Статті в журналах з теми "N-phenyl nitrones"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "N-phenyl nitrones".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.
Gallis, David E., James A. Warshaw, Bruce J. Acken та DeLanson R. Crist. "Electronic Nature of α-Methoxy, Amino, Cyano, and Mercapto Nitrones". Collection of Czechoslovak Chemical Communications 58, № 1 (1993): 125–41. http://dx.doi.org/10.1135/cccc19930125.
Повний текст джерелаMarano, Stefania, Cristina Minnelli, Lorenzo Ripani, Massimo Marcaccio, Emiliano Laudadio, Giovanna Mobbili, Adolfo Amici, Tatiana Armeni, and Pierluigi Stipa. "Insights into the Antioxidant Mechanism of Newly Synthesized Benzoxazinic Nitrones: In Vitro and In Silico Studies with DPPH Model Radical." Antioxidants 10, no. 8 (July 29, 2021): 1224. http://dx.doi.org/10.3390/antiox10081224.
Повний текст джерелаChamorro, Beatriz, Iwona E. Głowacka, Joanna Gotkowska, Rafał Gulej, Dimitra Hadjipavlou-Litina, Francisco López-Muñoz, José Marco-Contelles, Dorota G. Piotrowska, and María Jesús Oset-Gasque. "Nucleobase-Derived Nitrones: Synthesis and Antioxidant and Neuroprotective Activities in an In Vitro Model of Ischemia–Reperfusion." International Journal of Molecular Sciences 23, no. 6 (March 21, 2022): 3411. http://dx.doi.org/10.3390/ijms23063411.
Повний текст джерелаNakajima, Akira, Yuto Ueda, Nobuyuki Endoh, Kunihiko Tajima, and Keisuke Makino. "Electron spin resonance analysis of the oxidation reactions of nitrone type spin traps with gold(III) ion." Canadian Journal of Chemistry 83, no. 8 (August 1, 2005): 1178–84. http://dx.doi.org/10.1139/v05-132.
Повний текст джерелаRosselin, Marie, Fanny Choteau, Kamal Zéamari, Kevin M. Nash, Amlan Das, Robert Lauricella, Elisabeth Lojou, Béatrice Tuccio, Frederick A. Villamena та Grégory Durand. "Reactivities of Substituted α-Phenyl-N-tert-butyl Nitrones". Journal of Organic Chemistry 79, № 14 (3 липня 2014): 6615–26. http://dx.doi.org/10.1021/jo501121g.
Повний текст джерелаKliegel, W., L. Preu, Steven J. Rettig, and James Trotter. "Structural studies of organoboron compounds. XXI. Crystal and molecular structures of 3-(phenylmethylidene)-4-methyl-1-phenyl-2,6,7-trioxa-3-azonia-1-boratabicyclo-[2.2.2]octane and N-(4-nitrophenylmethylidene)-5-methyl-2-phenyl-1,3-dioxa-2-bora-5-cyclohexaneamine N-oxide." Canadian Journal of Chemistry 63, no. 2 (February 1, 1985): 509–15. http://dx.doi.org/10.1139/v85-083.
Повний текст джерелаMekheimer, Ramadan A., Khadijah Al-Zaydi, Mahmoud A. A. Ibrahim, Asma Al-Shamary, and Kamal Sadek. "Regio- and stereoselective 1,3-dipolar cycloaddition reactions of C-aryl (or hetaryl)-N-phenylnitrones to monosubstituted ylidene malononitriles and 4-benzylidene-2-phenyloxazol-5(4H)-one." Zeitschrift für Naturforschung B 72, no. 5 (May 1, 2017): 317–26. http://dx.doi.org/10.1515/znb-2016-0263.
Повний текст джерелаKliegel, Wolfgang, Jörg Metge, Steven J. Rettig, and James Trotter. "Aromatic aldonitrones of 2-(hydroxyamino)benzyl alcohol and their cyclic isomers. Crystal and molecular structures of a 1-hydroxy-1,2-dihydro-4H-3,1-benzoxazine, a boron chelate, and its parent nitrone ligand." Canadian Journal of Chemistry 76, no. 4 (April 1, 1998): 389–99. http://dx.doi.org/10.1139/v98-023.
Повний текст джерелаSuda, Kohji, Toshio Tsujimoto та Masashige Yamauchi. "13C and1H NMR of Arylnitrones. Substituent Effects of α-Phenyl-N-(p-substituted phenyl)nitrones". Bulletin of the Chemical Society of Japan 60, № 10 (жовтень 1987): 3607–11. http://dx.doi.org/10.1246/bcsj.60.3607.
