Relevant bibliographies by topics / Isoxazoles

Contents

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

Academic literature on the topic 'Isoxazoles'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Isoxazoles"

1

Fuse, Shinichiro, Taiki Morita, and Hiroyuki Nakamura. "Step-by-Step Multifunctionalization of Isoxazoles Based On SEAr Reactions and C–H Direct Arylations." Synthesis 49, no. 11 (April 18, 2017): 2351–60. http://dx.doi.org/10.1055/s-0036-1588784.

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Functionalized isoxazoles are important as pharmaceuticals and agrochemicals. Generally, electrophilic aromatic substitution or generation of carbanions/electrophilic trapping approach is used to introduce functional groups into unsubstituted heteroaromatics. However, these approaches have not been simple to apply to unsubstituted isoxazoles due to their poor nucleophilicity and instability under basic conditions. Recently several approaches have been reported to overcome these problems. This review summarizes the functionalization of isoxazoles, including SEAr reactions and C–H direct arylations, towards the step-by-step multifunctionalization of isoxazoles.1 Introduction2 SEAr Reaction of Isoxazoles3 Preparation of Isoxazolyl Anions and Their Use for the Synthesis of Functionalized Isoxazoles4 Other C–C and C–N Bond Formations of Isoxazoles5 Transition-Metal-Catalyzed C–H Direct Functionalization of Isoxazoles6 Step-by-Step Multifunctionalization of Isoxazoles7 Summary and Outlook
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Yoshimura, Akira, Akio Saito, Viktor V. Zhdankin, and Mekhman S. Yusubov. "Synthesis of Oxazoline and Oxazole Derivatives by Hypervalent-Iodine-Mediated Oxidative Cycloaddition Reactions." Synthesis 52, no. 16 (May 18, 2020): 2299–310. http://dx.doi.org/10.1055/s-0040-1707122.

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Organohypervalent iodine reagents are widely used for the preparation of various oxazolines, oxazoles, isoxazolines, and isoxazoles. In the formation of these heterocyclic compounds, hypervalent iodine species can serve as the activating reagents for various substrates, as well as the heteroatom donor reagents. In recent research, both chemical and electrochemical approaches toward generation of hypervalent iodine species have been utilized. The in situ generated active species can react with appropriate substrates to give the corresponding heterocyclic products. In this short review, we summarize the hypervalent-iodine­-mediated preparation of oxazolines, oxazoles, isoxazolines, and isoxazoles starting from various substrates.1 Introduction2 Synthesis of Oxazolines3 Synthesis of Oxazoles4 Synthesis of Isoxazolines5 Synthesis of Isoxazoles6 Conclusion
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Fershtat, Leonid L., Daniil A. Chaplygin, Ivan V. Ananyev, and Nina N. Makhova. "Divergent Synthesis of Five-Membered Nitrogen Heterocycles via Cascade Reactions of 4-Arylfuroxans." Synthesis 52, no. 18 (May 5, 2020): 2667–78. http://dx.doi.org/10.1055/s-0040-1707393.

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A novel method for the synthesis of a diverse series of functionally substituted five-membered heterocyclic compounds via atom-economic, regio-, and diastereoselective one-pot reaction cascade was developed. This approach involves a ring opening in 4-arylfuroxans to α-oximinoarylacetonitrile oxides followed by [3+2] cycloaddition to various dipolarophiles to afford multisubstituted isoxazoles and isoxazolines. Subsequent azole–azole rearrangement of (oximino)isoxazolines/-isoxazoles, which can be conducted in a one-pot manner, results into functionally substituted furazans formation. The developed protocol is operationally simple, proceeds in mild conditions and with high yields of target heterocyclic systems. Overall, this study represents a new mode of isoxazole and 1,2,5-oxadiazole functionalization strategy, which is useful in medicinal and materials chemistry.
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Chikkula, Krishna Veni, and Raja S. "ISOXAZOLE – A POTENT PHARMACOPHORE." International Journal of Pharmacy and Pharmaceutical Sciences 9, no. 7 (July 1, 2017): 13. http://dx.doi.org/10.22159/ijpps.2017.v9i7.19097.

