Добірка наукової літератури з теми "Iminoquinone"
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Статті в журналах з теми "Iminoquinone"
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 джерелаДисертації з теми "Iminoquinone"
Ju, Changqing. "Reactive iminoquinone metabolites of indomethacin and carbamazepine, implications for drug-induced idiosyncratic reactions." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape9/PQDD_0007/NQ41183.pdf.
Повний текст джерелаLai, Weidong George. "Bioactivation of trimethoprim, fluperlapine and nevirapine, roles of iminoquinone-type Michael acceptors in idiosyncratic drug reactions." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp03/NQ49973.pdf.
Повний текст джерелаDas, Hari Sankar [Verfasser], and Biprajit [Akademischer Betreuer] Sarkar. "Ruthenium complexes with non-innocent quinonoid, quinoline-5,8-dione and iminoquinone ligands : synthesis, structure, redox properties and electron distribution / Hari Sankar Das. Betreuer: Biprajit Sarkar." Stuttgart : Universitätsbibliothek der Universität Stuttgart, 2012. http://d-nb.info/102604331X/34.
Повний текст джерела(6629939), Ezra J. Coughlin. "Facilitating Multi-Electron Chemistry in the F-Block Using Iminoquinone Ligands." Thesis, 2019.
Знайти повний текст джерелаThe chemistry of the f-block is relatively unknown when compared to the rest of the periodic table. Transition metals and main group elements have enjoyed thorough study and development over the last 200 years, while many of the lanthanides and actinides weren’t even discovered until the 1940’s. This is troublesome, as knowledge of these elements is critical for environmental, industrial and technological advances. Understanding bonding motifs and reactivity pathways is fundamental to advancing the field of f-block chemistry. The use of redox- active ligands has aided in the construction of new bonding modes and discovery of new reaction pathways by providing electrons for these transformations. A particularly successful partnership is formed when redox-active ligands are combined with lanthanides, as these elements are usually considered redox-restricted. A series of lanthanide complexes featuring the iminoquinone ligand in three oxidation states will be discussed. The use of the ligands as a source of electrons for reactivity is also described, with new bonding motifs for lanthanides being realized. The iminoquinone ligand can also serve to break bonds. The uranyl (UO22+) ion is notoriously difficult to handle due to its strong U-O multiple bonds. To overcome this, we developed a series of uranyl complexes and studied the ability of the iminoquinone ligand to serve as an electron source for reduction of uranium, with concomitant U-O bond cleavage.
Книги з теми "Iminoquinone"
Ju, Changqing. Reactive iminoquinone metabolites of indomethacin and carbamazepine: Implications for drug-induced idiosyncratic reactions. 1999.
Знайти повний текст джерелаLai, Weidong George. Bioactivation of trimethoprim, fluperlapine and nevirapine: roles of iminoquinine-type michael acceptors in idiosyncratic drug reactions. 2000.
Знайти повний текст джерелаЧастини книг з теми "Iminoquinone"
Marcotte, Ian, Jean Marc Chapuzet, Yves Dory, and Jean Lessard. "Iminoquinones as Electrogenerated Electrophilic Species." In Novel Trends in Electroorganic Synthesis, 65–68. Tokyo: Springer Japan, 1998. http://dx.doi.org/10.1007/978-4-431-65924-2_18.
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