Статті в журналах з теми "Oxygenation Reactions"
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Das, Ujjwal. "Platinum Group Metals Bonded Thiolato Sulfur Oxygenation: Photoactivity and Bioactivity." Asian Journal of Chemistry 34, no. 12 (2022): 3059–70. http://dx.doi.org/10.14233/ajchem.2022.24007.
Повний текст джерелаForchetta, Mattia, Francesca Valentini, Valeria Conte, Pierluca Galloni, and Federica Sabuzi. "Photocatalyzed Oxygenation Reactions with Organic Dyes: State of the Art and Future Perspectives." Catalysts 13, no. 2 (January 18, 2023): 220. http://dx.doi.org/10.3390/catal13020220.
Повний текст джерелаBopp, Charlotte E., Hans-Peter E. Kohler, and Thomas B. Hofstetter. "Enzyme Kinetics of Organic Contaminant Oxygenations." CHIMIA International Journal for Chemistry 74, no. 3 (March 25, 2020): 108–14. http://dx.doi.org/10.2533/chimia.2020.108.
Повний текст джерелаYu, Mohan, and Yajun Liu. "A QM/MM Study on the Initiation Reaction of Firefly Bioluminescence—Enzymatic Oxidation of Luciferin." Molecules 26, no. 14 (July 12, 2021): 4222. http://dx.doi.org/10.3390/molecules26144222.
Повний текст джерелаTang, Conghui, Xu Qiu, Zengrui Cheng, and Ning Jiao. "Molecular oxygen-mediated oxygenation reactions involving radicals." Chemical Society Reviews 50, no. 14 (2021): 8067–101. http://dx.doi.org/10.1039/d1cs00242b.
Повний текст джерелаCheng, Xiaokai, Xingen Hu, and Zhan Lu. "Visible-Light-Promoted Aerobic Homogenous Oxygenation Reactions." Chinese Journal of Organic Chemistry 37, no. 2 (2017): 251. http://dx.doi.org/10.6023/cjoc201609022.
Повний текст джерелаFukuzumi, Shunichi, Yong‐Min Lee, and Wonwoo Nam. "Photocatalytic Oxygenation Reactions Using Water and Dioxygen." ChemSusChem 12, no. 17 (July 25, 2019): 3931–40. http://dx.doi.org/10.1002/cssc.201901276.
Повний текст джерелаPerez, Daniel I., Maria Mifsud Grau, Isabel W. C. E. Arends, and Frank Hollmann. "Visible light-driven and chloroperoxidase-catalyzed oxygenation reactions." Chemical Communications, no. 44 (2009): 6848. http://dx.doi.org/10.1039/b915078a.
Повний текст джерелаMihara, Satoru, and Hideki Tateba. "Photosensitized oxygenation reactions of phytol and its derivatives." Journal of Organic Chemistry 51, no. 7 (April 1986): 1142–44. http://dx.doi.org/10.1021/jo00357a043.
Повний текст джерелаMONTANARI, F., S. BANFI, G. POZZI, and S. QUICI. "ChemInform Abstract: Oxygenation Reactions under Two-Phase Conditions." ChemInform 26, no. 20 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199520261.
Повний текст джерелаBian, Changliang, Atul K. Singh, Linbin Niu, Hong Yi, and Aiwen Lei. "Visible‐Light‐Mediated Oxygenation Reactions using Molecular Oxygen." Asian Journal of Organic Chemistry 6, no. 4 (February 27, 2017): 386–96. http://dx.doi.org/10.1002/ajoc.201600563.
Повний текст джерелаŠagud, Ivana, and Irena Škorić. "Photocatalytic Oxygenation by Water-Soluble Metalloporphyrins as a Pathway to Functionalized Polycycles." International Journal of Photoenergy 2018 (December 30, 2018): 1–8. http://dx.doi.org/10.1155/2018/1017957.
Повний текст джерелаTAKAGUCHI, YUTAKA, TAKAAKI TSUBOI, YUUKI SAKO, and SADAO TSUBOI. "SYNTHESIS OF FULLERODENDRON AND ITS PHOTOCATALITIC ACTIVITY." International Journal of Nanoscience 05, no. 04n05 (August 2006): 593–97. http://dx.doi.org/10.1142/s0219581x0600484x.
Повний текст джерелаМальцева and L. Maltseva. "Hyperoxia effect on humoral and cell components of immunobiological resistance of healthy rats in experiment." Journal of New Medical Technologies. eJournal 8, no. 1 (November 5, 2014): 1–6. http://dx.doi.org/10.12737/4112.
