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Relevant bibliographies by topics / Oxazolo

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Academic literature on the topic 'Oxazolo'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Oxazolo"

1

Tsygankova, V.A., Ya.V. Andrusevich, O.I. Shtompel, S.G. Pilyo, A.M. Kornienko, and V.S. Brovarets. "Using of [1,3]oxazolo[5,4-d]pyrimidine and N-sulfonyl substituted of 1,3-oxazole to improve the growth of soybean seedlings." Chemistry Research Journal 3, no. 2 (2018): 165–73. https://doi.org/10.5281/zenodo.13923631.

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The effect of the chemical low molecular weight heterocyclic compounds, derivatives of [1,3]oxazolo[5,4-<em>d</em>]pyrimidine and N-sulfonylsubstituted of 1,3-oxazole on stimulation of root and shoot growth of soybean seedlings (<em>Glycine max </em>L.) cultivar Valuta was studied. The growth regulating activity of the heterocyclic compounds derivatives of [1,3]oxazolo[5,4-<em>d</em>]pyrimidine and N-sulfonyl substituted of 1,3-oxazole was compared with the growth regulating activity of the plant hormone auxin NAA (1-Naphthylacetic acid). It was found that the chemical heterocyclic compounds u

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2

Blancou, Wafa, Badr Jismy, Soufiane Touil, Hassan Allouchi, and Mohamed Abarbri. "Simple and Expedient Access to Novel Fluorinated Thiazolo- and Oxazolo[3,2-a]pyrimidin-7-one Derivatives and Their Functionalization via Palladium-Catalyzed Reactions." Molecules 27, no. 9 (2022): 3013. http://dx.doi.org/10.3390/molecules27093013.

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An efficient, versatile, and one-pot method for the preparation of novel fluorinated thiazolo- and oxazolo[3,2-a]pyrimidin-7-ones is described from 2-aminothiazoles or 2-amino-oxazoles and fluorinated alkynoates. This transformation, performed under transition-metal-free conditions, offers new fluorinated cyclized products with good to excellent yields. Moreover, the functionalization of these N-fused scaffolds via the Suzuki-Miyaura and Sonogashira cross-coupling reactions led to the synthesis of highly diverse thiazolo- and oxazolo[3,2-a]pyrimidin-7-ones.

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3

Velihina, Y. S., S. G. Pilyo, I. V. Ivanova, and V. S. Brovarets. "Synthesis of pyrazolo[1,5-a][1,3,5]triazine and oxazolo[4,5-d]pyrimidine derivatives and study of their vasodilator activity." Voprosy Khimii i Khimicheskoi Tekhnologii, no. 2 (May 2023): 51–60. http://dx.doi.org/10.32434/0321-4095-2023-147-2-51-60.

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A number of pyrazolo[1,5-a][1,3,5]triazine and oxazolo[4,5-d]pyrimidine derivatives were synthesized and characterized. Pyrazolo[1,5-a][1,3,5]triazines with various substituents in the fourth position and a dichloromethyl group in the second position were obtained by the heterocyclization reaction of available N-(2,2-dichloro-1-cyanoethenyl)carboxamides and 5-aminopyrazoles. Oxazolo[4,5-d]pyrimidines were obtained by treating 2-phenyl-4-dichloromethylene-1,3-oxazol-5(4H)-one with the corresponding arylamidine hydrochloride in the presence of triethylamine. The resulting 4,5-dihydro-1H-imidazol

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4

Olczak, Andrzej, Jarosław Sukiennik, Beata Olszewska, Monika Stefaniak, Krzysztof Walczyński, and Małgorzata Szczesio. "Structures 4-n-propyl Piperazines as Non-Imidazole Histamine H3 Antagonists." Materials 14, no. 22 (2021): 7094. http://dx.doi.org/10.3390/ma14227094.

