Статті в журналах з теми "Iminoquinone"
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Dong, Yu, Zhong-Hui Li, Bing He, Hui Jiang, Xiang-Long Chen, Ji-Xian Ye, Qiang Zhou, Long-Sen Gao, Qi-Qi Luo, and Zhi-Chuan Shi. "Silver-Catalyzed One-Pot Biarylamination of Quinones with Arylamines: Access to N-Arylamine-Functionalized p-Iminoquinone Derivatives." Synthesis 54, no. 09 (February 7, 2022): 2242–50. http://dx.doi.org/10.1055/s-0041-1737340.
Повний текст джерелаBouchard, Luc, Ian Marcotte, Jean Marc Chapuzet, and Jean Lessard. "Electroreduction of 1-methyl 5-nitroindole, 5-nitrobenzofurane, and 5-nitrobenzothiophene in acidic and basic hydroorganic media: Generation and trapping of iminoquinone-type intermediates and electrosynthesis of ring-substituted amino derivatives." Canadian Journal of Chemistry 81, no. 10 (October 1, 2003): 1108–18. http://dx.doi.org/10.1139/v03-149.
Повний текст джерелаKlementyeva, Svetlana V., Anton N. Lukoyanov, Mikhail Yu Afonin, Max Mörtel, Anton I. Smolentsev, Pavel A. Abramov, Alyona A. Starikova, Marat M. Khusniyarov, and Sergey N. Konchenko. "Europium and ytterbium complexes with o-iminoquinonato ligands: synthesis, structure, and magnetic behavior." Dalton Transactions 48, no. 10 (2019): 3338–48. http://dx.doi.org/10.1039/c8dt04849e.
Повний текст джерелаChandrasekar, Selvaraj, and Govidasamy Sekar. "An efficient synthesis of iminoquinones by a chemoselective domino ortho-hydroxylation/oxidation/imidation sequence of 2-aminoaryl ketones." Organic & Biomolecular Chemistry 14, no. 11 (2016): 3053–60. http://dx.doi.org/10.1039/c5ob02659h.
Повний текст джерелаBamford, Karlee L., Lauren E. Longobardi, Lei Liu, Stefan Grimme та Douglas W. Stephan. "FLP reduction and hydroboration of phenanthrene o-iminoquinones and α-diimines". Dalton Transactions 46, № 16 (2017): 5308–19. http://dx.doi.org/10.1039/c7dt01024a.
Повний текст джерелаKamitanaka, Tohru, Koji Morimoto, Toshifumi Dohi, and Yasuyuki Kita. "Controlled-Coupling of Quinone Monoacetals by New Activation Methods: Regioselective Synthesis of Phenol-Derived Compounds." Synlett 30, no. 10 (March 25, 2019): 1125–43. http://dx.doi.org/10.1055/s-0037-1611735.
Повний текст джерелаConboy, Darren, and Fawaz Aldabbagh. "6-Imino-1,2,3,4,8,9,10,11-octahydropyrido[1,2-a]pyrido[1′,2′:1,2]imidazo[4,5-f]benzimidazole-13-one: Synthesis and Cytotoxicity Evaluation." Molbank 2020, no. 1 (March 5, 2020): M1118. http://dx.doi.org/10.3390/m1118.
Повний текст джерелаJohannissen, Linus O., Nigel S. Scrutton, and Michael J. Sutcliffe. "The enzyme aromatic amine dehydrogenase induces a substrate conformation crucial for promoting vibration that significantly reduces the effective potential energy barrier to proton transfer." Journal of The Royal Society Interface 5, suppl_3 (May 21, 2008): 225–32. http://dx.doi.org/10.1098/rsif.2008.0068.focus.
Повний текст джерелаLiu, Liu, Kun Chen, Wen-Zhen Wu, Peng-Fei Wang, Hang-Yu Song, Hongbin Sun, Xiaoan Wen, and Qing-Long Xu. "Organocatalytic Para-Selective Amination of Phenols with Iminoquinone Monoacetals." Organic Letters 19, no. 14 (July 11, 2017): 3823–26. http://dx.doi.org/10.1021/acs.orglett.7b01700.
Повний текст джерелаErshova, I. V., and A. V. Piskunov. "Complexes of Group III Metals based on o-Iminoquinone Ligands." Russian Journal of Coordination Chemistry 46, no. 3 (March 2020): 154–77. http://dx.doi.org/10.1134/s1070328420030021.