Повний текст джерелаMlakić, Milena, Anita Šalić, Matea Bačić, Bruno Zelić, Ivana Šagud, Ottó Horváth, and Irena Škorić. "Photocatalytic Oxygenation of Heterostilbenes—Batch versus Microflow Reactor." Catalysts 11, no. 3 (March 20, 2021): 395. http://dx.doi.org/10.3390/catal11030395.
Повний текст джерелаVuk, Dragana, Ottó Horváth, and Irena Škorić. "New Functionalized Polycycles Obtained by Photocatalytic Oxygenation Using Mn(III) Porphyrins in Basic Media." Catalysts 9, no. 4 (March 27, 2019): 304. http://dx.doi.org/10.3390/catal9040304.
Повний текст джерелаPaul, Melanie, Alexander Hoffmann, and Sonja Herres-Pawlis. "Room temperature stable multitalent: highly reactive and versatile copper guanidine complexes in oxygenation reactions." JBIC Journal of Biological Inorganic Chemistry 26, no. 2-3 (February 17, 2021): 249–63. http://dx.doi.org/10.1007/s00775-021-01849-9.
Повний текст джерелаLiang, Yujie, Shi-Hui Shi, Rui Jin, Xu Qiu, Jialiang Wei, Hui Tan, Xue Jiang, Xiaomeng Shi, Song Song, and Ning Jiao. "Electrochemically induced nickel catalysis for oxygenation reactions with water." Nature Catalysis 4, no. 2 (January 11, 2021): 116–23. http://dx.doi.org/10.1038/s41929-020-00559-w.
Повний текст джерелаKalyani, Dipannita, and Melanie S. Sanford. "Regioselectivity in Palladium-Catalyzed C−H Activation/Oxygenation Reactions." Organic Letters 7, no. 19 (September 2005): 4149–52. http://dx.doi.org/10.1021/ol051486x.
Повний текст джерелаLimberg, Christian. "The Role of Radicals in Metal-Assisted Oxygenation Reactions." Angewandte Chemie International Edition 42, no. 48 (December 15, 2003): 5932–54. http://dx.doi.org/10.1002/anie.200300578.
Повний текст джерелаMEUNIER, B., and S. CAMPESTRINI. "ChemInform Abstract: Oxygenation Reactions Catalyzed by Supported Sulfonated Metalloporphyrins." ChemInform 24, no. 46 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199346305.
Повний текст джерелаBenders, Stefan, Florian Strassl, Bastian Fenger, Bernhard Blümich, Sonja Herres-Pawlis, and Markus Küppers. "Imaging of copper oxygenation reactions in a bubble flow." Magnetic Resonance in Chemistry 56, no. 9 (May 17, 2018): 826–30. http://dx.doi.org/10.1002/mrc.4742.
Повний текст джерелаKonrad, David, Bilal Kicin, and Dirk Trauner. "Concise Asymmetric Synthesis of Kweichowenol A." Synlett 30, no. 04 (December 17, 2018): 383–86. http://dx.doi.org/10.1055/s-0037-1610390.
Повний текст джерелаYang, Chun-Hua, Wen-Wen Fan, Gong-Qing Liu, Lili Duan, Lin Li, and Yue-Ming Li. "On the understanding of BF3·Et2O-promoted intra- and intermolecular amination and oxygenation of unfunctionalized olefins." RSC Advances 5, no. 75 (2015): 61081–93. http://dx.doi.org/10.1039/c5ra10513g.
Повний текст джерелаLindhorst, A. C., S. Haslinger, and Fritz E. Kühn. "Molecular iron complexes as catalysts for selective C–H bond oxygenation reactions." Chemical Communications 51, no. 97 (2015): 17193–212. http://dx.doi.org/10.1039/c5cc07146a.
Повний текст джерелаSchendera, Eva, Alexander Villinger, and Malte Brasholz. "Photoinduced iodine-mediated tandem dehydrogenative Povarov cyclisation/C–H oxygenation reactions." Organic & Biomolecular Chemistry 18, no. 35 (2020): 6912–15. http://dx.doi.org/10.1039/d0ob01494j.
Повний текст джерелаFukuzumi, Shunichi, Yong-Min Lee, and Wonwoo Nam. "Photocatalytic redox reactions with metalloporphyrins." Journal of Porphyrins and Phthalocyanines 24, no. 01n03 (January 2020): 21–32. http://dx.doi.org/10.1142/s1088424619300131.
