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Статті в журналах з теми "Novel reactive intermediates"
Hemberger, Patrick, Jeroen A. van Bokhoven, Javier Pérez-Ramírez, and Andras Bodi. "New analytical tools for advanced mechanistic studies in catalysis: photoionization and photoelectron photoion coincidence spectroscopy." Catalysis Science & Technology 10, no. 7 (2020): 1975–90. http://dx.doi.org/10.1039/c9cy02587a.
Повний текст джерелаDamsten, Micaela C., Jon S. B. de Vlieger, Wilfried M. A. Niessen, Hubertus Irth, Nico P. E. Vermeulen, and Jan N. M. Commandeur. "Trimethoprim: Novel Reactive Intermediates and Bioactivation Pathways by Cytochrome P450s." Chemical Research in Toxicology 21, no. 11 (November 17, 2008): 2181–87. http://dx.doi.org/10.1021/tx8002593.
Повний текст джерелаKessar, S. V. "Lewis acid complexed azacarbanions: Novel reactive intermediates of wide synthetic utility." Pure and Applied Chemistry 68, no. 3 (January 1, 1996): 509–14. http://dx.doi.org/10.1351/pac199668030509.
Повний текст джерелаHansel, Colleen M., Timothy G. Ferdelman, and Bradley M. Tebo. "Cryptic Cross-Linkages Among Biogeochemical Cycles: Novel Insights from Reactive Intermediates." Elements 11, no. 6 (November 30, 2015): 409–14. http://dx.doi.org/10.2113/gselements.11.6.409.
Повний текст джерелаGreen, Justin L., and Gregory A. Reed. "Benzo[a]pyrene bay-region sulfonates, a novel class of reactive intermediates." Chemical Research in Toxicology 3, no. 1 (January 1990): 59–64. http://dx.doi.org/10.1021/tx00013a010.
Повний текст джерелаThome, Ulrich, Ahmed Lazrak, Lan Chen, Marion C. Kirk, Michael J. Thomas, Henry Jay Forman, and Sadis Matalon. "Novel SIN-1 reactive intermediates modulate chloride secretion across murine airway cells." Free Radical Biology and Medicine 35, no. 6 (September 2003): 662–75. http://dx.doi.org/10.1016/s0891-5849(03)00392-7.
Повний текст джерелаAttwa, Mohamed W., Adnan A. Kadi, and Hany W. Darwish. "Belizatinib: Novel reactive intermediates and bioactivation pathways characterized by LC–MS/MS." Journal of Pharmaceutical and Biomedical Analysis 171 (July 2019): 132–47. http://dx.doi.org/10.1016/j.jpba.2019.04.006.
Повний текст джерелаGroves, John T. "Cytochrome P450 enzymes: understanding the biochemical hieroglyphs." F1000Research 4 (July 1, 2015): 178. http://dx.doi.org/10.12688/f1000research.6314.1.
Повний текст джерелаHe, Chao, Galiya R. Galimova, Yuheng Luo, Long Zhao, André K. Eckhardt, Rui Sun, Alexander M. Mebel, and Ralf I. Kaiser. "A chemical dynamics study on the gas-phase formation of triplet and singlet C5H2carbenes." Proceedings of the National Academy of Sciences 117, no. 48 (November 16, 2020): 30142–50. http://dx.doi.org/10.1073/pnas.2019257117.
Повний текст джерелаKotuniak, Radosław, and Wojciech Bal. "Kinetics of Cu(ii) complexation by ATCUN/NTS and related peptides: a gold mine of novel ideas for copper biology." Dalton Transactions 51, no. 1 (2022): 14–26. http://dx.doi.org/10.1039/d1dt02878b.
Повний текст джерелаДисертації з теми "Novel reactive intermediates"
Sasaki, Ikuo. "Development of Novel Synthetic Methods of Organosilicon Compounds Utilizing Silicon-Containing Reactive Intermediates." Kyoto University, 2020. http://hdl.handle.net/2433/253508.