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Isoxazole is an azole with an oxygen atom next to the nitrogen. Isoxazole rings are found in some natural products, such as ibotenic acid and also found in a number of drugs, including COX-2 inhibitor valdecoxib. Furoxan, a nitric oxide donor is containing isoxazolyl group & found in many β-lactamase resistant antibiotics, such as cloxacillin, dicloxacillin and flucloxacillin. The synthetic androgenic steroid danazol also has an isoxazole ring. The substituted isoxazoles are well developed in literature to posses significant biological activities. The disubstituted and trisubstituted isoxazoles have been reported to exhibit broad range of biological activities such as antimicrobial activity, analgesic activity, antiinflammatory activity, antioxidant activity, anticancer activity, CNS activity, antitubercular activity and miscellaneous activities like GABA agonistic activity, inhibitory activity, antihypertensive activity, and glutamate transporter activity. The present review summarizes up to date information of various biological activities of isoxazole analogs.
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Griesbeck, Axel G., Marco Franke, Jörg Neudörfl, and Hidehiro Kotaka. "Photocycloaddition of aromatic and aliphatic aldehydes to isoxazoles: Cycloaddition reactivity and stability studies." Beilstein Journal of Organic Chemistry 7 (January 26, 2011): 127–34. http://dx.doi.org/10.3762/bjoc.7.18.

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The first photocycloadditions of aromatic and aliphatic aldehydes to methylated isoxazoles are reported. The reactions lead solely to the exo-adducts with high regio- and diastereoselectivities. Ring methylation of the isoxazole substrates is crucial for high conversions and product stability. The 6-arylated bicyclic oxetanes 9a–9c were characterized by X-ray structure analyses and showed the highest thermal stabilities. All oxetanes formed from isoxazoles were highly acid-sensitive and also thermally unstable. Cleavage to the original substrates is dominant and the isoxazole derived oxetanes show type T photochromism.
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Thirunarayanan, G., and V. Sathiyendiran. "Synthesis, Pharmacological and Insect Antifeedant Activities of some 3-(2-Naphthyl)-5-(Substituted Phenyl)-4,5-Dihydroisoxazoles." International Letters of Chemistry, Physics and Astronomy 49 (April 2015): 1–14. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.49.1.

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Totally thirty one 3,5-substituted aryl 4,5-dihydro isoxazole derivatives including 3-(2-naphthyl)-5-(substituted phenyl)-4,5-dihydroisoxazole have been synthesized by fly-ash:H2SO4 catalyzed cyclization of hydroxylamine hydrochloride and aryl chalcones under solvent-free conditions. The yields of the isoxazoles are more than 94%. The synthesized isoxazole were characterized by their physical constants and spectral data. The antimicrobial, antioxidant and insect antifeedant activities of the synthesized isoxazoles have been evaluated using a variety of bacterial and fungal species, DPPH radical scavenging and castor-leaf disc bioassay of 4th instar larvae Achoea Janata L methods.
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Camoutsis, Ch, and S. Nikolaropoulos. "Steroidal isoxazoles, isoxazolines and isoxazolidines." Journal of Heterocyclic Chemistry 35, no. 4 (July 1998): 731–59. http://dx.doi.org/10.1002/jhet.5570350401.

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Cherton, Jean-Claude, Marc Lanson, Daïf Ladjama, Yvette Guichon, and Jean-Jacques Basselier. "Synthèse d'isoxazoles substitués en α de l'azote par une chaine alkyle ou alcényle." Canadian Journal of Chemistry 68, no. 8 (August 1, 1990): 1271–76. http://dx.doi.org/10.1139/v90-196.

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Several syntheses of special isoxazoles bearing a long alkyl or alkenyl side chain in the α position of the nitrogen are presented. A very convenient route in the case of an alkyl side chain is the classical 1,3-dipolar cycloaddition of a nitrile-oxide to a vinyl acetate. Although it is a rather long approach, the reaction of hydroxylamine with enone-epoxides represents a new and unequivocal method compatible with alkenyl side chains. The isomerisation of the easily synthesized isoxazoles bearing such substitutents α to the oxygen, by the reaction of their isoxazolium salts with hydroxylamine, is a fast and general method. Another very convenient access to "α-N substituted" isoxazoles is the coupling of magnesium compounds with 3-bromomethyl 5-methyl isoxazole. Keywords: isoxazoles, substitution in the α position of nitrogen.
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Svejstrup, Thomas D., Wojciech Zawodny, James J. Douglas, Damon Bidgeli, Nadeem S. Sheikh, and Daniele Leonori. "Visible-light-mediated generation of nitrile oxides for the photoredox synthesis of isoxazolines and isoxazoles." Chemical Communications 52, no. 83 (2016): 12302–5. http://dx.doi.org/10.1039/c6cc06029c.

