Статті в журналах з теми "Hydroxylation reactions"
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Holland, Herbert L., Frances M. Brown, P. Chinna Chenchaiah, and J. Appa Rao. "Hydroxylation of prostanoids by fungi. Synthesis of (−)-15-deoxy-19-(R)-hydroxy-PGE1 and (−)-15-deoxy-18-(S)-hydroxy-PGE1." Canadian Journal of Chemistry 68, no. 2 (February 1, 1990): 282–93. http://dx.doi.org/10.1139/v90-039.
Повний текст джерелаHolland, Herbert L., and Hedda K. Weber. "Enzymatic hydroxylation reactions." Current Opinion in Biotechnology 11, no. 6 (December 2000): 547–53. http://dx.doi.org/10.1016/s0958-1669(00)00142-7.
Повний текст джерелаZimniak, P., E. J. Holsztynska, A. Radominska, M. Iscan, R. Lester та D. J. Waxman. "Distinct forms of cytochrome P-450 are responsible for 6β-hydroxylation of bile acids and of neutral steroids". Biochemical Journal 275, № 1 (1 квітня 1991): 105–11. http://dx.doi.org/10.1042/bj2750105.
Повний текст джерелаFan, Tengjiao, Guohui Sun, Lijiao Zhao, Xin Cui, and Rugang Zhong. "Metabolic Activation and Carcinogenesis of Tobacco-Specific Nitrosamine N’-Nitrosonornicotine (NNN): A Density Function Theory and Molecular Docking Study." International Journal of Environmental Research and Public Health 16, no. 2 (January 9, 2019): 178. http://dx.doi.org/10.3390/ijerph16020178.
Повний текст джерелаHolland, Herbert L. "ChemInform Abstract: Stereoselective Hydroxylation Reactions." ChemInform 32, no. 21 (May 26, 2010): no. http://dx.doi.org/10.1002/chin.200121255.
Повний текст джерелаDardonville, Christophe, Henri Virelizier, Jean Boivin, and Christopher K. Jankowski. "Reactions of carboline." Spectroscopy 13, no. 4 (1997): 257–64. http://dx.doi.org/10.1155/1997/821241.
Повний текст джерелаCryle, Max J., Jeanette E. Stok, and James J. De Voss. "Reactions Catalyzed by Bacterial Cytochromes P450." Australian Journal of Chemistry 56, no. 8 (2003): 749. http://dx.doi.org/10.1071/ch03040.
Повний текст джерелаAgarwal, Mahadev, Neelam Singla, and S. K. Singh. "To Synthesis and Characterization of Novel 1,3,4-Oxadiazinoindole Derivatives for the Purpose of Antidepressant Activity." INTERNATIONAL JOURNAL OF PHARMACEUTICAL QUALITY ASSURANCE 14, no. 03 (September 25, 2023): 656–60. http://dx.doi.org/10.25258/ijpqa.14.3.33.
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 джерелаCadot, Christine, Peter I. Dalko, Janine Cossy, Cyril Ollivier, Rachel Chuard, and Philippe Renaud. "Free-Radical Hydroxylation Reactions of Alkylboronates." Journal of Organic Chemistry 67, no. 21 (October 2002): 7193–202. http://dx.doi.org/10.1021/jo0201833.
Повний текст джерелаLee, Gun Dae, Sung Gab Kim, Hee Hoon Jeong, Seong Soo Park, and Seong Soo Hong. "Photocatalytic Hydroxylation of Phenol over Ti-Containing Zeolites (TS-1, Ti-MCM-41)." Solid State Phenomena 124-126 (June 2007): 1793–96. http://dx.doi.org/10.4028/www.scientific.net/ssp.124-126.1793.
Повний текст джерелаFlashman, Emily, Sarah L. Davies, Kar Kheng Yeoh, and Christopher J. Schofield. "Investigating the dependence of the hypoxia-inducible factor hydroxylases (factor inhibiting HIF and prolyl hydroxylase domain 2) on ascorbate and other reducing agents." Biochemical Journal 427, no. 1 (March 15, 2010): 135–42. http://dx.doi.org/10.1042/bj20091609.
