Academic literature on the topic 'Benzo[1,3]oxazoles'

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Journal articles on the topic "Benzo[1,3]oxazoles"

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Ivakhnenko, Eugeny P., Nadezhda I. Makarova, Mikhail I. Knyazhansky, et al. "Photochemical Generation, Photochromism and Photocyclization of 2-Norbornadenyl Substituted Benzo-1,3-Oxazoles." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 297, no. 1 (1997): 233–37. http://dx.doi.org/10.1080/10587259708036127.

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Yan, Shaoxi, Leping Ye, Miaochang Liu, et al. "Unexpected TFA-catalyzed tandem reaction of benzo[d]oxazoles with 2-oxo-2-arylacetic acids: synthesis of 3-aryl-2H-benzo[b][1,4]oxazin-2-ones and cephalandole A." RSC Adv. 4, no. 32 (2014): 16705–9. http://dx.doi.org/10.1039/c4ra01605j.

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Hou, Xiu-Feng, Quan Zhou, Shu Liu, et al. "N-Heterocyclic Carbene (NHC)-Catalyzed One-Pot Aerobic Oxidative Synthesis of 2-Substituted Benzo[d]oxazoles, Benzo[d]thiazoles and 1,2-Disubstituted Benzo[d]imidazoles." Synthesis 50, no. 06 (2017): 1315–22. http://dx.doi.org/10.1055/s-0036-1591524.

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N-Heterocyclic carbene (NHC), generated in situ from easily available N-heterocyclic imidazolium salt with air as terminal oxidant, has successfully been utilized as a cheap and efficient catalyst for one-pot aerobic oxidative synthesis of 2-arylbenzo[d]oxazoles, 2-substituted benzo[d]thiazoles, and 1,2-disubstituted benzo[d]imidazoles.
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García-Ramírez, Verónica G., Claudia Contreras-Celedón, Gabriela Rodriguez-García, Luis Chacón-García, and Carlos J. Cortes-García. "Synthesis of 1,3-Oxazoles via Van Leusen Reaction in a Pressure Reactor and Preliminary Studies of Cations Recognition." Proceedings 41, no. 1 (2019): 7. http://dx.doi.org/10.3390/ecsoc-23-06463.

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Six 1,3-oxazoles were synthetized in moderate to good yields by Van Leusen reaction in a pressure reactor. The methodology allowed to decrease the reaction times reported in the literature from hours to 20 min. In addition, preliminary qualitative recognition of cations with some synthetized oxazoles such as Hg2+, Ni2+, Zn2+, Ag+, Cu2+, Pb2+ was done and a “turn off” effect was observed with Ni2+. Finally, the 1,3-oxazoles could be of biological relevance because they are considered privileged nucleus in medicinal chemistry and therefore will be useful to obtain pharmacophoric hybrid molecules
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Yang, Liangru, Jinwei Yuan, Pu Mao, and Qi Guo. "Chelating palladium complexes containing pyridine/pyrimidine hydroxyalkyl di-functionalized N-heterocyclic carbenes: synthesis, structure, and catalytic activity towards C–H activation." RSC Advances 5, no. 130 (2015): 107601–7. http://dx.doi.org/10.1039/c5ra21183b.

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Rajanarendar, Eligeti, Paka Venkateshwarlu, Saini Ramakrishna, and Dharavath Nagaraju. "A Mild and Efficient Synthesis of Novel Isoxazolyl-Benzo[d]Pyrazino[2,1-b] [1,3]Oxazoles." Journal of Heterocyclic Chemistry 52, no. 4 (2014): 1007–13. http://dx.doi.org/10.1002/jhet.2064.

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Hashmi, A. Stephen K. "Gold-catalyzed synthesis of N,O-heterocycles." Pure and Applied Chemistry 82, no. 3 (2010): 657–68. http://dx.doi.org/10.1351/pac-con-09-10-17.

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The selective synthesis of oxazoles, alkylidene oxazoles, and 1,3-oxazines from N-propargyl carboxamides by choosing gold(III) or gold(I) catalysts and selecting terminal or internal alkynes as substrates is discussed. The mechanistic studies based on labeling experiments and intensive in situ NMR studies indicate an anti-oxyauration step and a proto-deauration with retention of the sterical arrangement at the double bond. The synthetic scope for gold(I) catalysts is very broad, allowing selective conversions to products with properties of chelate ligands, reactions of bromoarenes and the form
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Freeman, Fillmore, Tao Chen, and Johannes B. van der Linden. "Synthesis of Highly Functionalized 1,3-Oxazoles." Synthesis 1997, no. 08 (1997): 861–62. http://dx.doi.org/10.1055/s-1997-1296.

