Статті в журналах з теми "Hydroxylamine derivatives"
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Reissig, Hans-Ulrich, and Reinhold Zimmer. "Cyclizations of Alkoxyallenes: Mechanisms, Intermediates, Products – A Personal Account on Solved and Unsolved Problems with Unique Allene Building Blocks." Synthesis 49, no. 15 (June 6, 2017): 3291–302. http://dx.doi.org/10.1055/s-0036-1588846.
Повний текст джерелаRehse, Klaus, and Tawfig Shahrouri. "Hydroxylamine Derivatives." Archiv der Pharmazie 331, no. 11 (November 1998): 365–67. http://dx.doi.org/10.1002/(sici)1521-4184(199811)331:11<365::aid-ardp365>3.0.co;2-n.
Повний текст джерелаTorruellas, Carilyn, Fu-Lian Hsu, and Andrew J. Walz. "Synthesis of N-Pyridyl Hydroxylamines via Copper-Catalyzed Cross-Coupling." Synthesis 51, no. 15 (May 15, 2019): 2891–96. http://dx.doi.org/10.1055/s-0037-1611836.
Повний текст джерелаPískala, Alois, Naeem B. Hanna, Milena Masojídková, Pavel Fiedler та Ivan Votruba. "Synthesis of N4-Amino and N4-Hydroxy Derivatives of 5-Azacytidine. A Facile Rearrangement of the N4-Amino Derivative to 5-(3-β-D-Ribofuranosylureido)-1H-1,2,4-triazole". Collection of Czechoslovak Chemical Communications 69, № 4 (2004): 905–17. http://dx.doi.org/10.1135/cccc20040905.
Повний текст джерелаBaldauf, Simon, and Jeffrey Bode. "Synthesis and Evaluation of Cyclic Acetals of Serine Hydroxylamine for Amide-Forming KAHA Ligations." Synthesis 51, no. 05 (January 7, 2019): 1273–83. http://dx.doi.org/10.1055/s-0037-1611635.
Повний текст джерелаVeits, Gesine K., Donald R. Wenz, Leoni I. Palmer, André H. St. Amant, Jason E. Hein, and Javier Read de Alaniz. "Cascade rearrangement of furylcarbinols with hydroxylamines: practical access to densely functionalized cyclopentane derivatives." Organic & Biomolecular Chemistry 13, no. 31 (2015): 8465–69. http://dx.doi.org/10.1039/c5ob00944h.
Повний текст джерелаSpooren, Anita AMG, and Chris TA Evelo. "Only the glutathione dependent antioxidant enzymes are inhibited by haematotoxic hydroxylamines." Human & Experimental Toxicology 17, no. 10 (October 1998): 554–59. http://dx.doi.org/10.1177/096032719801701005.
Повний текст джерелаGuy, Michelle, Sally Freeman, John Alder, and Simon Brandt. "The Henry reaction: spectroscopic studies of nitrile and hydroxylamine by-products formed during synthesis of psychoactive phenylalkylamines." Open Chemistry 6, no. 4 (December 1, 2008): 526–34. http://dx.doi.org/10.2478/s11532-008-0054-z.
Повний текст джерелаHashem, Heba E., and Ahmed M. Abo-Bakr. "Synthesis of Some New 1,2,4-Triazine and 1,2,5-Oxadiazine Derivatives with Antimicrobial Activity." Heteroatom Chemistry 2019 (September 25, 2019): 1–7. http://dx.doi.org/10.1155/2019/2326514.
Повний текст джерелаAnyun, Zhang, Hu Jingxin, Zhang Xianye, and Wang Fangding. "Hydroxylamine derivatives in Purex Process." Journal of Radioanalytical and Nuclear Chemistry 230, no. 1-2 (April 1998): 235–39. http://dx.doi.org/10.1007/bf02387470.
Повний текст джерелаM.G., Assy, Abdalha A.A., and Abdel Aziz A.E. "Synthesis and Antimicrobial Evaluation of Some New Benzoxazinone and Quinazolinone Derivatives." JOURNAL OF ADVANCES IN CHEMISTRY 8, no. 1 (December 20, 2016): 1491–99. http://dx.doi.org/10.24297/jac.v8i1.4030.