Повний текст джерелаChamorro, Beatriz, David García-Vieira, Daniel Diez-Iriepa, Estíbaliz Garagarza, Mourad Chioua, Dimitra Hadjipavlou-Litina, Francisco López-Muñoz, José Marco-Contelles та María Jesús Oset-Gasque. "Synthesis, Neuroprotection, and Antioxidant Activity of 1,1′-Biphenylnitrones as α-Phenyl-N-tert-butylnitrone Analogues in In Vitro Ischemia Models". Molecules 26, № 4 (20 лютого 2021): 1127. http://dx.doi.org/10.3390/molecules26041127.
Повний текст джерелаDurand, Grégory, Marie Rosselin, Pierre-André Klein, Kamal Zéamari, Fanny Choteau та Béatrice Tuccio. "α-Phenyl-N-cyclohexyl Nitrones: Preparation and Use as Spin-Traps". Journal of Organic Chemistry 82, № 1 (20 грудня 2016): 135–42. http://dx.doi.org/10.1021/acs.joc.6b02262.
Повний текст джерелаDiez-Iriepa, Daniel, Beatriz Chamorro, Marta Talaván, Mourad Chioua, Isabel Iriepa, Dimitra Hadjipavlou-Litina, Francisco López-Muñoz, José Marco-Contelles та María Jesús Oset-Gasque. "Homo-Tris-Nitrones Derived from α-Phenyl-N-tert-butylnitrone: Synthesis, Neuroprotection and Antioxidant Properties". International Journal of Molecular Sciences 21, № 21 (26 жовтня 2020): 7949. http://dx.doi.org/10.3390/ijms21217949.
Повний текст джерелаDiez-Iriepa, Daniel, Damijan Knez, Stanislav Gobec, Isabel Iriepa, Cristóbal de los Ríos, Isaac Bravo, Francisco López-Muñoz, José Marco-Contelles та Dimitra Hadjipavlou-Litina. "Polyfunctionalized α-Phenyl-tert-butyl(benzyl)nitrones: Multifunctional Antioxidants for Stroke Treatment". Antioxidants 11, № 9 (31 серпня 2022): 1735. http://dx.doi.org/10.3390/antiox11091735.
Повний текст джерелаMöhrle, H., and M. Jeandrée. "Chinazolinderivate durch Cyclodehydrierung von N-(2-substituierten Aryl)-Piperidinen / Quinazoline Derivatives by Cyclodehydrogenation of N-(2-Substituted Aryl)-Piperidines." Zeitschrift für Naturforschung B 54, no. 12 (December 1, 1999): 1577–88. http://dx.doi.org/10.1515/znb-1999-1217.
Повний текст джерелаChamorro, Beatriz, Sara Izquierdo-Bermejo, María Dolores Martín-de-Saavedra, Francisco López-Muñoz, Mourad Chioua, José Marco-Contelles, and María Jesús Oset-Gasque. "Neuroprotective and Antioxidant Properties of Cholestero Nitrone ChN2 and QuinolylNitrone QN23 in an Experimental Model of Cerebral Ischemia: Involvement of Necrotic and Apoptotic Cell Death." Antioxidants 12, no. 7 (June 29, 2023): 1364. http://dx.doi.org/10.3390/antiox12071364.
Повний текст джерелаDowney, C. Wade, Erin N. Maxwell, and Danielle N. Confair. "Silyl triflate-accelerated additions of catalytically generated zinc acetylides to N-phenyl nitrones." Tetrahedron Letters 55, no. 35 (August 2014): 4959–61. http://dx.doi.org/10.1016/j.tetlet.2014.07.015.
Повний текст джерелаAl-Rawi, Jasmin M. A., Salim Y. Hanna та Amer A. Al-Rhman. "Solvent effects on the 1H NMR spectra of some α-(2-hydroxy-1-phenyl)-N-(4-substituted phenyl)nitrones". Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 51, № 14 (грудень 1995): 2585. http://dx.doi.org/10.1016/0584-8539(95)01484-5.
Повний текст джерелаJanzen, Edward G., and Coit M. Dubose. "Electron Impact Mass Spectra of Some Substituted C-Phenyl N-tert-Butyl Nitrones (PBN's)." Analytical Letters 26, no. 12 (December 1993): 2661–66. http://dx.doi.org/10.1080/00032719308017982.