Повний текст джерелаCampbell, Steven John. "Novel methods to characterise atmospherically relevant organic radicals and reactive oxygen species." Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/274099.
Повний текст джерелаHirayama, Lacie C. "Novel reactions of organoindium compounds : the synthesis of chiral alcohols, allylboron reagents and identification of the reactive intermediates /." Diss., Digital Dissertations Database. Restricted to UC campuses, 2007. http://uclibs.org/PID/11984.
Повний текст джерелаMurrin, Andrew T. "N-Glycosyl Aza-Ylides as Intermediates in the Synthesis of Novel N-Glycosides." Youngstown State University / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1590679639104474.
Повний текст джерелаXu, Chang. "A Novel Mass Spectrometry Method to Study Reaction Intermediates and Development of AuTeCDs for Scavenging ROS in Live Cells." Ohio University / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1597326111937675.
Повний текст джерелаWelsh, Kevin M. "The generation and characterization of novel organosilicon reactive intermediates 1,4-disilabenzenes, di-tert-butylsilylene and N, N'-di-tert-butylsilanediimine /." 1987. http://catalog.hathitrust.org/api/volumes/oclc/16004488.html.
Повний текст джерелаSun, Kuo-Hui, та 孫國惠. "Ene Reaction with Pummerer-type Reaction Intermediate of α-( Methylthio)acetic Acid Pyrrolidide : A Novel Synthesis of Trichonine". Thesis, 1998. http://ndltd.ncl.edu.tw/handle/09339185613058770651.
Повний текст джерела高雄醫學院
藥學研究所
86
Dienamide 基團在許多天然物成份中是很重要的結構特徵,曾有報告指 出 dienamide具生理活性,尤其是可做為殺蟲劑。而由 P. trichostachyon leaves 所分離出來的Trichonine [(E,E)-2,4- eicosadienoic acid pyrrolidide] 即是一種含有殺蟲效果的化合物,它 曾經由 Wittig 反應及脫去反應合成出來。本計劃分別利用 methyl α-( methylthio)acetate 及 α-(methylthio)acetic acid pyrrolidide 當 原料,和高價碘試劑 phenyliodine(III) bis(trifluoroacetate) (PIFA) 反應,形成 Pummerer-type 反應中間體,然後與烯類進行 ene 反應來合成 Trichonine。 The dienamide group is an important structural feature of a number of naturalproducts, which have been reported to be biologically active, especially as insecticides. Trichonine [(E, E)-2,4-eicosadienoic acid pyrrolidide] is an insecticidal compound isolated from P. trichostachyon leaves, has been synth- esized by Wittig reaction and elimination reaction. In this work we wish toreport that the Pummerer-type reaction intermediate derived from α-(methylt-hio)acetic acid pyrrolidide and phenyliodine(III) bis(trifluoroacetate) (PIFA)undergoes an ene reaction with 1-alkenes to give the ene adducts and its app- lication to the synthesis of Trichonine.
Zhang, Ji. "The synthesis of several novel non-benzenoid aromatic compounds by use of thiophene intermediates and annulene coupling reaction." Thesis, 1997. https://dspace.library.uvic.ca//handle/1828/9795.
Повний текст джерелаGraduate
Частини книг з теми "Novel reactive intermediates"
Logan, C. J., D. Hesk, and D. H. Hutson. "The Fate of 4-Cyanoacetanilide in Rats and Mice: The Mechanism of Formation of a Novel Electrophilic Metabolite." In Biological Reactive Intermediates III, 749–53. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-5134-4_69.
Повний текст джерелаTreacy, S., X. Zhang, and T. Rovis. "1.13 Intramolecular Hydrogen-Atom Transfer." In Free Radicals: Fundamentals and Applications in Organic Synthesis 1. Stuttgart: Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/sos-sd-234-00299.