Повний текст джерелаMatson, Ellen M., Sebastian M. Franke, Nickolas H. Anderson, Timothy D. Cook, Phillip E. Fanwick, and Suzanne C. Bart. "Radical Reductive Elimination from Tetrabenzyluranium Mediated by an Iminoquinone Ligand." Organometallics 33, no. 8 (April 7, 2014): 1964–71. http://dx.doi.org/10.1021/om4012104.
Повний текст джерелаKovacic, Peter, and Ratnasamy Somanathan. "Mechanism of Anesthetic Toxicity: Metabolism, Reactive Oxygen Species, Oxidative Stress, and Electron Transfer." ISRN Anesthesiology 2011 (January 17, 2011): 1–10. http://dx.doi.org/10.5402/2011/402906.
Повний текст джерелаXu, Bin, Anjie Ma, Teng Jia, Zhiqiang Hao, Wei Gao, and Ying Mu. "Synthesis and structural characterization of iron complexes bearing N-aryl-phenanthren-o-iminoquinone ligands." Dalton Transactions 45, no. 44 (2016): 17966–73. http://dx.doi.org/10.1039/c6dt03572h.
Повний текст джерелаMondal, Manas Kumar, and Chandan Mukherjee. "An unprecedented one-step synthesis of octahedral Cu(ii)-bis(iminoquinone) complexes and their reactivity with NaBH4." Dalton Transactions 45, no. 34 (2016): 13532–40. http://dx.doi.org/10.1039/c6dt02443b.
Повний текст джерелаMeshcheryakova, I. N., O. Yu Trofimova, N. O. Druzhkov, K. I. Pashanova, I. A. Yakushev, P. V. Dorovatovskii, M. N. Khrizanforov, Yu G. Budnikova, R. R. Aisin, and A. V. Piskunov. "Magnesium and Nickel Complexes with Bis(p-iminoquinone) Redox-Active Ligand." Russian Journal of Coordination Chemistry 47, no. 5 (May 2021): 307–18. http://dx.doi.org/10.1134/s1070328421050043.
Повний текст джерелаEzell, Scharri J., Haibo Li, Hongxia Xu, Xiangrong Zhang, Evrim Gurpinar, Xu Zhang, Elizabeth R. Rayburn, et al. "Preclinical Pharmacology of BA-TPQ, a Novel Synthetic Iminoquinone Anticancer Agent." Marine Drugs 8, no. 7 (July 13, 2010): 2129–41. http://dx.doi.org/10.3390/md8072129.
Повний текст джерелаMure, Minae, Shinobu Itoh, and Yoshiki Ohshiro. "Preparation and characterization of iminoquinone and aminophenol derivatives of coenzyme PQQ." Tetrahedron Letters 30, no. 49 (January 1989): 6875–78. http://dx.doi.org/10.1016/s0040-4039(01)93377-5.
Повний текст джерелаAbakumov, G. A., V. K. Cherkasov, A. V. Piskunov, I. N. Meshcheryakova, A. V. Maleeva, A. I. Poddel’skii, and G. K. Fukin. "Zinc molecular complexes with sterically hindered o-quinone and o-iminoquinone." Doklady Chemistry 427, no. 1 (July 2009): 168–71. http://dx.doi.org/10.1134/s0012500809070064.
Повний текст джерелаBochkarev, Mikhail N., Anatoly A. Fagin, Nikolai O. Druzhkov, Vladimir K. Cherkasov, Marina A. Katkova, Georgy K. Fukin, and Yurii A. Kurskii. "Synthesis and characterization of phenanthren-o-iminoquinone complexes of rare earth metals." Journal of Organometallic Chemistry 695, no. 25-26 (December 2010): 2774–80. http://dx.doi.org/10.1016/j.jorganchem.2010.06.024.
Повний текст джерелаXue, Bing, Wei Wang, Jiang-Jiang Qin, Bhavitavya Nijampatnam, Srinivasan Murugesan, Veronika Kozlovskaya, Ruiwen Zhang, Sadanandan E. Velu, and Eugenia Kharlampieva. "Highly efficient delivery of potent anticancer iminoquinone derivative by multilayer hydrogel cubes." Acta Biomaterialia 58 (August 2017): 386–98. http://dx.doi.org/10.1016/j.actbio.2017.06.004.