Повний текст джерелаYang, Lili, Fang Wang, Jiali Gao, and Yong Wang. "What factors tune the chemical equilibrium between metal-iodosylarene oxidants and high-valent metal-oxo ones?" Physical Chemistry Chemical Physics 21, no. 3 (2019): 1271–76. http://dx.doi.org/10.1039/c8cp06117c.
Повний текст джерелаSzakács, Zoltán, Mihály Kállay, and Miklós Kubinyi. "Theoretical study on the photooxygenation and photorearrangement reactions of 3-hydroxyflavone." RSC Advances 7, no. 51 (2017): 32185–92. http://dx.doi.org/10.1039/c7ra04590e.
Повний текст джерелаNehru, Kasi, Soo Jeong Kim, In Young Kim, Mi Sook Seo, Youngmee Kim, Sung-Jin Kim, Jinheung Kim, and Wonwoo Nam. "A highly efficient non-heme manganese complex in oxygenation reactions." Chemical Communications, no. 44 (2007): 4623. http://dx.doi.org/10.1039/b708976g.
Повний текст джерелаBonaventura, Celia, Robert Henkens, Abdu I. Alayash, Sambuddha Banerjee, and Alvin L. Crumbliss. "Molecular Controls of the Oxygenation and Redox Reactions of Hemoglobin." Antioxidants & Redox Signaling 18, no. 17 (June 10, 2013): 2298–313. http://dx.doi.org/10.1089/ars.2012.4947.
Повний текст джерелаHetterscheid, Dennis G. H., and Bas de Bruin. "Open-shell rhodium and iridium species in (catalytic) oxygenation reactions." Journal of Molecular Catalysis A: Chemical 251, no. 1-2 (May 2006): 291–96. http://dx.doi.org/10.1016/j.molcata.2006.02.009.
Повний текст джерелаGollnick, Klaus, and Stephan Held. "Hydroxyanthraquinones as sensitizers of electron-transfer-induced photo-oxygenation reactions." Journal of Photochemistry and Photobiology A: Chemistry 70, no. 2 (February 1993): 135–45. http://dx.doi.org/10.1016/1010-6030(93)85033-5.
Повний текст джерелаYoon, Jihae, Samuel A Wilson, Yu Kyeong Jang, Mi Sook Seo, Kasi Nehru, Britt Hedman, Keith O Hodgson, Eckhard Bill, Edward I Solomon, and Wonwoo Nam. "Reactive Intermediates in Oxygenation Reactions with Mononuclear Nonheme Iron Catalysts." Angewandte Chemie International Edition 48, no. 7 (January 9, 2009): 1257–60. http://dx.doi.org/10.1002/anie.200802672.
Повний текст джерелаYoon, Jihae, Samuel A Wilson, Yu Kyeong Jang, Mi Sook Seo, Kasi Nehru, Britt Hedman, Keith O Hodgson, Eckhard Bill, Edward I Solomon, and Wonwoo Nam. "Reactive Intermediates in Oxygenation Reactions with Mononuclear Nonheme Iron Catalysts." Angewandte Chemie 121, no. 7 (January 9, 2009): 1283–86. http://dx.doi.org/10.1002/ange.200802672.
Повний текст джерелаJiang, Yi-Fan, Cheng-Zong Yuan, Xiao Zhou, Hong-Li Guo, Ya-Nan Liu, Nan Jiang, and An-Wu Xu. "Highly efficient redox-driven reversible color switching of dye molecules via hydrogenation/oxygenation." Chemical Communications 53, no. 2 (2017): 360–63. http://dx.doi.org/10.1039/c6cc08500h.
Повний текст джерелаLiu, Ya-Nan, Xiao Zhou, Xin Wang, Kuang Liang, Zheng-Kun Yang, Cong-Cong Shen, M. Imran, Shafaq Sahar, and An-Wu Xu. "Hydrogenation/oxidation induced efficient reversible color switching between methylene blue and leuco-methylene blue." RSC Advances 7, no. 48 (2017): 30080–85. http://dx.doi.org/10.1039/c7ra04498d.
Повний текст джерелаLi, Ze-lin, Kang-kang Sun, and Chun Cai. "Nickel-catalyzed regioselective C–H oxygenation: new routes for versatile C–O bond formation." Organic Chemistry Frontiers 6, no. 5 (2019): 637–42. http://dx.doi.org/10.1039/c8qo01274a.