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Seven new low-temperature structures of 4-n-propylpiperazine derivatives, potential H3 receptor antagonists, have been determined by X-ray crystallography, with the following symmetry and unit cell parameters: 2-(4-propyl-piperazin-1-yl)oxazolo[4,5-c]pyridine (compound 1), P-1, 5.9496 Å, 12.4570 Å, 12.8656 Å, 112.445°, 95.687°, 103.040°; 2-(4-propyl-piperazin-1-yl)thia-zolo[4,5-c]pyridine (compound 2), I2/a, 22.2087 Å, 7.5519 Å, 19.9225 Å, β = 92.368°; 2-(4-propyl-piperazin-1-yl)oxazolo[5,4-c]pyridine (compound 3), C2/c, 51.1351 Å, 9.36026 Å, 7.19352 Å, β = 93.882°; 2-(4-propyl-piperazin-1-yl)

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5

Golikov, A. G., P. V. Reshetov, O. I. Korneeva, and M. O. Netreba. "STEREOSTRUCTURE OF SUBSTITUTED OXAZOLO(OXAZINO)HYDROQUINOLINES." Chemistry and Technology of Organic Substances, no. 2 (2018): 4–14. http://dx.doi.org/10.54468/25876724_2018_2_4.

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6

Bremner, JB, CL Raston, GL Rowbottom, AH White, and KN Winzenberg. "A Ring Destruction Approach to Some Benzo-Fused Medium-Sized Heterocycles by Means of Cyanogen-Bromide Under Solvolytic Conditions - X-Ray Structure of a '1h-2,6-Benzoxazecine-6-Carbonitrile and a '2h-3,6-Benzoxazecine-6-Carbonitrile Derivative." Australian Journal of Chemistry 39, no. 6 (1986): 893. http://dx.doi.org/10.1071/ch9860893.

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Reaction of the reduced pyrrolo [2,1-a] isoquinoline amine (1a) with cyanogen bromide in the presence of methanol gave the medium-ring cyanamide derivative 7,9,10-trimethoxy-2,3,4,5,6,7-hexahydro-1H-3- benzazonine-3-carbonitrile (2a). Analogous products were also obtained from reaction of the reduced 5H-oxazolo[2,3-a] isoquinoline , 2H- benzo [a] quinolizine , 2H,6H-[1,3] oxazino [2,3-a] isoquinoline and [1,4] oxazino [3,4-a] isoquinoline derivatives (1b-e), whereas the reduced 3H-oxazolo[4,3-a] isoquinoline and 5H-oxazolo[2,3-a] isoquinoline derivatives (1f) and (8) gave 1-(2,4-dioxapentyl)-6

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7

Akula, Mahesh, Yadagiri Thigulla, Connor Davis, Mukund Jha, and Anupam Bhattacharya. "Synthesis of 4-substituted oxazolo[4,5-c]quinolines by direct reaction at the C-4 position of oxazoles." Organic & Biomolecular Chemistry 13, no. 9 (2015): 2600–2605. http://dx.doi.org/10.1039/c4ob02224f.

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Cu(TFA)<sub>2</sub> catalysed synthesis of 4-arylsubstituted oxazolo[4,5-c]quinolines/[1,8] naphthyridines has been described via a modified Pictet–Spengler method, without prefunctionalization of the unreactive 4<sup>th</sup> position of oxazoles.

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8

Aly, Ashraf A., Alaa A. Hassan, Nasr K. Mohamed, et al. "Synthesis of New Fused Heterocyclic 2-Quinolones and 3-Alkanonyl-4-Hydroxy-2-Quinolones." Molecules 24, no. 20 (2019): 3782. http://dx.doi.org/10.3390/molecules24203782.

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Herein, we report the synthesis of 5,12-dihydropyrazino[2,3-c:5,6-c′]difuro[2,3-c:4,5-c′]-diquinoline-6,14(5H,12H)diones, 2-(4-hydroxy-2-oxo-1,2-dihydroquinolin-3-yl)-1,4-diphenyl- butane-1,4-diones and 4-(benzo-[d]oxazol-2-yl)-3-hydroxy-1H-[4,5]oxazolo[3,2-a]pyridine-1-one. The new candidates were synthesized and identified by different spectroscopic techniques, and X-ray crystallography.