Повний текст джерелаChegerev, Maxim G., Alexandr V. Piskunov, Alyona A. Starikova, Stanislav P. Kubrin, Georgy K. Fukin, Vladimir K. Cherkasov, and Gleb A. Abakumov. "Redox Isomerism in Main-Group Chemistry: Tin Complex with o -Iminoquinone Ligands." European Journal of Inorganic Chemistry 2018, no. 9 (March 2, 2018): 1087–92. http://dx.doi.org/10.1002/ejic.201701361.
Повний текст джерелаChagas, Manoel P., Josué C. C. Santos, Eduardo B. G. N. Santos, Tiago D. Oliveira, and Mauro Korn. "Exploiting iminoquinone free radical production for thiol based drugs determination in pharmaceutical formulations." Journal of the Brazilian Chemical Society 20, no. 9 (2009): 1646–52. http://dx.doi.org/10.1590/s0103-50532009000900012.
Повний текст джерелаSpeier, Gabor, Jozsef Csihony, Anne M. Whalen та Cortlandt G. Pierpont. "Iminoquinone coordination to copper(I) in the [Cu(PhenoxBQ)(μ-Cl)]2 dimer". Inorganica Chimica Acta 245, № 1 (квітень 1996): 1–5. http://dx.doi.org/10.1016/0020-1693(95)04792-1.
Повний текст джерелаRochford, Jonathan, Ming-Kang Tsai, David J. Szalda, Julie L. Boyer, James T. Muckerman, and Etsuko Fujita. "Oxidation State Characterization of Ruthenium 2−Iminoquinone Complexes through Experimental and Theoretical Studies." Inorganic Chemistry 49, no. 3 (February 2010): 860–69. http://dx.doi.org/10.1021/ic901194k.
Повний текст джерелаSkibo, E. B. "The Discovery of the Pyrrolo[1,2-a]benzimidazole Antitumor Agents - The Design of Selective Antitumor Agents." Current Medicinal Chemistry 3, no. 1 (February 1996): 47–78. http://dx.doi.org/10.2174/092986730301220224163834.
Повний текст джерелаSweeney, Martin, Darren Conboy, Styliana I. Mirallai, and Fawaz Aldabbagh. "Advances in the Synthesis of Ring-Fused Benzimidazoles and Imidazobenzimidazoles." Molecules 26, no. 9 (May 4, 2021): 2684. http://dx.doi.org/10.3390/molecules26092684.
Повний текст джерелаImamura, Keisuke. "Construction of Multi-Nitrogen-Containing Iminoquinone Skeleton and its Application to Natural Product Synthesis." Journal of Synthetic Organic Chemistry, Japan 64, no. 8 (2006): 867–68. http://dx.doi.org/10.5059/yukigoseikyokaishi.64.867.
Повний текст джерелаPiskunov, A. V., M. G. Chegerev, L. B. Vaganova, and G. K. Fukin. "New paramagnetic tin(IV) complexes based on o-iminoquinone ligands: Synthesis and thermal transformation." Russian Journal of Coordination Chemistry 41, no. 7 (June 24, 2015): 428–35. http://dx.doi.org/10.1134/s1070328415070076.
Повний текст джерелаFernandes, Luiza, Nathalia Moraes, Fernanda S. Sagrillo, Augusto V. Magalhães, Marcela C. de Moraes, Luciana Romão, Jeffery W. Kelly, Debora Foguel, Neil P. Grimster, and Fernando L. Palhano. "An ortho-Iminoquinone Compound Reacts with Lysine Inhibiting Aggregation while Remodeling Mature Amyloid Fibrils." ACS Chemical Neuroscience 8, no. 8 (May 4, 2017): 1704–12. http://dx.doi.org/10.1021/acschemneuro.7b00017.
Повний текст джерелаBucher, Götz. "Photochemical Generation of Iminoquinone Methides by 1,4-Hydrogen Migration in Derivatives of o-Tolylnitrene." European Journal of Organic Chemistry 2001, no. 13 (July 2001): 2447–62. http://dx.doi.org/10.1002/1099-0690(200107)2001:13<2447::aid-ejoc2447>3.0.co;2-n.