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Shirinian, Valerii, Ilya Lonshakov, Alexey Zakharov, Andrey Lvov, and Mikhail Krayushkin. "Practical Deoxygenation of Oxazole N-Oxides by PCl3/Collidine." Synthesis 51, no. 02 (2018): 414–20. http://dx.doi.org/10.1055/s-0037-1610278.

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A new chemoselective method for the synthesis of 2-aryl-1,3-oxazoles by deoxygenation of the corresponding N-oxides has been developed. As the deoxygenation reagent, a previously unknown complex of collidine with phosphorus trichloride in a 2:1 ratio has been used. The developed method enabled the preparation of a wide range of 2-aryl-1,3-oxazoles comprising various functional groups in good yields. The advantage of this reagent is its tolerance to nitro, methyl, hydroxyl, formyl, and acetyl groups, and double bonds. Due to chemoselectivity and availability of reagents, the method may be used
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Rajanarendar, Eligeti, Paka Venkateshwarlu, Saini Ramakrishna, and Dharavath Nagaraju. "ChemInform Abstract: A Mild and Efficient Synthesis of Novel Isoxazolyl-benzo[d]pyrazino[2,1-b][1,3]oxazoles." ChemInform 46, no. 48 (2015): no. http://dx.doi.org/10.1002/chin.201548172.

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Dissertations / Theses on the topic "Benzo[1,3]oxazoles"

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Ella, Ndong Guy Judicaël. "Synthèses régiosélectives d'hétérocycles porteurs d'un groupement perfluoroalkyle." Thesis, Tours, 2015. http://www.theses.fr/2015TOUR4036/document.

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Dans ce travail, de nombreux hétérocycles porteurs d’un groupement CF3 ou C2F5 ont été décrits : des cétals, des benzo[1,3]dixoles, des pyran-2H-ones, des isocoumarines, des benzofuranes et des indolo[2,3-c]pyran-1-ones. Ces hétérocycles représentent une classe importante de produits biologiquement actifs. L’hydroalkoxylation intermoléculaire des dérivés du 4,4,4-perfluorobut-2-ynoate d’éthyle en présence d’une quantité catalytique de sodium métallique dans des conditions simples et douces a permis la synthèse de cétals fluorés d’une manière totalement régiosélective. La méthodologie a été éte
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Baekelmans, Didier. "Synthèse de benzo-indolizines par cycloaddition 1,3 dipolaire." Doctoral thesis, Universite Libre de Bruxelles, 1998. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/212087.

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Hron, Rebecca. "Design, Synthesis and Glioblastoma Activity of 1,3-Diazinane Based Aryl Amides and Benzo Fused Heterocycles." ScholarWorks@UNO, 2017. http://scholarworks.uno.edu/td/2301.

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The development of novel targeted therapeutics for the treatment of cancer remains difficult due to the complex nature of the disease itself as well as the challenges associated with the synthesis of these therapeutics. Impediments to the discovery of novel drug candidates include lack of available starting materials and access to well-developed syntheses which are both convenient and economically feasible. Semicarbazides, for instance, are a critical synthon for the manufacture of numerous biologically important molecules. Historically, convenient methods for the synthesis of semicarbazides a
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Wang, Xuefeng. "Fonctionalisation de naphtalèn-1,4 dione : Synthèse et applications dans les dispositifs biocapteurs." Paris 7, 2014. http://www.theses.fr/2014PA077052.

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Les biocapteurs électrochimiques ont connu un grand bond en avant ces dernières décennies compte tenu de leurs nombreuses utilisations potentielles. Dans ce travail, deux biocapteurs électrochimiques originaux, ne nécessitant ni réactif, ni marquage, sont développés pour la détection directe d'une part d'un biomarqueur protéique et d'autre part d'un polluant organique. Pour le premier, la sonde peptidique est couplée avec un dérivé de juglone pour former le H-AVPFAQK(JugAcid)G¬NH2 (JAP). Il est ensuite co-polymérisé avec la juglone sur une électrode de carbone poreux. L'électrode modifiée prés
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SAKELLARIOU, FARGUES REINE. "Reactivite chimique et photochimique d'alpha -enones dans les milieux organises." Toulouse 3, 1986. http://www.theses.fr/1986TOU30044.

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Dans une premiere partie on determine les zones monophasiques des diagrammes des phases pseudoternaires de plusieurs microemulsions. Dans l'une d'elles l'isophorone remplace l'huile. Ensuite les chapitres ii et iii sont consacres aux reactions de photocycloaddition (a+a, a+b) d'alpha -enones (isophorone, coumarine, dimethylthymine). On montre que les phenomenes observes sont lies aux differentes localisations possibles des substrats, aux mecanismes de reaction et aux structures des milieux. En conclusion, la localisation des reactifs a l'interface permet la combinaison des effets de concentrat
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李惠玲. "Synthesis of 2-Amino-Benzo[e][1,3]thiazin-4-ones Derivatives and Studies of Their Central Nervous System Activities." Thesis, 2002. http://ndltd.ncl.edu.tw/handle/35405530903726413041.