Повний текст джерелаEl Ashry, El Sayed H., Laila Fathy Awad, Mohamed Nabil Abd Al Moaty, and Omayma Kh Bdeewy. "A novel trans-amination process in 3-arylamino- 5,5-dimethylcyclohex-2-en-1-one with nucleophiles and antimicrobial activity of selected products." Mediterranean Journal of Chemistry 7, no. 6 (January 7, 2019): 452–62. http://dx.doi.org/10.13171/mjc7619019140eshea.
Повний текст джерелаEl-Ghanam, Abdel Moneim. "New Route Synthesis of Styryl Pyrones: High Yield Synthesis, Reactions and Spectral Properties of 2-Phenyl-6-Styryl-4-Pyrones." Journal of Chemical Research 2005, no. 10 (October 2005): 654–56. http://dx.doi.org/10.3184/030823405774663101.
Повний текст джерелаMohammed, Jihad Haji, AKRAM Noori Mohammed QADDO, Nabaz Abdulmajeed Mohammad Salih, and Faeza Burhan Omar. "The Synthesis of Some Imine Derivatives via Condensation Reactions between Some Aromatic Phenylhydroxylamine Derivatives with Glyoxylic Acid and the Study of their biological activity." Tikrit Journal of Pure Science 28, no. 6 (December 25, 2023): 34–41. http://dx.doi.org/10.25130/tjps.v28i6.1411.
Повний текст джерелаSchmid, G. H., K. P. Bader, A. Radunz, C. J. van Assche, N. Reinier, and B. Courtiade. "Effect of Hydroxylamine Derivatives on Photorespiration in the Tobacco Aurea Mutant Nicotiana tabacum Su/su." Zeitschrift für Naturforschung C 42, no. 7-8 (August 1, 1987): 965–69. http://dx.doi.org/10.1515/znc-1987-7-839.
Повний текст джерелаMöhrle, Hans, and Robert Nießen. "Umsetzung von N-Alkylpyridinium-Salzen mit Hydroxylamin / Reaction of N-Alkylpyridinium Salts with Hydroxylamine." Zeitschrift für Naturforschung B 55, no. 5 (May 1, 2000): 434–42. http://dx.doi.org/10.1515/znb-2000-0514.
Повний текст джерелаZhou, Qishun, Bao Vu Ngoc, Grazyna Leszczynska, Jean-Luc Stigliani, and Geneviève Pratviel. "Oxidation of 5-methylaminomethyl uridine (mnm5U) by Oxone Leads to Aldonitrone Derivatives." Biomolecules 8, no. 4 (November 14, 2018): 145. http://dx.doi.org/10.3390/biom8040145.
Повний текст джерелаKirby, Georgina, Laurence Grimaud, Maxime R. Vitale, Guillaume Prestat, and Farouk Berhal. "Iron(ii)-catalyzed intermolecular aziridination of alkenes employing hydroxylamine derivatives as clean nitrene sources." Green Chemistry 23, no. 23 (2021): 9428–32. http://dx.doi.org/10.1039/d1gc03495b.
Повний текст джерелаFallon, Gary D., Saba Jahangiri, Andris J. Liepa, and Ruth C. J. Woodgate. "N,N-Dialkyl (N'-Chlorosulfonyl)chloroformamidines in Heterocyclic Synthesis. I. The Preparation of [1,2,3,5]Thiatriazole and [1,3,2,4]Oxathiadiazole Derivatives." Australian Journal of Chemistry 58, no. 5 (2005): 332. http://dx.doi.org/10.1071/ch04295.
Повний текст джерелаMiyakoshi, Takeru, and Hiroyuki Konno. "Improved synthesis of 2,4,6-trialkylpyridines from 1,5-diketoalkanes: the total synthesis of Anibamine." Organic & Biomolecular Chemistry 17, no. 11 (2019): 2896–905. http://dx.doi.org/10.1039/c8ob02723d.