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Rey, Marine, and Stéphane Beaumont. "Molybdenum-Mediated One-Pot Synthesis of Pyrazoles from Isoxazoles." Synthesis 51, no. 20 (August 26, 2019): 3796–804. http://dx.doi.org/10.1055/s-0039-1690615.

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A one-pot approach for the direct synthesis of substituted pyrazoles from isoxazoles is reported. The process involves isoxazole N–O bond cleavage mediated by a molybdenum complex, in situ hydrolysis of the resulting β-amino enone to the corresponding 1,3-diketone, followed by pyrazole formation in the presence of hydrazine or substituted hydrazine. Good to excellent yields and regioselectivities are obtained with nonsymmetric isoxazoles. By using readily available starting materials, a wide range of substituted pyrazoles may be synthesized by this method.
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Dissertations / Theses on the topic "Isoxazoles"

1

Knight, Julian Gary. "Diphenylphosphinoylalkyk isoxazoles and isoxazolines." Thesis, University of Cambridge, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.306451.

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Tout, Jaki. "The synthesis and reactions of alkenyl isoxazoles and isoxazolines." Thesis, University of Edinburgh, 1993. http://hdl.handle.net/1842/14563.

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Four vinyl-isoxazoles and -2-isoxazolines have been synthesised as potential monomers for polymerisation studies. 5-Phenyl-3-vinylisoxazole was prepared in 38% overall yield by a sequence involving cycloaddition of ethoxycarbonyl-formonitrile oxide to phenylacetylene and then reduction of the resulting 3-carbethoxyisoxazole to the aldehyde using di-isobutylaluminium hydride. In the final stage Wittig olefination of the formyl-isoxazole afforded the target compound. 5-Phenyl-3-vinylisoxazole (17%) and 5-phenyl-3-vinyl-2-isoxazoline (26%) were synthesised similarily from ethyl propiolate & benzohydroximoyl chloride, and styrene & ethyl chlorooximidoacetate, respectively. 3-Phenyl-5-vinyl-2-isoxazoline (84%) was obtained in one step by cycloaddition of benzonitrile oxide to butadiene. An alternative and more direct approach to 3-vinylisoxazolines has been developed based on the cycloaddition reactions of acrylonitrile oxide (ANO), and α,β-unsaturated nitrile oxide. ANO was generated, under modified Mukaiyama conditions, by the dehydration of 1-nitropropene with phenyl isocyanate in the presence of catalytic quantities of triethylamine. ANO was trapped by a variety of olefinic dipolarophiles as its 1,3-dipolar cycloadducts in yields ranging from 17% to 71%. Under similar conditions phenylacetylene reacted in low yield (12%). The series of α,β-unsaturated nitrile oxides was extended to include methacrylonitrile oxide and but-2-enonitrile oxide. The dipolarophilic reactivity series was determined by competition experiments. Six dipolarophiles were investigated: Styrene, α-methylstyrene, methyl acrylate, methyl vinyl ketone and three substituted styrences (p-OMe, p-CI and m-NO2). 13C and 1H NMR spectroscopy were used to identify the products and determine the adduct ratio. The results indicated methyl acrylate to be the most reactive dipolarophile. The 1,1-disubstitution in α-methylstyrene effectively lowered its reactivity due to steric effects.
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Lanson, Marc. "Isoxazoles polyalkyles synthèse, étude structurale et comportement en milieu biologique /." Grenoble 2 : ANRT, 1987. http://catalogue.bnf.fr/ark:/12148/cb376069814.

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Lanson, Marc. "Isoxazoles polyalkyles : synthese, etude structurale et comportement en milieu biologique." Paris 6, 1987. http://www.theses.fr/1987PA066468.

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Duffy, Kevin James. "Studies on the synthesis and reactivity of fused 3,4-isoxazoles." Thesis, University of Edinburgh, 1993. http://hdl.handle.net/1842/13734.

