999LYO1T097.

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Ostache, Nicu-Carmin. "Synthèse et fonctionnalisation de bicycles 5-5 polyazotés : pyrazolo[3,4-d]thiazoles et pyrazolo[3,4-c]pyrazoles." Thesis, Orléans, 2019. http://intranet.univ-orleans.fr/bibliotheques/theses/nicu-cosmin-ostache_3378_vm.pdf/.

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Les structures bicycliques azotées sont parmi les entités les plus utilisées dans le domaine thérapeutique.Les bicycles 5:5 polyazotés sont des structures moins décrites que leurs analogues 6:6 ou6:5. Malgré le potentiel pharmacologique des pyrazolo [3,4-d] thiazoles et des pyrazolo [3,4-c] pyrazoles,deux exemples de ces familles rares, seuls quelques procédés de préparation et de fonctionnalisationdirecte de ces charpentes hétérocycliques sont décrits.De ce fait, l’objectif principal de nos recherches vise à développer de nouvelles voies de synthèse vers cesdeux charpentes bicycliques et ce,
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Grubb, Alan M. "Preparation of Heteroatom-Substituted 1,3-Thiazoles as Building Blocks for Liquid Crystal Synthesis." Kent State University / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=kent1322507000.

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Books on the topic "Thiazolo"

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Sowoidnich, Werner. Neue Chelate der Benzthiazol- und Benzobisthiazolreihe: Darstellung und spektroskopische Eigenschaften. Hartung-Gorre, 1989.

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Jenny, Christian-Johannes. Synthese und Reaktionen von 2-Thiazolin-5-thionen. [s.n.], 1986.

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Babu, B. Synthesis of Condensed Thiazolo-[3,2-a] Pyrimidine Systems. Routledge, 1991.

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Maass, Gerhard. Charakterisierung der Thiazolo-iso-indolinone, einer neuen Klasse nichtnukleosidischer Inhibitoren der Reversen Transkriptase von HIV-1. 1993.

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Svadlenka, Anton. Thiazole: Synthesis and Reactions. Nova Science Publishers, Incorporated, 2020.

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Thiazole: Synthesis and Reactions. Nova Science Publishers, Incorporated, 2020.

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Metzger, Jacques V. Thiazole and Its Derivatives, Part 3. Wiley & Sons, Incorporated, John, 2008.

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Metzger, Jacques V. Thiazole and Its Derivatives, Part 1. Wiley & Sons, Incorporated, John, 2009.

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Metzger, Jacques V. Thiazole and Its Derivatives, Part 1. Wiley & Sons, Incorporated, John, 2008.

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Metzger, Jacques V. Thiazole and Its Derivatives, Part 2. Wiley & Sons, Incorporated, John, 2009.

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Book chapters on the topic "Thiazolo"

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Hegde, Shridhar G., Martin D. Mahoney, and Claude R. Jones. "Thiazolo[4,5-b]pyridine-3(2H)-acetic Acid Derivatives." In ACS Symposium Series. American Chemical Society, 1995. http://dx.doi.org/10.1021/bk-1995-0584.ch007.

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Dwivedi, Shreya, Ram Kishore, and Nitin Srivastava. "Novel Synthesis of 3,5-Disubstituted-5H-Thiazolo[3,2-α]Pyrimidine." In Global Trends in Health, Technology and Management. Springer Nature Switzerland, 2024. https://doi.org/10.1007/978-3-031-75457-9_20.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of trinuclear nickel(II) complex with thiazolo-2,4-pentanedione." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_447.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of trinuclear copper(II) complex with thiazolo-2,4-pentanedione." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_569.

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Kaur, Navjeet. "Thiazole Synthesis." In Lawesson’s Reagent in Heterocycle Synthesis. Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-4655-3_2.

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Rauf, Abdul, and Nida Nayyar Farshori. "Thiazoles." In SpringerBriefs in Molecular Science. Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-1485-4_3.

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Demaison, J. "272 C3H3NS Thiazole." In Asymmetric Top Molecules. Part 2. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-10400-8_20.

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Begtrup, Mikael, and Christian Roussel. "Mesoionic Thiazoles." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187074.ch1.

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Li, Jie Jack. "Cook-Heilbron thiazole synthesis." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_66.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear copper(II) acetate complex with ligand derived from the condensation of thiazolo-2, 4-pentanedione with 1, 6-diaminohexane." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_264.