Повний текст джерелаChen, N., and J. Xie. "N–O linkage in carbohydrates and glycoconjugates." Organic & Biomolecular Chemistry 14, no. 47 (2016): 11028–47. http://dx.doi.org/10.1039/c6ob00120c.
Повний текст джерелаMöhrle, H., and R. Nießen. "Reaktionen von Isochinolinium-Salzen mit Hydroxylamin-Derivaten, 1. Mitteilung. N-(Nitrophenyl)-substituierte Verbindungen/Reactions of Isoquinolinium Salts with Hydroxylamine Derivatives, 1st Communication. N-(Nitrophenyl) Substituted Compounds." Zeitschrift für Naturforschung B 54, no. 2 (February 1, 1999): 225–33. http://dx.doi.org/10.1515/znb-1999-0211.
Повний текст джерелаAbdallah, Tayseer A., Abdellatif M. Salaheldin, and Naglaa F. Radwan. "Studies With Enamines: Synthesis and Reactivity of 4-Nitrophenyl-1-piperidinostyrene. Synthesis of Pyridazine, Oxadiazole, 1,2,3-Triazole and 4-Aminopyrazole Derivatives." Zeitschrift für Naturforschung B 62, no. 2 (February 1, 2007): 261–66. http://dx.doi.org/10.1515/znb-2007-0218.
Повний текст джерелаAmr, Abdel-Galil E. "Synthesis of Some New Linear and Chiral Macrocyclic Pyridine Carbazides as Analgesic and Anticonvulsant Agents." Zeitschrift für Naturforschung B 60, no. 9 (September 1, 2005): 990–98. http://dx.doi.org/10.1515/znb-2005-0914.
Повний текст джерелаPouzar, Vladimír, та Ivan Černý. "17-(O-(2-Carboxyethyl)oxime) Derivatives of Androstanes of 3-Hydroxy-5α-, -5β-, -5-ene and 3-Oxo-4-ene Series". Collection of Czechoslovak Chemical Communications 60, № 1 (1995): 137–49. http://dx.doi.org/10.1135/cccc19950137.
Повний текст джерелаZhang, Guangyu, and Jiaxi Xu. "[3,3] Sigmatropic Shifts and Applications of Hydroxylamine Derivatives." Chinese Journal of Organic Chemistry 41, no. 8 (2021): 3002. http://dx.doi.org/10.6023/cjoc202103022.
Повний текст джерелаRaban, Morton, Van A. Martin, and Leslie Craine. "Torsional barriers in quinolinone hydroxylamine and sulfenamide derivatives." Journal of Organic Chemistry 55, no. 14 (July 1990): 4311–16. http://dx.doi.org/10.1021/jo00301a020.
Повний текст джерелаHacking, M. A. P. J., F. van Rantwijk, and R. A. Sheldon. "Lipase catalysed acylation of hydroxylamine and hydrazine derivatives." Journal of Molecular Catalysis B: Enzymatic 11, no. 4-6 (January 2001): 315–21. http://dx.doi.org/10.1016/s1381-1177(00)00144-2.
Повний текст джерелаOvakimyan, M. Zh, S. K. Barsegyan, N. M. Kikoyan, and M. G. Indzhikyan. "Reactions of Phosphonioalkyl Derivatives of Phenylhydrazine and Hydroxylamine." Russian Journal of General Chemistry 75, no. 7 (July 2005): 1069–73. http://dx.doi.org/10.1007/s11176-005-0369-9.
Повний текст джерелаČerný, Ivan, Helena Havlíková, Martin Hill, Richard Hampl та Vladimír Pouzar. "Synthetic Approach to 5α-Pregnanolone 19-[O-(Carboxymethyl)oxime] Derivatives". Collection of Czechoslovak Chemical Communications 69, № 9 (2004): 1805–17. http://dx.doi.org/10.1135/cccc20041805.
