Collection of Czechoslovak Chemical Communications - digital archive 

Crossref Cited-by Linking

• Melekhova Anna A., Smirnov Andrey S., Novikov Alexander S., Panikorovskii Taras L., Bokach Nadezhda A., Kukushkin Vadim Yu.: Copper(I)-Catalyzed 1,3-Dipolar Cycloaddition of Ketonitrones to Dialkylcyanamides: A Step toward Sustainable Generation of 2,3-Dihydro-1,2,4-oxadiazoles. ACS Omega 2017, 2, 1380. <https://doi.org/10.1021/acsomega.7b00130>
• Maiuolo Loredana, De Nino Antonio, Merino Pedro, Russo Beatrice, Stabile Gaetano, Nardi Monica, D’Agostino Napoleone, Bernardi Tatiana: Rapid, efficient and solvent free microwave mediated synthesis of aldo- and ketonitrones. Arabian Journal of Chemistry 2016, 9, 25. <https://doi.org/10.1016/j.arabjc.2015.01.015>
• Anisimova Tatyana B., Kinzhalov Mikhail A., Kuznetsov Maxim L., Guedes da Silva M. Fátima C., Zolotarev Andrey A., Kukushkin Vadim Yu., Pombeiro Armando J. L., Luzyanin Konstantin V.: 1,3-Dipolar Cycloaddition of Nitrones to Gold(III)-Bound Isocyanides. Organometallics 2016, 35, 3569. <https://doi.org/10.1021/acs.organomet.6b00635>
• Michael Ryan E., Chando Katelyn M., Sammakia Tarek: Synthesis of N-Vinyl Nitrones via 1,4-Conjugate Elimination. J. Org. Chem. 2015, 80, 6930. <https://doi.org/10.1021/acs.joc.5b01138>
• Smirnov Andrey S., Yandanova Ekaterina S., Bokach Nadezhda A., Starova Galina L., Gurzhiy Vladislav V., Avdontceva Margarita S., Zolotarev Andrey A., Kukushkin Vadim Yu.: Zinc(ii)-mediated generation of 5-amino substituted 2,3-dihydro-1,2,4-oxadiazoles and their further ZnII-catalyzed and O2-involving transformations. New J. Chem. 2015, 39, 9330. <https://doi.org/10.1039/C5NJ02061A>
• Mehrdad Morteza, Faraji Laleh, Jadidi Khosrow, Eslami Parisa, Sureni Hossein: A regioselective and diastereoselective synthesis of new spiro-isoxazolidines via 1,3-dipolar cycloaddition of stable isatin ketonitrone and various dipolarophiles. Monatsh Chem 2011, 142, 917. <https://doi.org/10.1007/s00706-011-0518-2>
• Beckett A H, Coutts R T, Ogunbona F A: The structure of nitrones derived from amphetamines. Journal of Pharmacy and Pharmacology 2011, 26, 312. <https://doi.org/10.1111/j.2042-7158.1974.tb09281.x>
• Beckett A H, Gibson G G: Identification of the in vitro N-oxidized metabolites of (+)- and (−)-N-benzylamphetamine. Journal of Pharmacy and Pharmacology 2011, 29, 756. <https://doi.org/10.1111/j.2042-7158.1977.tb11456.x>
• Pfeiffer Jennifer Y., Beauchemin André M.: Simple Reaction Conditions for the Formation of Ketonitrones from Ketones and Hydroxylamines. J. Org. Chem. 2009, 74, 8381. <https://doi.org/10.1021/jo901653d>
• Moran Joseph, Pfeiffer Jennifer Y., Gorelsky Serge I., Beauchemin André M.: Ketonitrones via Cope-Type Hydroamination of Allenes. Org. Lett. 2009, 11, 1895. <https://doi.org/10.1021/ol900292r>
• Murphy John A., Mahesh Mohan, McPheators Gary, Anand R. Vijaya, McGuire Thomas M., Carling Robert, Kennedy Alan R.: Fragmentation of Nitrone Triflates to 9-Membered Rings. Org. Lett. 2007, 9, 3233. <https://doi.org/10.1021/ol071049d>
• Hassan Inas, Lauricella Robert, Tuccio Béatrice.: Preparation of N-aryl-ketonitrone spin traps. Open Chemistry 2006, 4. <https://doi.org/10.2478/s11532-006-0008-2>
• Ilias Md, Barman Dhiren C, Prajapati Dipak, Sandhu Jagir S: An indium mediated efficient chemoselective deoxygenation of N -oxides and nitrones. Tetrahedron Letters 2002, 43, 1877. <https://doi.org/10.1016/S0040-4039(02)00020-5>