Повний текст джерелаMorrone, Dana, Xiaoming Chen, Robert M. Coates, and Reuben J. Peters. "Characterization of the kaurene oxidase CYP701A3, a multifunctional cytochrome P450 from gibberellin biosynthesis." Biochemical Journal 431, no. 3 (October 11, 2010): 337–47. http://dx.doi.org/10.1042/bj20100597.
Повний текст джерелаSingh, Kuldeep, Kulbir Kulbir, Tarang Gupta, Rajneesh Kaur, and Raman Singh. "Applications of Rozen’s Reagent in Oxygen-Transfer and C–H Activation Reactions." Synthesis 51, no. 02 (November 22, 2018): 371–83. http://dx.doi.org/10.1055/s-0037-1609638.
Повний текст джерелаLee, Kyoung. "p-Hydroxylation reactions catalyzed by naphthalene dioxygenase." FEMS Microbiology Letters 255, no. 2 (February 2006): 316–20. http://dx.doi.org/10.1111/j.1574-6968.2005.00079.x.
Повний текст джерелаIanelli, S., M. Nardelli, D. Belletti, B. Jamart-Grégoire, S. Mercier-Girardot, and P. Caubère. "Stereochemistry of Hydroxylation Reactions on Polycyclic Pyrans." Acta Crystallographica Section C Crystal Structure Communications 51, no. 9 (September 15, 1995): 1885–89. http://dx.doi.org/10.1107/s0108270195001442.
Повний текст джерелаKoziol, A. E., Ruth C. Palenik, Gus J. Palenik, and Dennis W. Wester. "Structural studies of copper catalyzed hydroxylation reactions." Inorganica Chimica Acta 359, no. 8 (May 2006): 2569–74. http://dx.doi.org/10.1016/j.ica.2006.01.042.
Повний текст джерелаWong, Siew Hoon, Stephen G. Bell, and James J. De Voss. "P450 catalysed dehydrogenation." Pure and Applied Chemistry 89, no. 6 (June 27, 2017): 841–52. http://dx.doi.org/10.1515/pac-2016-1216.
Повний текст джерелаSkibiński, Robert, Jakub Trawiński, and Maciej Gawlik. "Characterization of Phase I Hepatic Metabolites of Anti-Premature Ejaculation Drug Dapoxetine by UHPLC-ESI-Q-TOF." Molecules 26, no. 13 (June 22, 2021): 3794. http://dx.doi.org/10.3390/molecules26133794.
Повний текст джерелаMunir, Widad A., and J. Barrett. "The metabolism of xenobiotic compounds by Hymenolepis diminuta (Cestoda: Cyclophyllidea)." Parasitology 91, no. 1 (August 1985): 145–56. http://dx.doi.org/10.1017/s0031182000056584.
Повний текст джерелаCrosby, Samantha V., Izzeldin Y. Ahmed, Laura R. Osborn, Zeyuan Wang, Mary A. Schleiff, William E. Fantegrossi, Swati Nagar, Paul L. Prather, Gunnar Boysen, and Grover P. Miller. "Similar 5F-APINACA Metabolism between CD-1 Mouse and Human Liver Microsomes Involves Different P450 Cytochromes." Metabolites 12, no. 8 (August 22, 2022): 773. http://dx.doi.org/10.3390/metabo12080773.
Повний текст джерелаLiu, Yi, Puying Luo, Yang Fu, Tianxin Hao, Xuan Liu, Qiuping Ding, and Yiyuan Peng. "Recent advances in the tandem annulation of 1,3-enynes to functionalized pyridine and pyrrole derivatives." Beilstein Journal of Organic Chemistry 17 (September 22, 2021): 2462–76. http://dx.doi.org/10.3762/bjoc.17.163.