Повний текст джерелаDeletraz, Anaïs, Béatrice Tuccio, Julien Roussel, Maud Combes, Catherine Cohen-Solal, Paul-Louis Fabre, Patrick Trouillas, Michel Vignes, Noelle Callizot та Grégory Durand. "Para-Substituted α-Phenyl-N-tert-butyl Nitrones: Spin-Trapping, Redox and Neuroprotective Properties". ACS Omega 5, № 48 (20 листопада 2020): 30989–99. http://dx.doi.org/10.1021/acsomega.0c03907.
Повний текст джерелаRosselin, Marie, Béatrice Tuccio, Pierre Pério, Frederick A. Villamena, Paul-Louis Fabre та Grégory Durand. "Electrochemical and Spin-Trapping Properties of para-substituted α-Phenyl-N-tert-butyl Nitrones". Electrochimica Acta 193 (березень 2016): 231–39. http://dx.doi.org/10.1016/j.electacta.2016.02.038.
Повний текст джерелаMarco-Contelles, José. "α-Phenyl-N-tert-Butylnitrone and Analogous α-Aryl-N-alkylnitrones as Neuroprotective Antioxidant Agents for Stroke". Antioxidants 13, № 4 (7 квітня 2024): 440. http://dx.doi.org/10.3390/antiox13040440.
Повний текст джерелаDowney, C. Wade, Erin N. Maxwell, and Danielle N. Confair. "ChemInform Abstract: Silyl Triflate-Accelerated Additions of Catalytically Generated Zinc Acetylides to N-Phenyl Nitrones." ChemInform 46, no. 6 (January 23, 2015): no. http://dx.doi.org/10.1002/chin.201506076.
Повний текст джерелаMarano, Stefania, Cristina Minnelli, Giovanna Mobbili, Emiliano Laudadio, and Pierluigi Stipa. "Synthesis and Evaluation of New Nitrone-Based Benzoxazinic Antioxidants." Medical Sciences Forum 2, no. 1 (November 30, 2020): 17. http://dx.doi.org/10.3390/cahd2020-08610.
Повний текст джерелаMatsunaga, Y., N. Kamiyama та Y. Nakayasu. "Liquid Crystalline Properties of Mixtures Composed of N-[4-(Dimethylamino)phenyl]- and N-(4-Nitrophenyl)-α-(4-alkoxyphenyl) nitrones". Molecular Crystals and Liquid Crystals 147, № 1 (січень 1987): 85–97. http://dx.doi.org/10.1080/00268948708084626.
Повний текст джерелаJayapradha, S. R., та S. Muthusubramanian. "Novel Rearrangement During the Reaction of Diethylmalonate with α-(5-Substituted 2-hydroxyphenyl)-N-phenyl Nitrones". Synthetic Communications 40, № 3 (6 січня 2010): 434–41. http://dx.doi.org/10.1080/00397910902985481.
Повний текст джерелаDeletraz, Anaïs, Kamal Zéamari, Kangyu Hua, Maud Combes, Frederick A. Villamena, Béatrice Tuccio, Noelle Callizot та Grégory Durand. "Substituted α-Phenyl and α-Naphthlyl-N-tert-butyl Nitrones: Synthesis, Spin-Trapping, and Neuroprotection Evaluation". Journal of Organic Chemistry 85, № 9 (8 квітня 2020): 6073–85. http://dx.doi.org/10.1021/acs.joc.0c00563.
Повний текст джерелаChang, Zen Yu, and Robert M. Coates. "Enantioselective synthesis of primary amines via Grignard additions to stereogenic N-(.alpha.-phenyl-.beta.-(benzyloxy)ethyl)nitrones." Journal of Organic Chemistry 55, no. 11 (May 1990): 3475–83. http://dx.doi.org/10.1021/jo00298a019.
Повний текст джерелаBulut, Gülen, Mehmet Oktav та Mert Ulgen. "The stability studies andin vitro hepatic microsomal metabolism of some α-phenyl-N-substituted nitrones in rats". European Journal of Drug Metabolism and Pharmacokinetics 29, № 4 (грудень 2004): 237–48. http://dx.doi.org/10.1007/bf03190606.
Повний текст джерелаAurich, Hans Günter, and Michael Soeberdt. "Darstellung enantiomerenreiner 3-Oxa-2,7-diazabicyclo[3.3.0]octane und ihre Umwandlung in andere bicyclische Ringsysteme/Preparation of Pure Enantiomeric 3-Oxa-2,7-diazabicyclo[3.3.0]octanes and their Conversion to Other Bicyclic Ring-Systems." Zeitschrift für Naturforschung B 54, no. 1 (January 1, 1999): 87–95. http://dx.doi.org/10.1515/znb-1999-0117.