• Khodot E. N., Petrova I. M., Anikin O. V., Chlenov I. E.: Preparation ofN-nitrohydroxylamines by substitutive nitration. Russ Chem Bull 1996, 45, 231. <https://doi.org/10.1007/BF01433769>
• Khodot E. N., Petrova I. V., Anikin O. V., Chlenov L. E.: Preparation ofN-nitrohydroxylamines by the substituting nitration method. Russ Chem Bull 1996, 45, 727. <https://doi.org/10.1007/BF01435817>
• Goti Andrea: Synthesis and cycloaddition reactions of N-methylcyclobutylideneamine N-oxide. Tetrahedron 1996, 52, 9187. <https://doi.org/10.1016/0040-4020(96)00469-3>
• Franco S., Merchán F. L., Merino P., Tejero T.: An Improved Synthesis of Ketonitrones. Synthetic Communications 1995, 25, 2275. <https://doi.org/10.1080/00397919508011783>
• Günter Aurich Hans, Frenzen Gerlinde, Rohr Markus G.: Formation of cycloadducts with trans-configurated ester groups from nitrones and dimethyl maleate. Tetrahedron 1994, 50, 7417. <https://doi.org/10.1016/S0040-4020(01)90471-5>
• Aurich Hans Günter, Franzke Michael, Kesselheim Hans Peter, Rohr Markus: Steric effects on regioselectivity in 1.3-Dipolar cycloaddition of C,N-dialyl nitrones with acceptor-substituted alkynes. Tetrahedron 1992, 48, 669. <https://doi.org/10.1016/S0040-4020(01)88127-8>
• Di Nunno L, Scilimati A: An efficient C2-homologation of aromatic aldehydes via 5-hydroxyisoxazolidines. Tetrahedron 1991, 47, 4121. <https://doi.org/10.1016/S0040-4020(01)86449-8>
• Hasnaoui A., El Messaoudi M., El Mouthadi M., Goupil J.‐M., Lavergne J.‐P.: Régio et périsélectivité de réactions de diels‐alder et des cycloadditions dipolaires‐1,3 avec une triazépine‐1,2,4: Approche théorique. Journal of Heterocyclic Chem 1988, 25, 453. <https://doi.org/10.1002/jhet.5570250219>
• Nour El-Din Ahmed M.: Charge-transfer complexes of nitrones—IV. Molecular complexes of N-alkyl nitrones with π-acceptors. Spectrochimica Acta Part A: Molecular Spectroscopy 1985, 41, 721. <https://doi.org/10.1016/0584-8539(85)80180-X>
• Funk Raymond L., Bolton Gary L., Daggett Joy Umstead, Hansen Marvin M., Horcher Linus H.M.: Intramolecular cycloaddition reactions of exocyclic nitrones. Tetrahedron 1985, 41, 3479. <https://doi.org/10.1016/S0040-4020(01)96702-X>
• Lebel Norman A., Balasubramanian N.: A convenient synthesis of nitrones by N-alkylation of O-trimethylsilyloximes. Tetrahedron Letters 1985, 26, 4331. <https://doi.org/10.1016/S0040-4039(00)98726-4>
• Kliegel Wolfgang, Nanninga Dierk: Borchelate von N ‐substituierten Hydroxamsäuren. Chem. Ber. 1983, 116, 2616. <https://doi.org/10.1002/cber.19831160718>
• Harpp David N., McDonald J.Gavin: Synthesis of thioamides from aldonitrones utilizing thiocarbonyl transfer reagents. Tetrahedron Letters 1983, 24, 4927. <https://doi.org/10.1016/S0040-4039(01)99813-2>
• Schenk C., Beekes M. L., de Boer Th. J.: C‐Nitroso compounds. Part XXXIII. Reaction of α‐chloronitrosoadamantane with Grignard reagents. Recl. Trav. Chim. Pays‐Bas 1980, 99, 246. <https://doi.org/10.1002/recl.19800990707>
• Inouye Yoshinobu, Hara Junko, Kakisawa Hiroshi: NOVEL E–Z EQUILIBRIUM OF N-ALKYL-α-ALKOXYCARBONYLNITRONE IN SOLUTION. Chemistry Letters 1980, 9, 1407. <https://doi.org/10.1246/cl.1980.1407>
• Schenk C., De Boer Th.J.: C-nitroso compounds—XXXI. Tetrahedron 1979, 35, 147. <https://doi.org/10.1016/0040-4020(79)85019-X>
• Pickart C.M., Jencks W.P.: Formation of stable anhydrides from CoA transferase and hydroxamic acids. Journal of Biological Chemistry 1979, 254, 9120. <https://doi.org/10.1016/S0021-9258(19)86819-9>