Повний текст джерелаPiskunov, Alexandr V., Arina V. Maleeva, Irina N. Mescheryakova, and Georgii K. Fukin. "The Reduction of Sterically Hindered o-Quinone and o-Iminoquinone with Gallium and “GaI”." European Journal of Inorganic Chemistry 2012, no. 27 (August 8, 2012): 4318–26. http://dx.doi.org/10.1002/ejic.201200535.
Повний текст джерелаBucher, Götz, and Hans-Gert Korth. "Photochemistry ofortho-Phenoxymethyl-Substituted Aryl Azides: A Novel Nitrene Rearrangement En Route to Isolable Iminoquinone Methides?" Angewandte Chemie International Edition 38, no. 1-2 (January 15, 1999): 212–15. http://dx.doi.org/10.1002/(sici)1521-3773(19990115)38:1/2<212::aid-anie212>3.0.co;2-9.
Повний текст джерелаWen, Bo, and David J. Moore. "Bioactivation of Glafenine by Human Liver Microsomes and Peroxidases: Identification of Electrophilic Iminoquinone Species and GSH Conjugates." Drug Metabolism and Disposition 39, no. 9 (May 31, 2011): 1511–21. http://dx.doi.org/10.1124/dmd.111.039396.
Повний текст джерелаChegerev, M. G., and A. V. Piskunov. "Chemistry of Complexes of Group 14 Elements Based on Redox-Active Ligands of the o-Iminoquinone Type." Russian Journal of Coordination Chemistry 44, no. 4 (April 2018): 258–71. http://dx.doi.org/10.1134/s1070328418040036.
Повний текст джерелаPei, Jiying, Cheng-Chih Hsu, Ruijie Zhang, Yinghui Wang, Kefu Yu, and Guangming Huang. "Unexpected Reduction of Iminoquinone and Quinone Derivatives in Positive Electrospray Ionization Mass Spectrometry and Possible Mechanism Exploration." Journal of The American Society for Mass Spectrometry 28, no. 11 (August 7, 2017): 2454–61. http://dx.doi.org/10.1007/s13361-017-1770-4.
Повний текст джерелаLazarev, Georgii G., Francisco Lara, Federico Garcia, and Anton Rieker. "Radical pairs during photolysis of an iminoquinone in single crystals of 2,6-di-tert-butyl-4-methylphenol." Chemical Physics Letters 199, no. 1-2 (October 1992): 29–32. http://dx.doi.org/10.1016/0009-2614(92)80044-c.
Повний текст джерелаHu, Ching-Yao, Yu-Jung Liu, and Wen-Hui Kuan. "pH-Dependent Degradation of Diclofenac by a Tunnel-Structured Manganese Oxide." Water 12, no. 8 (August 5, 2020): 2203. http://dx.doi.org/10.3390/w12082203.
Повний текст джерелаWhalen, Anne M., Samaresh Bhattacharya, and Cortlandt G. Pierpont. "Iminoquinone complexes of iron and nickel. Structural, magnetic, and electrochemical properties of complexes containing the phenoxazinolate semiquinone radical." Inorganic Chemistry 33, no. 2 (January 1994): 347–53. http://dx.doi.org/10.1021/ic00080a025.
Повний текст джерелаDruzhkov, N. O., I. N. Meshcheryakova, A. V. Cherkasov, and A. V. Piskunov. "New functionalized ditopic redox-active hydroxy-p-iminoquinone-type ligands and mercury(ii) complexes based on these ligands." Russian Chemical Bulletin 69, no. 1 (January 2020): 49–60. http://dx.doi.org/10.1007/s11172-020-2722-x.
Повний текст джерелаBucher, Götz. "A Laser Flash Photolysis Study on 2-Azido-N,N-diethylbenzylamine − The Reactivity of Iminoquinone Methides in Solution." European Journal of Organic Chemistry 2001, no. 13 (July 2001): 2463–75. http://dx.doi.org/10.1002/1099-0690(200107)2001:13<2463::aid-ejoc2463>3.0.co;2-6.
Повний текст джерелаChegerev, Maxim G., Alyona A. Starikova, Alexander V. Piskunov, and Vladimir K. Cherkasov. "Valence Tautomerism in Main-Group Complexes? Computational Modeling of Si, Ge, Sn, and Pb Bischelates witho-Iminoquinone Ligands." European Journal of Inorganic Chemistry 2016, no. 2 (December 7, 2015): 252–58. http://dx.doi.org/10.1002/ejic.201501155.