Повний текст джерелаPatel, Anjan, Andreas Hofinger та Thomas Rosenau. "Synthesis and analytical characterization of monomeric N-oxidized derivatives of α-tocopheramine". Monatshefte für Chemie - Chemical Monthly 152, № 8 (серпень 2021): 959–66. http://dx.doi.org/10.1007/s00706-021-02805-8.
Повний текст джерелаSun, Bin, Shi Yin, Xiaohui Zhuang, Can Jin, and Weike Su. "Selectfluor-induced C(sp2)–O coupling reaction of N-substituted anilines with hydroxylamine derivatives." Organic & Biomolecular Chemistry 16, no. 33 (2018): 6017–24. http://dx.doi.org/10.1039/c8ob01348a.
Повний текст джерелаPlešek, Jaromír, Farzaneh Hosseinpour Rajabi, Veena Vangani та Jiří Fusek. "Constitution and Properties of the 8,8'-μ-(H2NO)=(1,2-C2B9H10)2-3-Co Bridged Cobaltaborane". Collection of Czechoslovak Chemical Communications 59, № 6 (1994): 1326–36. http://dx.doi.org/10.1135/cccc19941326.
Повний текст джерелаSlavíková, Tereza, Vladimír Pouzar, and Ivan Černý. "Syntheses of Steroid O-(3-Carboxypropyl)oximes." Collection of Czechoslovak Chemical Communications 62, no. 3 (1997): 457–70. http://dx.doi.org/10.1135/cccc19970457.
Повний текст джерелаStrashnova, S. B., O. V. Avramenko, M. N. Zhuk, O. V. Kovalchukova, P. V. Strashnov, and B. E. Zaitsev. "Synthesis and Study of Complexes of Copper(II), Zinc, Cobalt(II) and Nickel(II) with Nitrofluorenylidene-9-Amino(Imino) Derivatives." Chemistry Journal of Moldova 4, no. 2 (December 2009): 68–71. http://dx.doi.org/10.19261/cjm.2009.04(2).09.
Повний текст джерелаIvanov, Maksim A., Elena V. Antonova, Aleksey V. Maksimov, Lyudmila K. Pigusova, Evgenii F. Belanov, and Lyudmila A. Aleksandrova. "New N4-Hydroxycytidine Derivatives: Synthesis and Antiviral Activity." Collection of Czechoslovak Chemical Communications 71, no. 7 (2006): 1099–106. http://dx.doi.org/10.1135/cccc20061099.
Повний текст джерелаKhomutov, M. A., J. Weisell, M. Hyvönen, T. A. Keinänen, J. Vepsäläinen, L. Alhonen, A. R. Khomutov, and S. N. Kochetkov. "Hydroxylamine derivatives for regulation of spermine and spermidine metabolism." Biochemistry (Moscow) 78, no. 13 (December 2013): 1431–46. http://dx.doi.org/10.1134/s0006297913130051.
Повний текст джерелаTan, Fen, Ping Zheng, and You-Quan Zou. "Highly Selective Asymmetric Hydrogenation of Oximes to Hydroxylamine Derivatives." Chem 6, no. 7 (July 2020): 1517–19. http://dx.doi.org/10.1016/j.chempr.2020.06.025.
Повний текст джерелаAltenburger, J. M., C. Mioskowski, H. d'Orchymont, D. Schirlin, C. Schalk, and C. Tarnus. "Useful hydroxylamine derivatives for the synthesis of hydroxamic acids." Tetrahedron Letters 33, no. 35 (August 1992): 5055–58. http://dx.doi.org/10.1016/s0040-4039(00)61187-5.
Повний текст джерелаDeepa, Boppana, Natesan Balasubramanian, and Karachalacherevu Seetharamiah Nagaraja. "Spectrophotometric Determination of Hydroxylamine and Its Derivatives in Pharmaceuticals." CHEMICAL & PHARMACEUTICAL BULLETIN 52, no. 12 (2004): 1473–75. http://dx.doi.org/10.1248/cpb.52.1473.