Повний текст джерелаBarton, Derek H. R., and Shyamal I. Parekh. "Novel – and – Bond Metatheses.: Mechanistic Probes, Spectroscopic Studies, and Structural Evidence for Reactive Oligomeric Selenoazyl Intermediates." In World Scientific Series in 20th Century Chemistry, 533–39. WORLD SCIENTIFIC / IMPERIAL COLLEGE PRESS, 1996. http://dx.doi.org/10.1142/9789812795984_0090.
Повний текст джерелаRademann, Jörg. "Advanced Polymer Reagents Based on Activated Reactants and Reactive Intermediates: Powerful Novel Tools in Diversity-Oriented Synthesis." In Methods in Enzymology, 366–90. Elsevier, 2003. http://dx.doi.org/10.1016/s0076-6879(03)69020-8.
Повний текст джерелаTaber, Douglass. "Intermolecular and Intramolecular Diels-Alder Reactions: (-)-Oseltamivir (Fukuyama), Platensimycin (Yamamoto) and 11,12-Diacetoxydrimane (Jacobsen)." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0078.
Повний текст джерелаSheppard, R. C. "Introduction — a retrospective viewpoint." In Fmoc Solid Phase Peptide Synthesis. Oxford University Press, 1999. http://dx.doi.org/10.1093/oso/9780199637256.003.0005.
Повний текст джерелаTaber, Douglass. "Enantioselective Assembly of Oxygenated Stereogenic Centers." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0032.
Повний текст джерелаТези доповідей конференцій з теми "Novel reactive intermediates"
Rajagopalan, Raghavan, Amol Karwa, Przemyslaw M. Lusiak, Kripa Srivastava, Amruta R. Poreddy, Raghootama S. Pandurangi, Karen P. Galen, William L. Neumann, Gary E. Cantrell, and Richard B. Dorshow. "Novel type 1 photosensitizers: viability of leukemia cells exposed to reactive intermediates generated in situ by in vitro photofragmentation." In 12th World Congress of the International Photodynamic Association, edited by David H. Kessel. SPIE, 2009. http://dx.doi.org/10.1117/12.822840.
Повний текст джерелаPine, Thomas, Anh-Tuan V. Do, Li Zhao, and Jacob Brouwer. "Operation of a Novel Dry Hydrocarbon Tolerant Intermediate Temperature Solid Oxide Fuel Cell." In ASME 2009 7th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2009. http://dx.doi.org/10.1115/fuelcell2009-85094.
Повний текст джерелаZhang, Xiaodong, Min Xu, Li Sun, Rongfeng Sun, Feipeng Cai, and Dongyan Guo. "Biomass Gasification for Syngas Production." In ASME Turbo Expo 2006: Power for Land, Sea, and Air. ASMEDC, 2006. http://dx.doi.org/10.1115/gt2006-90591.
Повний текст джерелаWong, Chee Wah, Nicolas Sluys, Mohd Khirfan, Nitheesh Kumar Unnikrishnan, Saleh Al Ameri, and Sultan Mohamed Al Yamani. "A Novel Engineered Drilling Solution for Improving Backreaming and Drilling Efficiency." In ADIPEC. SPE, 2022. http://dx.doi.org/10.2118/211787-ms.
Повний текст джерелаLozza, Giovanni, Paolo Chiesa, Matteo Romano, and Paolo Savoldelli. "Three Reactors Chemical Looping Combustion for High Efficiency Electricity Generation With CO2 Capture From Natural Gas." In ASME Turbo Expo 2006: Power for Land, Sea, and Air. ASMEDC, 2006. http://dx.doi.org/10.1115/gt2006-90345.
Повний текст джерелаTripathi, Abhinav, Chen Zhang, and Zongxuan Sun. "Experimental Investigation and Analysis of Auto-Ignition Combustion Dynamics." In ASME 2018 Dynamic Systems and Control Conference. American Society of Mechanical Engineers, 2018. http://dx.doi.org/10.1115/dscc2018-9184.
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