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9

Ilavský, Dušan, Katarína Heleyová, Jana Nádaská, and Vladimír Bobošík. "Gould-Jacobs Reaction of 5- and 6-Amino-2-substituted Benzoxazoles. I. Reaction with Diethyl Ethoxymethylenemalonate." Collection of Czechoslovak Chemical Communications 61, no. 2 (1996): 268–75. http://dx.doi.org/10.1135/cccc19960268.

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Reaction of 2-substituted 5- and 6-aminobenzoxazoles 1 and 2 with diethyl ethoxymethylenemalonate afforded the corresponding diethyl 3-N-(5- and 6-benzoxazolyl)aminomethylenemalonates 3 and 4. Under conditions of the Gould-Jacobs reaction, the compounds 3 gave a mixture of angularly and linearly annelated oxazolo[4,5-f]quinolones 5 and oxazolo[5,4-g]quinolones 6, and compounds 4 afforded a mixture of oxazolo[5,4-f]quinolones 7 and oxazolo[4,5-g]quinolones 8.

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10

Tsygankova, V.A., Ya.V. Andrusevich, O.I. Shtompel, A.M. Kornienko, V.S. Brovarets, and S.G. Pilyo. "Acceleration of vegetative growth of wheat (Triticum aestivum L.) using [1,3]oxazolo[5,4-d]pyrimidine and N-sulfonyl substituted 1,3-oxazole." Pharmaceutical and Chemical Journal 5, no. 2 (2018): 167–75. https://doi.org/10.5281/zenodo.13904610.

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Wheat (<em>Triticum aestivum</em> L.) is an important cereal crop cultivated in the most economically developed coutries. The elaboration of new effective growth regulators for intensification of seed germination stage and vegetative growth of wheat is an actual problem for modern agriculture. In our work the comparative analysis of regulating activity of low molecular weight heterocyclic compounds, derivatives of [1,3]oxazolo[5,4-<em>d</em>]pyrimidine and N-sulfonyl substituted of 1,3-oxazole, and plant hormones auxins IAA (1<em>H</em>-Indol-3-ylacetic acid) and NAA (1-Naphthylacetic acid) on

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Dissertations / Theses on the topic "Oxazolo"

1

Riederer, Cordula. "Zur Synthese von Tetrahydro-oxazolo[4,3-c]-1,2,4-oxadiazol-5-onen und Tetrahydro-oxazolo[4,3-c]-1,2,4-oxadiazin-6-onen aus 4-Hydroxyimino-oxazolidin-2-onen." [S.l. : s.n.], 1999. http://www.sub.uni-hamburg.de/disse/68/riederer.PDF.

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2

Trethewey, A. N. "Synthesis and evaluation of perhydro-oxazolo [3,4-a] pyridines as fungicides." Thesis, University of Portsmouth, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.354382.

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3

Fernandes, Liana da Silva. "Síntese de 2-amino(alcoxi)-5-trifluoracetil-1,2,3,4-tetraidropiridinas e oxazolo[3,2-a]piridinas." Universidade Federal de Santa Maria, 2006. http://repositorio.ufsm.br/handle/1/10382.

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior<br>The present work describes the synthesis of novel 2-alkoxy-5-trifluoroacetyl-1,2,3,4-tetrahydropyridines, 2-amino-5-trifluoroacetyl-1,2,3,4-tetrahydropyridines and oxazolo[3,2-a]pyridines from the cyclocondensation reactions between 2-alkoxy-5-trifluoroacetyl-2H-3,4-dihydropyranes and aminomethyl pyridines, aminoalcohols and o-aminophenol, respectively, in good yields (72-96%). The 2-alkoxy-5-trifluoroacetyl-1,2,3,4-tetrahydropyridines were synthesized using stoichiometric amounts of the trifluoroacetyl dihydropyranes and three dif

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4

Jones, Garry B. "Design, synthesis and evaluation of DNA-binding oxazolo[2,3-c][1,4]benzodiazepines and pyrrolo[2,1-c][1,4]benzodiazepines." Thesis, University of Portsmouth, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.293269.