Повний текст джерелаLiang, Guyan, J. Phillip Bowen, and James A. Bentley. "Molecular mechanics (MM3) parameterization of hydroxylamine and methyl derivatives." Journal of Computational Chemistry 15, no. 8 (August 1994): 866–74. http://dx.doi.org/10.1002/jcc.540150808.
Повний текст джерелаDworak, Claudia, Stefan Kopeinig, Helmuth Hoffmann, and Robert Liska. "Photoinitiating monomers based on di- and triacryloylated hydroxylamine derivatives." Journal of Polymer Science Part A: Polymer Chemistry 47, no. 2 (January 15, 2009): 392–403. http://dx.doi.org/10.1002/pola.23156.
Повний текст джерелаS. AL-Rawi, Muna, Huda A. Hassan, Dheefaf F. Hassan та Ismaeel Y. Majeed. "New Series of Substituted Heterocyclics Derived from α , β – Unsaturated Ketone and Their Cytotoxic Activity Tumor Cell Lines". Oriental Journal of Chemistry 34, № 6 (10 листопада 2018): 2826–31. http://dx.doi.org/10.13005/ojc/340620.
Повний текст джерелаČerný, Ivan, Tereza Slavíková та Vladimír Pouzar. "Synthesis of (15E)-17β-hydroxy-5α-androstane-3,15-dione 15-[O-(Carboxymethyl)]oxime, New Hapten for Dihydrotestosterone (17β-hydroxy-5α-androstan-3-one)". Collection of Czechoslovak Chemical Communications 62, № 10 (1997): 1642–49. http://dx.doi.org/10.1135/cccc19971642.
Повний текст джерелаEl Mahmoudi, Ayoub, Khalid Karrouchi, Hamza Tachallait, and Khalid Bougrin. "Ultrasound Assisted One-Pot Synthesis of Novel 3-(Aryl)-5-((4-(phenyldiazenyl)phenoxy)methyl)isoxazolines in Water." Molbank 2022, no. 4 (December 17, 2022): M1529. http://dx.doi.org/10.3390/m1529.
Повний текст джерелаSafaei-Ghomi, Javad, and Ali Ghasemzadeh. "Synthesis of some 3,5-diarylisoxazoline derivatives in ionic liquids media." Journal of the Serbian Chemical Society 77, no. 6 (2012): 733–39. http://dx.doi.org/10.2298/jsc110831001s.
Повний текст джерелаPatil, Sachin V. "SYNTHESIS AND ANTIMICROBIAL EVALUATION OF SOME NEW BENZTHIAZOLE OXIME ETHER DERIVATIVES." Journal of Medical pharmaceutical and allied sciences 11, no. 6 (November 15, 2021): 47–50. http://dx.doi.org/10.22270/jmpas.v10i6.1916.
Повний текст джерелаKotwal, Urmila, Archana Tiwari, and Shweta Choudhary. "Synthesis, Characterization and Antimicrobial Activity of Isoxazoline Derivatives." International Journal of Pharmaceutical Sciences and Medicine 7, no. 11 (November 30, 2022): 107–20. http://dx.doi.org/10.47760/ijpsm.2022.v07i11.008.
Повний текст джерелаDommaraju, Yuvaraj, Somadrita Borthakur, and Dipak Prajapati. "l-Proline-Catalysed One-Pot aza-Diels–Alder Reaction in Water: Regioselective Synthesis of Spiro(isoxazolo[5,4-b]pyridine-5,5′-pyrimidine) Derivatives." Synlett 29, no. 09 (March 20, 2018): 1195–98. http://dx.doi.org/10.1055/s-0036-1591949.
Повний текст джерелаEl-Sharkawy, Karam A., Mohammed Al Bratty, Hassan A. Alhazmi, and Asim Najmi. "Design, synthesis, and biological activities of novel thiophene, pyrimidine, pyrazole, pyridine, coumarin and isoxazole: Dydrogesterone derivatives as antitumor agents." Open Chemistry 19, no. 1 (January 1, 2021): 322–37. http://dx.doi.org/10.1515/chem-2021-0028.
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