Повний текст джерелаFerraro, Daniel J., Adam Okerlund, Eric Brown, and S. Ramaswamy. "One enzyme, many reactions: structural basis for the various reactions catalyzed by naphthalene 1,2-dioxygenase." IUCrJ 4, no. 5 (August 8, 2017): 648–56. http://dx.doi.org/10.1107/s2052252517008223.
Повний текст джерелаFukuzumi, Shunichi. "Electron transfer and catalysis with high-valent metal-oxo complexes." Dalton Transactions 44, no. 15 (2015): 6696–705. http://dx.doi.org/10.1039/c5dt00204d.
Повний текст джерелаSaleem-Batcha, Raspudin, Frederick Stull, Jacob N. Sanders, Bradley S. Moore, Bruce A. Palfey, K. N. Houk, and Robin Teufel. "Enzymatic control of dioxygen binding and functionalization of the flavin cofactor." Proceedings of the National Academy of Sciences 115, no. 19 (April 23, 2018): 4909–14. http://dx.doi.org/10.1073/pnas.1801189115.
Повний текст джерелаZhou, Xin-Yan, Bo Fu, Wen-Dong Jin, Xiong Wang, Ke-Ke Wang, Mei Wang, Yuan-Bin She, and Hai-Min Shen. "Efficient and Selective Oxygenation of Cycloalkanes and Alkyl Aromatics with Oxygen through Synergistic Catalysis of Bimetallic Active Centers in Two-Dimensional Metal-Organic Frameworks Based on Metalloporphyrins." Biomimetics 8, no. 3 (July 21, 2023): 325. http://dx.doi.org/10.3390/biomimetics8030325.
Повний текст джерелаYang, Hsuan, Chia-Pei Chung, Ying-Chih Lin, and Yi-Hong Liu. "Facile oxygenation reactions of ruthenium acetylide complex containing substituted olefinic group." Dalton Transactions 40, no. 14 (2011): 3703. http://dx.doi.org/10.1039/c0dt01551b.
Повний текст джерелаBremner, David H., and Neil S. Ringan. "Chemistry of cephems: C-4 substitution and sulphoxide de-oxygenation reactions." Journal of the Chemical Society, Perkin Transactions 1, no. 5 (1991): 1265. http://dx.doi.org/10.1039/p19910001265.
Повний текст джерелаMatsui, Toshitaka, Masaki Unno, and Masao Ikeda-Saito. "Heme Oxygenase Reveals Its Strategy for Catalyzing Three Successive Oxygenation Reactions." Accounts of Chemical Research 43, no. 2 (February 16, 2010): 240–47. http://dx.doi.org/10.1021/ar9001685.
Повний текст джерелаFukuzumi, Shunichi, Takashi Kishi, Hiroaki Kotani, Yong-Min Lee, and Wonwoo Nam. "Highly efficient photocatalytic oxygenation reactions using water as an oxygen source." Nature Chemistry 3, no. 1 (November 28, 2010): 38–41. http://dx.doi.org/10.1038/nchem.905.
Повний текст джерелаYuan, Zhiwen, and Jeanne M. VanBriesen. "Yield prediction and stoichiometry of multi-step biodegradation reactions involving oxygenation." Biotechnology and Bioengineering 80, no. 1 (August 15, 2002): 100–113. http://dx.doi.org/10.1002/bit.10355.
Повний текст джерелаAkaba, Ryoichi, Masaki Kamata, Akiko Koike, Ken-Ichi Mogi, Yasunao Kuriyama, and Hirochika Sakuragi. "Thiapyrylium salt-sensitized electron transfer reactions oftrans-stilbene. Dimerization and oxygenation." Journal of Physical Organic Chemistry 10, no. 11 (November 1997): 861–69. http://dx.doi.org/10.1002/(sici)1099-1395(199711)10:11<861::aid-pca947>3.0.co;2-l.
Повний текст джерелаKHAN, M. M. T. "ChemInform Abstract: Oxidation and Oxygenation Reactions Catalyzed by Ruthenium(III) Complexes." ChemInform 23, no. 50 (September 1, 2010): no. http://dx.doi.org/10.1002/chin.199250302.
Повний текст джерелаBalestra, Costantino, and Jacek Kot. "Oxygen: A Stimulus, Not “Only” a Drug." Medicina 57, no. 11 (October 25, 2021): 1161. http://dx.doi.org/10.3390/medicina57111161.
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