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5

Brière, Jean-François. "Elaboration d'une enzyme artificielle se liant à des fonctions amines et des fonctions acides dans le but de catalyser la formation de liaisons amides." Rouen, 1998. http://www.theses.fr/1998ROUES097.

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Ce travail décrit l'élaboration d'un catalyseur supramoléculaire de structure hétérocyclique devant accélérer la formation de liaisons amides, en mimant les mécanismes enzymatiques. Une première synthèse à partir de la 4-amino-3-bromoisoquinoléine a ouvert deux nouvelles voies d'accès aux 2-méthyloxazolo[5,4-c]isoquinoléine et 1H-pyrrolo[3,2-c]isoquinoléine. Cette dernière structure a été fonctionnalisée en position 2 à l'aide d'une réaction de métallation. Au cours de la deuxième voie de synthèse nous avons établi l'influence de la substitution de la fonction amine d'aminopyrrolidine-2,5-dion

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6

Radspieler, Alexander. "Untersuchungen zur Synthese von Diazonamid A und Phorbazol A und C." Doctoral thesis, [S.l. : s.n.], 2000. http://deposit.ddb.de/cgi-bin/dokserv?idn=960868712.

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7

Wong, Yung-Sing. "Nouveaux intermediaires chiraux de type 1,4-dihydropyridine et equivalents de sels de 3,4-dihydropyridinium pour la synthese asymetrique de piperidines polysubstituees. Application a la synthese enantioselective du 3-ppp et de l'indolizidine 195b." Paris 11, 1994. http://www.theses.fr/1994PA112105.

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L'application de la reaction de zincke a des amines primaires enantiomeriquement pures a donne des sels de pyridinium portant un centre asymetrique directement fixe sur l'azote, a partir de la pyridine correspondante, substituee ou non en position 3. L'etude de la reduction par le dithionite de sodium de ces sels a conduit de maniere efficace a de nouveaux intermediaires 1,4-dihydropyridines chiraux. La reduction des sels n-substitues par une chaine phenylethanol donne des 1,4-dihydropyridines qui s'isomerisent en 3,7,8,8a-tetrahydro-2h-oxazolo3,2-apyridines. Une etude structurale a ete entrep

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8

Santos, Taianne D'Angelo dos. "Estudo da aplicação de derivados oxazolônicos como sondas fluorescentes e solvatocrômicas na investigação de solventes puros." Universidade Estadual do Oeste do Paraná, 2018. http://tede.unioeste.br/handle/tede/4156.

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Submitted by Marilene Donadel (marilene.donadel@unioeste.br) on 2019-03-22T20:26:53Z No. of bitstreams: 1 Taianne_Santos_2018.pdf: 3173420 bytes, checksum: 18942f680866870efd7ed25716d1d429 (MD5)<br>Made available in DSpace on 2019-03-22T20:26:53Z (GMT). No. of bitstreams: 1 Taianne_Santos_2018.pdf: 3173420 bytes, checksum: 18942f680866870efd7ed25716d1d429 (MD5) Previous issue date: 2018-12-13<br>This work reports the use of two oxazolonic derivatives, 4- (4- (N, N) dimethylaminobenzylidene) -2-phenyl-1,3-oxazol-5 (4H) -one (AZA2) and 4- (4- nitrobenzylidene) -2-phenyl-1,3-oxazol-5 (4H) -one

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9

Lüdtke, Karin. "Fluoreszenzmarkierte Poly(2-oxazolin)e." [S.l.] : [s.n.], 2005. http://deposit.ddb.de/cgi-bin/dokserv?idn=978987861.