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This thesis is concerned with the synthesis of various fused, 3,4-isoxazoles by the thermal cyclisation of 2-nitroaryl and 2-nitroheteroaryl acetic acid derivatives and the exploitation of the uses of these compounds in heterocyclic synthesis by their reduction to afford 2-aminoaryl and heteroaryl ketones followed by the annulation of these latter derivatives. Heating solutions of 2-(3-nitropyrid-2-yl)propanedioate esters under reflux in inert solvents afforded isoxazolo[4,3-b]pyridine-3-carboxylate derivatives. The successful application of this novel synthesis on a large scale was crucially dependent on the physical removal of the corresponding alcohol component from the reaction mixture. The thermal cyclisation of various 2-substituted 2-(3-nitropyrid-2-yl)ethanoates was also examined and in the case of cyano derivatives afforded the anticipated isoxazolo[4,3-b]pyridines but was less successful for substrates containing keto groups. 2-(3-Nitropyrid-2-yl)ethanoate failed to cyclise to afford the parent isoxazolo[4,3-b]pyridine. Evidence is presented for the involvement of ketene intermediates in these thermal cyclisation reactions. Reduction of the isoxazol[4,3-b]pyridine-3-carboxylate derivatives gave either 2-(3-aminopyrid-2-yl)-2-hydroxyethanoate or 2-(3-aminopyrid-2-yl)-2-oxoethanoate derivatives depending on the substrate, the former compounds being converted into the latter by oxidation with manganese dioxide. Annulation of the 2-(3-aminopyrid-2-yl)-2-oxoethanoates produced then gave a variety of substituted 1,5-napthyridin-2(1H)-one derivatives. The chemical transformations of these new 1,5-napthyridine derivatives was also briefly examined. 1,7-Napthyridin-2(1H)-one derivatives were also prepared by a similar sequence of reactions commencing with the thermal cyclisation of diethyl 2-(3-nitropyrid-4-yl)propanedioate to give ethyl isoxazolo[3,4-c]pyridine-3-carboxylate followed by reductive ring opening of the latter and subsequent annulation of ethyl 2-(3-aminopyrid-4-yl)-2-oxoethanoate so produced.
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Duller, Kathryn April Marion. "A cycloaddition route to heterocyclic tricarbonyl natural products." Thesis, University of Nottingham, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.307821.

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Khatimi, Nadia. "Synthèse d'hétérocycles substitués par un groupe trifluorométhyle (isoxazoles, aziridines, thiophènes, pyrroles)." Lyon 1, 1996. http://www.theses.fr/1996LYO10177.

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Le memoire presente en vue de l'obtention du diplome de doctorat est consacre a la synthese d'heterocycles possedant un groupe trifluoromethyle. La premiere partie presente une synthese originale de plusieurs trifluoromethylisoxazoles. Ces composes ont ete utilises pour preparer des aziridines substituees par une chaine trifluoroethyle. La synthese proposee est stereoselective. Dans le deuxieme chapitre, une synthese totalement stereoselective d'aziridines substituees par un groupe trifluoromethyle est proposee: les aziridines sont obtenues par addition du trifluoromethylsilane sur des azirines. Le dernier chapitre est essentiellement consacre a la synthese et la reactivite d'enamino enones substituees par un groupe trifluoromethyle. Leur cyclisation en pyrrole a ete effectuee et l'etude de differents facteurs, gouvernant une cyclisation 3 exotrig ou 5 exotrig, a ete realisee. A ce jour, ce travail a donne lieu a deux publications parues dans des revues internationales: 1 c. Felix, n. Khatimi et a. Laurent, j. Org. Chem. , 1995, 60, 3907-12. 2 c. Felix, n. Khatimi et a. Laurent, tetrahedron lett. , 1994, 35, 3303-3304
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FALCOU, SERGE, and André Pierre Joseph Rassat. "Utilisation des isoxazoles en synthese : approche de la synthese de la phyllanthocine." Paris 6, 1995. http://www.theses.fr/1995PA066314.

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La synthese de la phyllanthocine et en particulier du systeme spirocetal bicyclique 6,5 fait intervenir la condensation aldolique de l'enolate du 3-acetylisoxazole sur un hydroxyaldehyde methyle. Apres la mise au point de la synthese de cet isoxazole inconnu, et suite a la mauvaise reactivite de l'enolate de cet isoxazole, une modification de la strategie de synthese nous a conduit a realiser un umpolung en condensant un alcynure sur le 3-carbomethoxyisoxazole. Cette strategie permet d'acceder au produit d'aldolisation precedemment souhaite par addition conjuguee diastereoselective d'un hemiacetalate sur une enone convenable dans des conditions basiques. La fermeture du cycle a six centres du spirocetal de la phyllanthocine etant realisee, la coupure reductrice de l'isoxazole a permis d'obtenir le precurseur direct du spirocetal
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Michaud, Thierry. "Synthese d'heterocycles azotes enatiomeriquement purs (aziridines, azetidines, isoxazoles) au depart de monosaccharides." Clermont-Ferrand 2, 1995. http://www.theses.fr/1995CLF21711.