Повний текст джерелаSmith, Arnold L., Alice L. Erwin, Toni Kline, William C. T. Unrath, Kevin Nelson, Allan Weber, and William N. Howald. "Chloramphenicol Is a Substrate for a Novel Nitroreductase Pathway in Haemophilus influenzae." Antimicrobial Agents and Chemotherapy 51, no. 8 (August 2007): 2820–29. http://dx.doi.org/10.1128/aac.00087-07.
Повний текст джерелаIslam, Imadul, and Edward B. Skibo. "Synthesis and physical studies of azamitosene and iminoazamitosene reductive alkylating agents. Iminoquinone hydrolytic stability, syn/anti isomerization, and electrochemistry." Journal of Organic Chemistry 55, no. 10 (May 1990): 3195–205. http://dx.doi.org/10.1021/jo00297a040.
Повний текст джерелаZlotkowski, Katherine, William M. Hewitt, Pengcheng Yan, Heidi R. Bokesch, Megan L. Peach, Marc C. Nicklaus, Barry R. O’Keefe, James B. McMahon, Kirk R. Gustafson, and John S. Schneekloth. "Macrophilone A: Structure Elucidation, Total Synthesis, and Functional Evaluation of a Biologically Active Iminoquinone from the Marine HydroidMacrorhynchia philippina." Organic Letters 19, no. 7 (March 27, 2017): 1726–29. http://dx.doi.org/10.1021/acs.orglett.7b00496.
Повний текст джерелаRaju, Selvam, Pratheepkumar Annamalai, Pei-Ling Chen, Yi-Hung Liu, and Shih-Ching Chuang. "Iptycenes with an acridinone motif developed through [4+2] cycloaddition of tethered naphthalene and iminoquinone via a radical reaction." Chemical Communications 53, no. 46 (2017): 6247–50. http://dx.doi.org/10.1039/c7cc03030d.
Повний текст джерелаBucher, Goetz, and Hans-Gert Korth. "ChemInform Abstract: Photochemistry of ortho-Phenoxymethyl-Substituted Aryl Azides: A Novel Nitrene Rearrangement En Route to Isolable Iminoquinone Methides?" ChemInform 30, no. 18 (June 16, 2010): no. http://dx.doi.org/10.1002/chin.199918052.
Повний текст джерелаPierdominici-Sottile, Gustavo, Marcelo A. Martí, and Juliana Palma. "The role of residue Thr122 of methylamine dehydrogenase on the proton transfer from the iminoquinone intermediate to residue Asp76." Chemical Physics Letters 456, no. 4-6 (May 2008): 243–46. http://dx.doi.org/10.1016/j.cplett.2008.03.023.
Повний текст джерелаPiskunov, A. V., I. V. Ershova, M. V. Gulenova, K. I. Pashanova, A. S. Bogomyakov, I. V. Smolyaninov, G. K. Fukin, and V. K. Cherkasov. "Effect of an additional functional group on the structure and properties of copper(II) and nickel(II) o-iminoquinone complexes." Russian Chemical Bulletin 64, no. 3 (March 2015): 642–49. http://dx.doi.org/10.1007/s11172-015-0912-8.
Повний текст джерелаWen, Bo, and Mingyan Zhou. "Metabolic activation of the phenothiazine antipsychotics chlorpromazine and thioridazine to electrophilic iminoquinone species in human liver microsomes and recombinant P450s." Chemico-Biological Interactions 181, no. 2 (October 2009): 220–26. http://dx.doi.org/10.1016/j.cbi.2009.05.014.
Повний текст джерелаBera, Sachinath, Sandip Mondal, Suvendu Maity, Thomas Weyhermüller, and Prasanta Ghosh. "Radical and Non-Radical States of the [Os(PIQ)] Core (PIQ = 9,10-Phenanthreneiminoquinone): Iminosemiquinone to Iminoquinone Conversion Promoted o-Metalation Reaction." Inorganic Chemistry 55, no. 10 (May 5, 2016): 4746–56. http://dx.doi.org/10.1021/acs.inorgchem.6b00040.
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