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Flegeau, Emmanuel Ferrer. "Palladium cross-couplings of oxazoles." Thesis, University of Edinburgh, 2008. http://hdl.handle.net/1842/3171.

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A review covering the literature until April 2008 concerning organometallic reactions to funcionalise oxazoles is described. A protocol for the functionalisation of the oxazole 2- and 4-positions using the Suzuki coupling reaction is described. 2- Aryl-4-trifloyloxazoles undergo rapid, microwave-assisted coupling with a range of aryl and heteroaryl boronic acids in good to excellent yields. The methodology is similarly effective using 4-aryl-2-chlorooxazoles as the coupling partner and has been extended to the synthesis of a novel class of homo- and heterodimeric 4,4- linked dioxazoles. In add

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Books on the topic "Oxazolo"

1

Trethewey, Andrew Nicholas. Synthesis and evaluation of perhydro-oxazolo [3,4-a] pyridines as fungicides. Portsmouth Polytechnic, 1985.

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2

Jones, Gary B. Design, synthesis and evaluation of DNA-binding oxazolo[2,3-c][1,4] benzodiazepines and pyrrolo[2,1-c][1,4] benzodiazepines. Portsmouth Polytechnic, School of Pharmacy and Biomedical Sciences, 1991.

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3

J, Turchi I., ed. Oxazoles. Wiley, 1986.

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Palmer, David C., ed. Oxazoles: Synthesis, Reactions, and Spectroscopy. John Wiley & Sons, Inc., 2004. http://dx.doi.org/10.1002/0471649295.

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5

C, Palmer David, ed. Oxazoles: Synthesis, reactions, and spectroscopy. Wiley, 2003.

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6

Schwarzenbach, Elmar. Kationische ringöffnende Polymerisation von bicyclischen Acetalen und von 2-Phenyl-2-Oxazolin [Phenyl-Oxazolin]. [s.n.], 1987.

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Palmer, David C., ed. Oxazoles: Synthesis, Reactions, and Spectroscopy, Part A. John Wiley & Sons, Inc., 2003. http://dx.doi.org/10.1002/0471428035.

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8

Lapkin, I. I. Slozhnye ėfiry [alʹfa]-okso- i [alʹfa]-oksikislot. UrO AN SSSR, 1990.

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9

Grünanger, Paolo. Isoxazoles. Wiley, 1991.

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Turchi, I. J. Oxazoles. Wiley & Sons, Incorporated, John, 2009.

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Book chapters on the topic "Oxazolo"

1

Brovarets, V. S., O. P. Mityukhin, A. V. Golovchenko, and B. S. Drach. "Syntheses of Fluorinated 1,3-Oxazoles, 1,3,4-Oxadiazoles, 1,3,4-Thiadiazoles, and Oxazolo[4,5-d]pyrimidines." In ACS Symposium Series. American Chemical Society, 2009. http://dx.doi.org/10.1021/bk-2009-1003.ch013.

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2

Rauf, Abdul, and Nida Nayyar Farshori. "Oxazoles." In SpringerBriefs in Molecular Science. Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-94-007-1485-4_2.

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3

Beyer, Karl-Heinz. "Oxazolam." In Biotransformation der Arzneimittel. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-74386-3_237.

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Mizuno, Tooru M., Ashwini Padhi, Naomi Fineberg, et al. "Oxazolam." In Encyclopedia of Psychopharmacology. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_1742.

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5

Turchi, Ignatius J. "Oxazoles." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187289.ch1.

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Li, Jie Jack. "Fischer oxazole synthesis." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_107.

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Li, Jie Jack. "Fischer oxazole synthesis." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_99.

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Demaison, J. "269 C3H3NO Oxazole." In Asymmetric Top Molecules. Part 2. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-10400-8_17.