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Un axe important de la chimie des glucides est leur utilisation comme source de chiralite dans la synthese de molecules a proprietes biologiques potentielles. Notre objectif a ete la synthese d'azetidines polyhydroxylees substituees en 2 et 3, enantiomeriquement pures, au depart de monosaccharides. Des ditosylates en 4,6 ont ete prepares en quatre etapes au depart des d-gluco- et d-mannopyranose par acetalisation, c-alkylation, hydrolyse et tosylation. Dans la serie du d-glucopyranose l'action d'amines primaires (methyl-, benzyl-, et tertbutylamine) sur les derives ditosyles permet d'acceder, par l'intermediaire d'un derive monoamine en 6 et monotosyle en 4, a des azetidines fusionnees en 4,6 a un galactopyranoside. Huit azetidines fusionnees ont ete ainsi preparees. Le deblocage des fonctions alcoolprotegees sous forme d'ethers benzyliques, et l'ouverture du cycle pyranose par l'hydrogene en presence d'hydroxyde de palladium sur charbon active conduit a des azetidines polyhydroxylees optiquement pures possedant quatre centres asymetriques. Dans la serie du d-mannopyranose, l'action de la terbutylamine conduit au seul derive 4,6-didesoxy-4,6diaminod-talopyranoside. Les reactions de cycloaddition dipolaire 1,3 des methyl-et benzonitriloxydes sur la 3-bromolevoglucosenone sont regioselectives et conduisent a des isoxazoles fusionnes et substitues en 5 par le groupe carbonyle
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Blackburn, Jack. "The synthesis, attempted synthesis and applications of 1,2,4-oxadiazoles and isothiazolo-isoxazoles." Thesis, University of Huddersfield, 2014. http://eprints.hud.ac.uk/id/eprint/26888/.

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Books on the topic "Isoxazoles"

1

Grünanger, Paolo. Isoxazoles. New York: Wiley, 1991.

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Toong, Samuel Y. Modulation of [alpha]-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA) receptors by a novel organic nitrate ester. Ottawa: National Library of Canada, 1999.

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Grünanger, Paola, and Paola Vita-Finzi. Volume 49, Part 1, Isoxazoles. Wiley-Interscience, 1991.

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Bartlett, Robert R. Leflunomide: Proceedings of the Vienna Symposium, 12 October 1993. Birkhauser, 1995.

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(Editor), Paola Grünanger, Paola Vita-Finzi (Editor), and James E. Dowling (Editor), eds. The Chemistry of Heterocyclic Compounds, Isoxazoles (Chemistry of Heterocyclic Compounds: A Series Of Monographs). Wiley-Interscience, 1999.

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Bartlett, Robert R. Leflunomide: Proceedings of the Vienna Symposium, 12 October 1993. Birkhauser, 1996.

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1947-, Bartlett R. R., ed. Leflunomide: Proceedings of the Vienna symposium, 12 October 1993. Basel: Birkhäuser Verlag, 1995.

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Roy, Amelie. Synthetic studies of the formation of oxazoles and isoxazoles from N-acetoacetyl derivatives: Scope and limitations AND Aqueous rhodium-catalyzed Heck-type coupling reactions between boronic acids and olefins. 2000.

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Book chapters on the topic "Isoxazoles"

1

Quilico, Adolfo. "Isoxazoles." In Chemistry of Heterocyclic Compounds: A Series Of Monographs, 5–94. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186787.ch1.

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Quilico, Adolfo. "Isoxazoles and Related Compounds." In Chemistry of Heterocyclic Compounds: A Series Of Monographs, 1–4. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186787.part1.

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Gandolfig, Remo, and Paolo Grünanger. "Partially Saturated Polynuclear Isoxazoles." In Chemistry of Heterocyclic Compounds: A Series Of Monographs, 467–870. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470187364.ch4.