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碩士<br>台北醫學院<br>藥學研究所<br>90<br>Abstract A facile synthesis of 2-amino-benzo[e][1,3]thiazin-4-one derivatives was achieved. A methanolic solution of 2-methylsulfanyl-benzo[e][1,3] thizin-4-one was treated with various amine compounds at 25℃. The amine compounds are ammonia water, n-butylamine, n-octylamine, hydroxylamine, 3-aminopropanol, ethylenediamine, N,N-dimethylethyl- enediamine, aminoacetaldehyde dimethylacetal, triethylamine, piperidine, piperazine, N-ethylpiperazine, morpholine, (S)-(+)-2-methanol- pyrrolidine, aniline, and p-phenetidine. The reaction completed i
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Hsiao, Ming-Yu, та 蕭明玉. "Synthesis of 1,3-Benzoxazines via π-insertion reactions of Arynes and N-Acyl imines and Chemoselective Intramolecular Wittig Reactions for the Synthesis of Oxazoles and Benzofurans". Thesis, 2015. http://ndltd.ncl.edu.tw/handle/ubfus5.

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Yawer, Mirza Arfan [Verfasser]. "Synthesis of functionalized 6-(pyridyl)salicylates, bis(benzophenones), chlorinated 6H-benzo[c]chromen-6-ones based on new cyclocondensations of 1,3-bis(silyloxy)-1,3-butadienes / vorgelegt von Mirza Arfan Yawer." 2008. http://d-nb.info/991250540/34.

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Tolaymat, Ibrahim [Verfasser]. "1,4-benzothiazepines, 3-hydroxy-benzo[b]thiophene-2-carboxamides and benzothieno[2,3-e][1,3]oxazines derived from thiosalicylic acid / by Ibrahim Tolaymat." 2009. http://d-nb.info/994097840/34.

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Books on the topic "Benzo[1,3]oxazoles"

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High Nitrogen Explosives. Part 2. Dibenzo-1 ,3a,4,6a- Tetraazapentalenes and Benzo-1 2,3,4-Tetrazine-1,3-Dioxides. Storming Media, 1996.

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Book chapters on the topic "Benzo[1,3]oxazoles"

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Joule, J. A., K. Mills, and G. F. Smith. "1,3-Azoles: imidazoles, thiazoles and oxazoles: reactions and synthesis." In Heterocyclic Chemistry. Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-3222-8_21.

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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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Saritha, K., and G. Rajitha. "Molecular Properties Prediction of N-((benzo[1,3]dioxol-5-yl)methylene)-2-cyano-3-Substituted Phenylacrylohydrazides." In Learning and Analytics in Intelligent Systems. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-46939-9_57.

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Schukat, G., and E. Fanghänel. "1,3-(Benzo)Thiatellurolium and 1,3-(Benzo)Selenatellurolium Salts." In Five-Membered Hetarenes with One Chalcogen and One Additional Heteroatom. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-011-00360.

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Gudat, D. "1,3-(Benzo)Thiaphospholes." In Five-Membered Hetarenes with One Chalcogen and One Additional Heteroatom. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-011-01151.

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Schukat, G., and E. Fanghänel. "1,3-(Benzo)Dithiolium Salts." In Five-Membered Hetarenes with One Chalcogen and One Additional Heteroatom. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-011-00304.

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Schukat, G., and E. Fanghänel. "1,3-(Benzo)Thiaselenolium Salts." In Five-Membered Hetarenes with One Chalcogen and One Additional Heteroatom. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-011-00337.

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Schukat, G., and E. Fanghänel. "1,3-(Benzo)Diselenolium Salts." In Five-Membered Hetarenes with One Chalcogen and One Additional Heteroatom. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-011-00347.

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Schukat, G., and E. Fanghänel. "1,3-(Benzo)Ditellurolium Salts." In Five-Membered Hetarenes with One Chalcogen and One Additional Heteroatom. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-011-00357.

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Wipf, Peter. "1,3-Oxazoles and -Thiazoles in Natural Product Synthesis." In 19th International Congress on Heterocyclic Chemistry. Elsevier, 2003. http://dx.doi.org/10.1016/b978-0-08-044304-1.50029-0.

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Conference papers on the topic "Benzo[1,3]oxazoles"

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Li-Zhulanov, Nikolai, Alla Pavlova, Dina Korchagina, et al. "Synthesis of novel benzo[1,3]oxazines based on monoterpenoid (–)-isopulegol and study of their analgesic activity." In 6th International Electronic Conference on Medicinal Chemistry. MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07380.

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