Повний текст джерелаHaire, D. Larry, Uwe M. Oehler, H. Duane Goldman, Robert L. Dudley, and Edward G. Janzen. "The first 1H and 14N ENDOR spectra of an oxygen-centered radical adduct of DMPO-type nitrones." Canadian Journal of Chemistry 66, no. 9 (September 1, 1988): 2395–402. http://dx.doi.org/10.1139/v88-377.
Повний текст джерелаJayapradha, S. R., та S. Muthusubramanian. "ChemInform Abstract: Novel Rearrangement During the Reaction of Diethylmalonate with α-(5-Substituted 2-Hydroxyphenyl)-N-phenyl Nitrones." ChemInform 41, № 25 (22 червня 2010): no. http://dx.doi.org/10.1002/chin.201025052.
Повний текст джерелаMcCaig, Catherine, Paris Ataliotis, Anan Shtaya, Ayan S. Omar, A. Richard Green, Clive N. Kind, Anthony C. Pereira та ін. "Induction of the cell survival kinase Sgk1: A possible novel mechanism for α-phenyl-N-tert-butyl nitrone in experimental stroke". Journal of Cerebral Blood Flow & Metabolism 39, № 6 (20 грудня 2017): 1111–21. http://dx.doi.org/10.1177/0271678x17746980.
Повний текст джерелаHaire, D. Larry, Yashige Kotake, and Edward G. Janzen. "An EPR/ENDOR study of aminoxyls (nitroxides) capable of intramolecular bonding: hydroxyalkyl radical spin adducts of nitrones." Canadian Journal of Chemistry 66, no. 8 (August 1, 1988): 1901–11. http://dx.doi.org/10.1139/v88-307.
Повний текст джерелаUtenyshev, A. N., and S. M. Aldoshin. "Characteristic features of photochemical conversions ofC-(2-furyl-5-nitro)-N phenyl- andC,N-di(p-bromophenyl)nitrones in liquid and crystal phases." Russian Chemical Bulletin 45, no. 11 (November 1996): 2529–34. http://dx.doi.org/10.1007/bf01431109.
Повний текст джерелаAmutha, Chinnadurai, Sivaperuman Saravanan, and Shanmugam Muthusubramanian. "ChemInform Abstract: Acetic Anhydride Induced Rearrangement and Grignard Addition on C-Phenyl-N-(1-methyl-2-aryl)ethyl Nitrones." ChemInform 44, no. 35 (August 8, 2013): no. http://dx.doi.org/10.1002/chin.201335075.
Повний текст джерелаGosh, Anindita, Avijit Banerji, and Julie Banerji. "ChemInform Abstract: 1,3-Dipolar Cycloadditions. Part 28. Selective 1,3-Dipolar Cycloadditions of C-Aryl-N-Phenyl Nitrones to Arylidene Acetones." ChemInform 46, no. 17 (April 2015): no. http://dx.doi.org/10.1002/chin.201517181.
Повний текст джерелаLasri, Jamal, Naser Eltaher Eltayeb, Matti Haukka, and Yousef Alghamdi. "Crystal and molecular structure studies of (Z)-N-methyl-C-4-substituted phenyl nitrones by XRD, DFT, FTIR and NMR methods." Journal of Molecular Structure 1128 (January 2017): 70–78. http://dx.doi.org/10.1016/j.molstruc.2016.08.058.
Повний текст джерелаChakraborty, Bhaskar, Prawin Kumar Sharma, Neelam Rai, Saurav Kafley та Manjit Chhetri. "α-N-Methyl/phenyl furan derivatives as dipolarophiles for synthesis of spiro isoxazolidine derivatives with α-chloro and simple nitrones". Journal of Chemical Research 34, № 3 (1 березня 2010): 147–50. http://dx.doi.org/10.3184/030823410x12675422347141.
Повний текст джерелаChakraborty, Bhaskar, Prawin Kumar Sharma, Neelam Rai, Saurav Kafley та Manjit Chhetri. "ChemInform Abstract: α-N-Methyl/Phenyl Furan Derivatives as Dipolarophiles for Synthesis of Spiro Isoxazolidine Derivatives with α-Chloro and Simple Nitrones." ChemInform 41, № 36 (12 серпня 2010): no. http://dx.doi.org/10.1002/chin.201036128.
Повний текст джерелаUTENYSHEV, A. N., and S. M. ALDOSHIN. "ChemInform Abstract: Specific Features of the Photochemical Conversion of C-(5-Nitro-2- furyl)-N-phenyl- and C,N-Di(p-bromophenyl)nitrones in Liquid and Crystal Phases." ChemInform 28, no. 16 (August 4, 2010): no. http://dx.doi.org/10.1002/chin.199716071.