Повний текст джерелаAmor, Ilef Limem-Ben, Nidhal Salem, Emmanuel Guedon, Jean-Marc Engasser, Leila Chekir-Ghedrira, and Mohamed Ghoul. "Preliminary Investigation of Naringenin Hydroxylation with Recombinant E. coli Expressing Plant Flavonoid Hydroxylation Gene." Natural Product Communications 5, no. 5 (May 2010): 1934578X1000500. http://dx.doi.org/10.1177/1934578x1000500520.
Повний текст джерелаCox, Robin A., Kap-Soo Cheon, Sam-Rok Keum, and Erwin Buncel. "Mechanism of the benzidine disproportionation of (arylhydrazo)pyridines. The reactions of 4-(4-chlorophenylazo)pyridine and -hydrazo)pyridine in acid media." Canadian Journal of Chemistry 76, no. 6 (June 1, 1998): 896–906. http://dx.doi.org/10.1139/v98-082.
Повний текст джерелаFunhoff, Enrico G., Jenny Salzmann, Ulrich Bauer, Bernard Witholt, and Jan B. van Beilen. "Hydroxylation and epoxidation reactions catalyzed by CYP153 enzymes." Enzyme and Microbial Technology 40, no. 4 (March 2007): 806–12. http://dx.doi.org/10.1016/j.enzmictec.2006.06.014.
Повний текст джерелаFan, Boyi, Baocheng Jiang, Sensen Yan, Bohui Xu, Huilian Huang та Guangtong Chen. "Anti-Inflammatory 18β-Glycyrrhetinin Acid Derivatives Produced by Biocatalysis". Planta Medica 85, № 01 (7 серпня 2018): 56–61. http://dx.doi.org/10.1055/a-0662-0296.
Повний текст джерелаAmor, Ilef Limem-Ben, Alain Hehn, Emmanuel Guedon, Kamel Ghedira, Jean-Marc Engasser, Leila Chekir-Ghedrira, and Mohamed Ghoul. "Biotransformation of Naringenin to Eriodictyol by Saccharomyces cerevisiea Functionally Expressing Flavonoid 3′ Hydroxylase." Natural Product Communications 5, no. 12 (December 2010): 1934578X1000501. http://dx.doi.org/10.1177/1934578x1000501211.
Повний текст джерелаŁyczko, Paulina, Anna Panek, and Alina Świzdor. "Highly Regioselective and Stereoselective Biohydroxylations of Oxandrolone." Catalysts 11, no. 1 (December 25, 2020): 16. http://dx.doi.org/10.3390/catal11010016.
Повний текст джерелаZHOU, YAN, KAI HU, JUNFENG SHEN, ZHENPING JI, and GONGZHEN CHENG. "ROLE OF SOLVENT IN SLURRY PHASE REACTIONS." Surface Review and Letters 15, no. 06 (December 2008): 805–8. http://dx.doi.org/10.1142/s0218625x08012190.
Повний текст джерелаIsobe, Hiroshi, Satomichi Nishihara, Mitsuo Shoji, Shusuke Yamanaka, Jiro Shimada, Masayuki Hagiwara, and Kizashi Yamaguchi. "Extended Hartree-Fock theory of chemical reactions. VIII. Hydroxylation reactions by P450." International Journal of Quantum Chemistry 108, no. 15 (2008): 2991–3009. http://dx.doi.org/10.1002/qua.21874.
Повний текст джерелаJing, Xiao-Ran, Huan Liu, Yao Nie, and Yan Xu. "2-Ketoglutarate-Generated In Vitro Enzymatic Biosystem Facilitates Fe(II)/2-Ketoglutarate-Dependent Dioxygenase-Mediated C–H Bond Oxidation for (2s,3r,4s)-4-Hydroxyisoleucine Synthesis." International Journal of Molecular Sciences 21, no. 15 (July 28, 2020): 5347. http://dx.doi.org/10.3390/ijms21155347.