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Knight, David W. "Oxazole and Its Derivatives." In Heterocycles in Natural Product Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527634880.ch12.

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Li, Jie Jack. "van Leusen oxazole synthesis." In Name Reactions. Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03979-4_278.

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Conference papers on the topic "Oxazolo"

1

Guillon, Jean, François Hallé, Solène Savrimoutou, Stéphane Moreau, Daniel-Henri Caignard, and Pascal Sonnet. "Synthesis and Evaluation of New 6-formyl-oxazolo[3,2-a]pyrimidine derivatives as Potential Src Kinase Inhibitors." In 4th International Electronic Conference on Medicinal Chemistry. MDPI, 2018. http://dx.doi.org/10.3390/ecmc-4-05566.

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Kobayashi, Kaori, and Shozo Tsunekawa. "MICROWAVE SPECTROSCOPY OF OXAZOLE AND ISOXAZOLE." In 74th International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2019. http://dx.doi.org/10.15278/isms.2019.ti07.

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LaVoie, Edmond J., Young Ah Kim, Mavurapu Satyanarayana, et al. "Abstract C76: Oxazole‐containing macrocyles as selective G‐quadruplex stabilizers." In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Nov 15-19, 2009; Boston, MA. American Association for Cancer Research, 2009. http://dx.doi.org/10.1158/1535-7163.targ-09-c76.

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Adkins, Taylor, Robert McMahon, R. Woods, et al. "OXAZOLE: PRECISE SEMI-EXPERIMENTAL EQUILIBRIUM STRUCTURE DETERMINATION BY ROTATIONAL SPECTROSCOPY." In 2021 International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2021. http://dx.doi.org/10.15278/isms.2021.fk04.

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Esselman, Brian, and Robert McMahon. "SEMI-EXPERIMENTAL EQUILIBRIUM STRUCTURE OF 1,3-OXAZOLE FROM MANY ISOTOPOLOGUES." In 2023 International Symposium on Molecular Spectroscopy. University of Illinois at Urbana-Champaign, 2023. http://dx.doi.org/10.15278/isms.2023.6893.

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Choudhary, Dimple, and Harvinder Singh Sohal. "A report on synthesis and applications of small heterocyclic compounds: Oxazole." In INTERNATIONAL CONFERENCE ON HUMANS AND TECHNOLOGY: A HOLISTIC AND SYMBIOTIC APPROACH TO SUSTAINABLE DEVELOPMENT: ICHT 2022. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0128710.

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Putri, Chantika Octaviani, and Antonius Herry Cahyana. "Synthesis and antioxidant activity screening of thiazole and oxazole derivative compounds." In INTERNATIONAL CONFERENCE ON SCIENCE AND APPLIED SCIENCE (ICSAS) 2021. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0072502.

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Kuznetsova, Rimma T., Tat'yana N. Kopylova, K. M. Degtjarenko, et al. "Effect of excitation conditions on photostability of 2-(4pyridyl)-5 phenyl)oxazole laser media." In Second Conference on Pulsed Lasers: Pulsed Atomic and Molecular Transitions, edited by Victor F. Tarasenko, Georgy V. Mayer, and Gueorgii G. Petrash. SPIE, 1995. http://dx.doi.org/10.1117/12.216900.

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Douhal, A., F. Lahmani, A. Zehnacker-Rentien та F. Amat-Guerri. "Ultrafast excited-state H-atom transfer in jet-cooled 2-(2ʹ-hydroxyphenyl)-oxazole derivatives". У The 54th international meeting of physical chemistry: Fast elementary processes in chemical and biological systems. AIP, 1996. http://dx.doi.org/10.1063/1.50150.

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Oberhauser, B., B. Grohmann, and H. Sperner. "Selective Epimerisation of a Fungal Cyclopeptolide via an 2-Amino-oxazole Intermediate - Conformational Consequences." In The 2nd International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1998. http://dx.doi.org/10.3390/ecsoc-2-01702.

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