Повний текст джерелаEskandari, Khalil, Bahador Karami та Saeed Khodabakhshi. "An Unexpected Catalytic Synthesis of Novel and Known Bis(Pyrazolyl) Methanes by the use of α-aryl-N-phenyl Nitrones in Aqueous Media". Journal of Chemical Research 38, № 10 (жовтень 2014): 600–603. http://dx.doi.org/10.3184/174751914x14114871789226.
Повний текст джерелаEskandari, Khalil, Bahador Karami та Saeed Khodabakhshi. "ChemInform Abstract: An Unexpected Catalytic Synthesis of Novel and Known Bis(pyrazolyl) Methanes by the Use of α-Aryl-N-phenyl Nitrones in Aqueous Media." ChemInform 46, № 19 (23 квітня 2015): no. http://dx.doi.org/10.1002/chin.201519162.
Повний текст джерелаChakraborty, Bhaskar, and Esmita Chettri. "Synthesis of Some Novel Class of Regioselective Spiro Isoxazolidine Derivatives via 1,3-Dipolar Cycloaddition Reaction of N- Benzyl-C- fluoro-substituted Phenyl Nitrones in Ionic Liquid." Journal of Heterocyclic Chemistry 55, no. 5 (March 12, 2018): 1157–65. http://dx.doi.org/10.1002/jhet.3148.
Повний текст джерелаvan Eijk, Peter J. S. S., Willem P. Trompenaars, David N. Reinhoudt та Sybolt Harkema. "Reaction of four-membered cyclic nitrones with acetyl chlorideα. X-Ray crystal structures of 2-[(acetyloxy)amino]-N,N-diethyl-2-methyl-4-oxo-3-phenylpentanamide and 1-acetyl-3-chloro-N, N-diethyl-2-methyl-4-methylene-3-phenyl-2-azetidinecarboxamide". Recueil des Travaux Chimiques des Pays-Bas 107, № 2 (2 вересня 2010): 52–62. http://dx.doi.org/10.1002/recl.19881070204.
Повний текст джерелаZhang, Yong-Kang, and Kirk R. Maples. "Synthesis and EPR Evaluation of the Nitrone PBN-[tert-13C] for Spin Trapping Competition." Zeitschrift für Naturforschung B 57, no. 1 (January 1, 2002): 127–32. http://dx.doi.org/10.1515/znb-2002-0116.
Повний текст джерелаRehorek, Detlef, Edward G. Janzen, and Yashige Kotake. "On the spin trapping of chlorine atoms. Competition from chloride ions." Canadian Journal of Chemistry 69, no. 7 (July 1, 1991): 1131–33. http://dx.doi.org/10.1139/v91-167.
Повний текст джерелаBouwman, Jordy, Andras Bodi, and Patrick Hemberger. "Nitrogen matters: the difference between PANH and PAH formation." Physical Chemistry Chemical Physics 20, no. 47 (2018): 29910–17. http://dx.doi.org/10.1039/c8cp05830j.
Повний текст джерелаHeinemann, Frank W., Helmut Hartung, and Nadja Maier. "Kristall- und Molekülstruktur von 2-[3-(N,N-Diethylammonium)propylimino]-2-phenyl-dithioacetat / Crystal and Molecular Structure of 2-[3-(N,N-Diethylammonium)propylimino]-2-phenyl-dithioacetate." Zeitschrift für Naturforschung B 50, no. 1 (January 1, 1995): 81–85. http://dx.doi.org/10.1515/znb-1995-0116.
Повний текст джерелаLu, Guifen, Xiufeng Zhang, Xu Cai, Yuanyuan Fang, Min Zhu, Weihua Zhu, Zhongping Ou, and Karl M. Kadish. "Synthesis, structural characterization and protonation/deprotonation of hydroxyl-substituted free-base tetraphenylporphyrins in nonaqueous media." Journal of Porphyrins and Phthalocyanines 17, no. 10 (September 9, 2013): 941–53. http://dx.doi.org/10.1142/s1088424613500557.
Повний текст джерелаShchepina, Nadezhda E., Viktor V. Avrorin, Gennady A. Badun, Scott B. Lewis, and Sergey N. Shurov. "New Way of Direct Nitrogen Atom Phenylation in Quinoline Derivatives." ISRN Organic Chemistry 2012 (July 3, 2012): 1–4. http://dx.doi.org/10.5402/2012/526867.
Повний текст джерела