Повний текст джерелаWei, Danlei, Lianqi Huang, Hanying Liang, Junhua Zou, Wenwen Chen, Can Yang, Yidong Hou, Dandan Zheng, and Jinshui Zhang. "Photocatalytic hydroxylation of benzene to phenol over organosilane-functionalized FeVO4 nanorods." Catalysis Science & Technology 11, no. 17 (2021): 5931–37. http://dx.doi.org/10.1039/d1cy00890k.
Повний текст джерелаChandra, Bittu, Kundan K. Singh, and Sayam Sen Gupta. "Selective photocatalytic hydroxylation and epoxidation reactions by an iron complex using water as the oxygen source." Chem. Sci. 8, no. 11 (2017): 7545–51. http://dx.doi.org/10.1039/c7sc02780j.
Повний текст джерелаSuzuki, Kazuto, Joshua Kyle Stanfield, Osami Shoji, Sota Yanagisawa, Hiroshi Sugimoto, Yoshitsugu Shiro, and Yoshihito Watanabe. "Control of stereoselectivity of benzylic hydroxylation catalysed by wild-type cytochrome P450BM3 using decoy molecules." Catalysis Science & Technology 7, no. 15 (2017): 3332–38. http://dx.doi.org/10.1039/c7cy01130j.
Повний текст джерелаChen, Xuwen, Wenyan Hao, and Yunyun Liu. "Copper-catalyzed tandem aryl–halogen hydroxylation and CH2Cl2-based N,O-acetalization toward the synthesis of 2,3-dihydrobenzoxazinones." Organic & Biomolecular Chemistry 15, no. 16 (2017): 3423–26. http://dx.doi.org/10.1039/c7ob00625j.
Повний текст джерелаSAFARI, NASSER, FARZAD BAHADORAN, MOHAMMAD REZA HOSEINZADEH, and REZA GHIASI. "Cytochrome P-450 model reaction: effects of substitution on the rate of aromatic hydroxylation." Journal of Porphyrins and Phthalocyanines 04, no. 03 (April 2000): 285–91. http://dx.doi.org/10.1002/(sici)1099-1409(200004/05)4:3<285::aid-jpp215>3.0.co;2-r.
Повний текст джерелаJóźwik, Ilona K., Martin Litzenburger, Yogan Khatri, Alexander Schifrin, Marco Girhard, Vlada Urlacher, Andy-Mark W. H. Thunnissen, and Rita Bernhardt. "Structural insights into oxidation of medium-chain fatty acids and flavanone by myxobacterial cytochrome P450 CYP267B1." Biochemical Journal 475, no. 17 (September 11, 2018): 2801–17. http://dx.doi.org/10.1042/bcj20180402.
Повний текст джерелаUehara, Shotaro, Toru Oshio, Kazuyuki Nakanishi, Etsuko Tomioka, Miyu Suzuki, Takashi Inoue, Yasuhiro Uno, Erika Sasaki, and Hiroshi Yamazaki. "Survey of Drug Oxidation Activities in Hepatic and Intestinal Microsomes of Individual Common Marmosets, a New Nonhuman Primate Animal Model." Current Drug Metabolism 20, no. 2 (April 30, 2019): 103–13. http://dx.doi.org/10.2174/1389200219666181003143312.
Повний текст джерелаGrüber, R., J. Aranda, A. Bellili, I. Tuñón, and E. Dumont. "Free energy profiles for two ubiquitous damaging agents: methylation and hydroxylation of guanine in B-DNA." Physical Chemistry Chemical Physics 19, no. 22 (2017): 14695–701. http://dx.doi.org/10.1039/c6cp07966k.
Повний текст джерелаOHKAWA, HIDEO, YOSHIYASU YABUSAKI, TOSHIYUKI SAKAKI, HIROKO MURAKAMI, and MEGUMI SHIBATA. "Hydroxylation Reactions by Recombinant Yeast Cells Expressing P450 Monooxygenases." Annals of the New York Academy of Sciences 613, no. 1 Enzyme Engine (December 1990): 37–43. http://dx.doi.org/10.1111/j.1749-6632.1990.tb18146.x.