• Beckett Arnold H., Gibson G. Gordon: Stereochemistry of the Metabolic Incorporation of Oxygen into (+)- and (-)-N-Benzylamphetamine. Xenobiotica 1978, 8, 73. <https://doi.org/10.3109/00498257809060386>
• Kayen A. H. M., de Boer K., de Boer Th. J.: C‐nitroso compounds. Part XXVII. The lability of chlorine in (1‐chloroalkyl)nitroxides. Reaction with tri‐n‐butyltin hydride and nitric oxide. Recl. Trav. Chim. Pays‐Bas 1977, 96, 1. <https://doi.org/10.1002/recl.19770960102>
• Kayen A. H. M., de Boer Th. J.: C‐Nitroso compounds. Part XXVIII: Generation and reactivity of N‐(1‐chloroalkyl)nitrones obtained by reaction of diazoalkanes with gem‐chloronitroso compounds. Recl. Trav. Chim. Pays‐Bas 1977, 96, 8. <https://doi.org/10.1002/recl.19770960103>
• Kayen A. H. M., de Boer Th. J.: C‐Nitroso compounds. Part XXX. The mechanism of photolysis of chloro nitroso compounds; irradiation of 2‐chloro‐2‐nitrosoadamantane in methanol. Recl. Trav. Chim. Pays‐Bas 1977, 96, 237. <https://doi.org/10.1002/recl.19770960907>
• Lobo A.M., Prabhakar S., Fonseca M.T.C., Rodriguez A.M.B.: Protonation studies on n-methylhydroxamic acids. Tetrahedron Letters 1977, 18, 3167. <https://doi.org/10.1016/S0040-4039(01)83188-9>
• Kimura Kazuhiko, Niwa Hiroaki, Motoki Shinichi: Reactions of Thiocarboxylic Acids with Oximes and Nitrones. A New Synthesis of Thiones. Bulletin of the Chemical Society of Japan 1977, 50, 2751. <https://doi.org/10.1246/bcsj.50.2751>
• Kayen A. H. M., Bolsman Th. A. B. M., de Boer Th. J.: Generation of nitroxides with a chloro or nitro substituent in β‐position. Recl. Trav. Chim. Pays‐Bas 1976, 95, 14. <https://doi.org/10.1002/recl.19760950105>
• Coutts R. T., Dawe R., Beckett A. H.: A re-examination of the synthesis and some properties of thein vitro metabolite,N-hydroxyphenmetrazine. Biol. Mass Spectrom. 1975, 2, 137. <https://doi.org/10.1002/bms.1200020307>
• Gross M., Held P., Schubert H.: Synthese von Hydroxyguanidinen aus Chlorformamidinen und Oximen. J. Prakt. Chem. 1974, 316, 434. <https://doi.org/10.1002/prac.19743160311>
• Kadlubar F.F., McKee E.M., Ziegler D.M.: Reduced Pyridine nucleotide-dependent N-hydroxy amine oxidase and reductase activities of hepatic microsomes. Archives of Biochemistry and Biophysics 1973, 156, 46. <https://doi.org/10.1016/0003-9861(73)90339-1>
• Witanowski M., Stefaniak L., Januszewski H., Szymanski S., Webb G.A.: A nitrogen-14 NMR study of some oximes and their isomeric structures. Tetrahedron 1973, 29, 2833. <https://doi.org/10.1016/S0040-4020(01)93410-6>
• Kluiber R.W., Horrocks Jr. W.De W.: Spin delocalization in nitrones and imines coordinated to metal acethylacetonates. Inorganica Chimica Acta 1970, 4, 183. <https://doi.org/10.1016/S0020-1693(00)93269-9>
• Iwamura Michiko, Inamoto Naoki: Reactions of Nitrones with Free Radicals. I. Radical 1,3-Addition to Nitrones. Bulletin of the Chemical Society of Japan 1970, 43, 856. <https://doi.org/10.1246/bcsj.43.856>
• Zinner Gerwalt: Darstellung und Reaktionen einiger substituierter N‐Hydroxy‐urethane VII. Mitteilung über Hydroxylamin‐Derivate. Archiv der Pharmazie 1959, 292, 329. <https://doi.org/10.1002/ardp.19592920703>
• Horner Leopold, Steppan Hartmut: Studien Zum Ablauf Der Substitution XII. Umlagerung Und Thermischer Zerfall Acylierter Hydroxylamine. Justus Liebigs Ann. Chem. 1957, 606, 24. <https://doi.org/10.1002/jlac.19576060103>