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Conference papers on the topic "Thiazolo"

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Shuchi, Nuren, Tyler Adams, V. Paige Stinson, et al. "Complex Dielectric Function of Photochromic Thiazolothiazole Embedded Polymers Determined by Spectroscopic Ellipsometry." In CLEO: Applications and Technology. Optica Publishing Group, 2024. http://dx.doi.org/10.1364/cleo_at.2024.jth2a.10.

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The complex dielectric function of photochromic thiazolo[5,4-d]thiazole embedded in polymer is reported in the spectral range from 0.8 to 2.5 eV. Strong absorption bands in the measured spectral range are observed depending upon its redox states.
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Váry, Tomáš, Zita Tokárová, and Vojtech Nádaždy. "Energy resolved electrochemical impedance spectroscopy of furan-substitued thiazolo [5,4-d]thiazoles." In APPLIED PHYSICS OF CONDENSED MATTER (APCOM 2021). AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0067189.

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Zhang, Weiyi, Gang Zhou, and Zhong-Sheng Wang. "Thiazolo[5,4-d]thiazole-Based Organic Dyes for Quasi-Solid-State Dye-Sensitized Solar Cells." In Advanced Optoelectronics for Energy and Environment. OSA, 2013. http://dx.doi.org/10.1364/aoee.2013.asa3a.12.

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Gabitova, Elina, Artem Agarkov, Mariya Mailyan, et al. "Synthesis of Triazolyl Derivatives Based on Thiazolo[3,2-a]pyrimidine Propargyl Ethers." In ECSOC 2024. MDPI, 2024. https://doi.org/10.3390/ecsoc-28-20126.

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Besson, Thierry, Damien Hédou, Corinne Fruit, et al. "Synthesis and biological evaluation of new thiazolo [5,4-f]quinazolines as serine/threonine kinases inhibitors." In 1st International Electronic Conference on Medicinal Chemistry. MDPI, 2015. http://dx.doi.org/10.3390/ecmc-1-a047.

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Ali, Noor H., A. H. Saleh, Muayad Al-Dulaimi, Eman Abd Al-Salam, and Mohammed Hasan Mohammed. "A new route to thiazolo quinazoline derivatives and novel synthesis of pyrido, pyrimidoquinazoline as potential anticancer agents." In 2ND INTERNATIONAL CONFERENCE ON MATHEMATICAL TECHNIQUES AND APPLICATIONS: ICMTA2021. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0103406.

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Jabar, Maha A., and Nisreen H. Karam. "Designed new mesogence containing 5H-thiazolo[3,4-b][1,3,4]ihiadiazole: Synthesis and investigation of liquid crystals properties." In THE SECOND INTERNATIONAL SCIENTIFIC CONFERENCE (SISC2021): College of Science, Al-Nahrain University. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0120896.

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Prasad, N. L., M. S. Krishnamurthy, and Noor Shahina Begum. "Crystal structure studies of methyl 3-amino-2-cyano-5-(2-fluoro-phenyl)-7-methyl-5H-thiazolo [3,2-a]pyrimidine-6-carboxylate." In WORLD MULTIDISCIPLINARY CIVIL ENGINEERING-ARCHITECTURE-URBAN PLANNING SYMPOSIUM WMCAUS 2022. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0174743.

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Besson, Thierry, Florence Couly, Carole Dubouilh-benard, Laurent Meijer, and Corinne Fruit. "Late-stage C-H Arylation of Thiazolo[5,4-f]quinazolin-9(8H)-one Backbone: Synthesis of an Array of Potential Kinase Inhibitors." In 3rd International Electronic Conference on Medicinal Chemistry. MDPI, 2017. http://dx.doi.org/10.3390/ecmc-3-04650.

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Besson, Thierry, Damien Hédou, Carole Dubouilh-benard, Nadège Loaëc, Laurent Meijer, and Corinne Fruit. "Synthesis of Bioactive 2-(arylamino)thiazolo[5,4-f]-quinazolin-9-ones via the Hügershoff Reaction or Cu- Catalyzed Intramolecular C-S Bond Formation." In 2nd International Electronic Conference on Medicinal Chemistry. MDPI, 2016. http://dx.doi.org/10.3390/ecmc-2-a010.

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