Повний текст джерелаToy, Patrick H., Martin Newcomb, and Lowell P. Hager. "Hypersensitive Radical Probe Studies of Chloroperoxidase-Catalyzed Hydroxylation Reactions." Chemical Research in Toxicology 11, no. 7 (July 1998): 816–23. http://dx.doi.org/10.1021/tx9800295.
Повний текст джерелаIANELLI, S., M. NARDELLI, D. BELLETTI, B. JAMART-GREGOIRE, S. MERCIER-GIRARDOT, and P. CAUBERE. "ChemInform Abstract: Stereochemistry of Hydroxylation Reactions on Polycyclic Pyrans." ChemInform 27, no. 4 (August 12, 2010): no. http://dx.doi.org/10.1002/chin.199604041.
Повний текст джерелаAnito, Dejene Assefa, Tian-Xiong Wang, Hai-Peng Liang, Xuesong Ding, and Bao-Hang Han. "Bis(terpyridine) Ru(iii) complex functionalized porous polycarbazole for visible-light driven chemical reactions." Polymer Chemistry 12, no. 31 (2021): 4557–64. http://dx.doi.org/10.1039/d1py00527h.
Повний текст джерелаLe, Thien-Kim, Jong Hyun Park, Da Som Choi, Ga-Young Lee, Woo Sung Choi, Ki Jun Jeong, Chan Beum Park, and Chul-Ho Yun. "Solar-driven biocatalytic C-hydroxylation through direct transfer of photoinduced electrons." Green Chemistry 21, no. 3 (2019): 515–25. http://dx.doi.org/10.1039/c8gc02398k.
Повний текст джерелаEl-Sayed, Ashraf S. A., Hanaa Salah Maamoun, Gamal H. Rabie, Ibrahim Shaker, Bothaina A. Alaidaroos, Mostafa G. Ali, and Amgad M. Rady. "Microbial Tyrosinase: Biochemical, Molecular Properties and Pharmaceutical Applications." Biomedical and Pharmacology Journal 14, no. 3 (September 30, 2021): 1281–95. http://dx.doi.org/10.13005/bpj/2229.
Повний текст джерелаHolland, Herbert L., Michael J. Chernishenko, Morgan Conn, Anthony Munoz, T. Samuel Manoharan, and Michael A. Zawadski. "Enzymic hydroxylation and sulfoxidation of cyclopropyl compounds by fungal biotransformation." Canadian Journal of Chemistry 68, no. 5 (May 1, 1990): 696–700. http://dx.doi.org/10.1139/v90-107.
Повний текст джерелаAtia, Alaa A., and Masanari Kimura. "Oxidative Hydroxylation of Aryl Boronic Acid Catalyzed by Co-porphyrin Complexes via Blue-Light Irradiation." Catalysts 10, no. 11 (October 30, 2020): 1262. http://dx.doi.org/10.3390/catal10111262.
Повний текст джерелаLin, Yen-Ting, and Sam P. de Visser. "Product Distributions of Cytochrome P450 OleTJE with Phenyl-Substituted Fatty Acids: A Computational Study." International Journal of Molecular Sciences 22, no. 13 (July 2, 2021): 7172. http://dx.doi.org/10.3390/ijms22137172.
Повний текст джерелаShang, Ming, Qian Shao, Shang-Zheng Sun, Yan-Qiao Chen, Hui Xu, Hui-Xiong Dai, and Jin-Quan Yu. "Identification of monodentate oxazoline as a ligand for copper-promoted ortho-C–H hydroxylation and amination." Chemical Science 8, no. 2 (2017): 1469–73. http://dx.doi.org/10.1039/c6sc03383k.
Повний текст джерелаLiu, Yunyun, Meiying Huang, and Li Wei. "Copper-catalyzed synthesis of benzo[d][1,3]dioxin-4-ones via tandem Ar–halogen bond hydroxylation and dichloromethane-based double Williamson etherification." New Journal of Chemistry 41, no. 12 (2017): 4776–78. http://dx.doi.org/10.1039/c7nj00180k.
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