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Badenock, Jeanese C. "Metalation Reactions of Isoxazoles and Benzisoxazoles." In Topics in Heterocyclic Chemistry, 261–305. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/7081_2012_80.

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Joule, J. A., K. Mills, and G. F. Smith. "1,2-Azoles: pyrazoles, isothiazoles and isoxazoles: reactions and synthesis." In Heterocyclic Chemistry, 394–408. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-3222-8_22.

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Silva, Artur M. S., Augusto C. Tomé, Teresa M. V. D. Pinho e Melo, and José Elguero. "Five-Membered Heterocycles: 1,2-Azoles. Part 2. Isoxazoles and Isothiazoles." In Modern Heterocyclic Chemistry, 727–808. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527637737.ch9.

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Ballistreri, Francesco Paolo, Ugo Chiacchio, Antonio Rescifina, Gaetano Andrea Tomaselli, and Rosa Maria Toscano. "Formation of Isoxazolines and Isoxazoles Via Dipolar Cycloaddition by Catalytic Oxidation of Aldoximes with Hydrogen Peroxide and W(Vi) Peroxo Complexes." In The Activation of Dioxygen and Homogeneous Catalytic Oxidation, 446. Boston, MA: Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-3000-8_37.

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Quilico, Adolfo. "Isoxazolines." In Chemistry of Heterocyclic Compounds: A Series Of Monographs, 95–115. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186787.ch2.

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Demaison, J. "270 C3H3NO Isoxazole." In Asymmetric Top Molecules. Part 2, 49–50. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-10400-8_18.

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Li, Jie Jack. "Claisen isoxazole synthesis." In Name Reactions, 115–16. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_55.

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Conference papers on the topic "Isoxazoles"

1

Amaral, Simone Schneider, and Paulo Henrique Schneider. "Regioselective Synthesis of 3-Haloalkyl-isoxazoles from the Electrophilic Cyclization of Halogenated Oximes." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0053-1.

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

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Silva-Alves, Diana C. B. da, Janaína V. dos Anjos, Nery N. M. Cavalcante, Daniela M. do A. F. Navarro, Geanne K. N. Santos, and Rajendra M. Srivastava. "Synthesis of new isoxazole derivatives with larvicidal activity." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0284-1.

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Vilela, G. D., R. R. da Rosa, and A. A. Merlo. "Isoxazole Derivatives With Potential Applications in Polymers and Semiconductors." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0032-1.

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Nurjanah, N., and E. Saepudin. "Curcumin isolation, synthesis and characterization of curcumin isoxazole derivative compound." In PROCEEDINGS OF THE 4TH INTERNATIONAL SYMPOSIUM ON CURRENT PROGRESS IN MATHEMATICS AND SCIENCES (ISCPMS2018). AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5132492.

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Liu, Hongliang, Gang Liu, and Weijun Liu. "Photochromism and optical recording of a novel diarylethene bearing isoxazole unit." In 2011 4th International Congress on Image and Signal Processing (CISP 2011). IEEE, 2011. http://dx.doi.org/10.1109/cisp.2011.6100550.

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Yamini, G., G. Sravya, Grigory V. Zyryanov, and A. Padmaja. "Ultrasound promoted synthesis of pyrazolyl/isoxazolyl oxadiazoles as antimicrobials." In PROCEEDINGS OF INTERNATIONAL CONFERENCE ON RECENT TRENDS IN MECHANICAL AND MATERIALS ENGINEERING: ICRTMME 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0018634.

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Li, Xiaoting, Weijun Liu, Shouzhi Pu, and Hui Li. "Synthesis and Properties of Photochromic Diarylethene Derivatives Bearing Benzofuran and Isoxazole Units." In 2012 Symposium on Photonics and Optoelectronics (SOPO 2012). IEEE, 2012. http://dx.doi.org/10.1109/sopo.2012.6271041.

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Li, Hui, Shouzhi Pu, Gang Liu, and Shiqiang Cui. "Synthesis and Property upon a New Photochromic Diarylethene Bearing an Isoxazole Moiety." In 2011 Symposium on Photonics and Optoelectronics (SOPO 2011). IEEE, 2011. http://dx.doi.org/10.1109/sopo.2011.5780587.

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Kearns, Alison K., Mariusz P. Gajewski, Nicholas R. Natale, and Howard D. Beall. "Abstract 1767: Anthracenyl isoxazole amides (AIMs) as novel agents for brain tumors." In Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-1767.

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