Artykuły w czasopismach na temat „Alkylation”
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Saini, Natalie, Joan F. Sterling, Cynthia J. Sakofsky, Camille K. Giacobone, Leszek J. Klimczak, Adam B. Burkholder, Ewa P. Malc, Piotr A. Mieczkowski i Dmitry A. Gordenin. "Mutation signatures specific to DNA alkylating agents in yeast and cancers". Nucleic Acids Research 48, nr 7 (5.03.2020): 3692–707. http://dx.doi.org/10.1093/nar/gkaa150.
Pełny tekst źródłaGarcia-Ramos, Yesica, Caroline Proulx i William D. Lubell. "Synthesis of hydrazine and azapeptide derivatives by alkylation of carbazates and semicarbazones". Canadian Journal of Chemistry 90, nr 11 (listopad 2012): 985–93. http://dx.doi.org/10.1139/v2012-070.
Pełny tekst źródłaHadzic, Pavle, Mirjana Popsavin i Suncica Borozan. "Alkylating ability of carbohydrate oxetanes: Practical synthesis of bolaform skeleton derivative". Journal of the Serbian Chemical Society 80, nr 10 (2015): 1273–78. http://dx.doi.org/10.2298/jsc150224033h.
Pełny tekst źródłaMcIntosh, John M., i Pratibha Mishra. "Alkylation of camphor imines of glycinates. Diastereoselectivity as a function of electronic factors in the alkylating agent". Canadian Journal of Chemistry 64, nr 4 (1.04.1986): 726–31. http://dx.doi.org/10.1139/v86-117.
Pełny tekst źródłaShimkin, Kirk W., i Donald A. Watson. "Recent developments in copper-catalyzed radical alkylations of electron-rich π-systems". Beilstein Journal of Organic Chemistry 11 (23.11.2015): 2278–88. http://dx.doi.org/10.3762/bjoc.11.248.
Pełny tekst źródłaPlatzek, T., G. Bochert, U. Rahm i D. Neubert. "Embryotoxicity Induced by Alkylating Agents. Some Methodological Aspects of DNA Alkylation Studies in Murine Embryos Using Ethylmethanesulfonate". Zeitschrift für Naturforschung C 42, nr 5 (1.05.1987): 613–26. http://dx.doi.org/10.1515/znc-1987-0519.
Pełny tekst źródłaGoryunova, Alexandra Konstantinovna, Nina Sergeevna Baklan, Galina Vladimirovna Timofeeva i Elena Vladimirovna Nosova. "Studies of the Purolite CT151DRY alkylation catalyst by Purolite in the phenol alkylation reaction of ethylene oligomers of the C16-C18 fraction". Oil and gas technologies and environmental safety 2023, nr 3 (29.09.2023): 20–26. http://dx.doi.org/10.24143/1812-9498-2023-3-20-26.
Pełny tekst źródłaKaliendina, S., M. Brynzei, M. Kut, S. M. Sukharev, Е. Ostapchuk i M. Onysko. "Kaliendina S., Brynzei M., Kut M., Sukharev S.M., Ostapchuk Е., Onysko M. REGIOSELECTIVITY OF ALKYLATION OF 2-(THIOPHENE-2-IL)THIENO[2,3 d]PYRIMIDINE-4(3H)-ONE". Scientific Bulletin of the Uzhhorod University. Series «Chemistry» 50, nr 2 (22.01.2024): 40–45. http://dx.doi.org/10.24144/2414-0260.2023.2.40-45.
Pełny tekst źródłaAlagoz, Meryem, Owen S. Wells i Sherif F. El-Khamisy. "TDP1 deficiency sensitizes human cells to base damage via distinct topoisomerase I and PARP mechanisms with potential applications for cancer therapy". Nucleic Acids Research 42, nr 5 (12.12.2013): 3089–103. http://dx.doi.org/10.1093/nar/gkt1260.
Pełny tekst źródłaYoshikai, Naohiko, i Ke Gao. "Cobalt-catalyzed directed alkylation of arenes with primary and secondary alkyl halides". Pure and Applied Chemistry 86, nr 3 (20.03.2014): 419–24. http://dx.doi.org/10.1515/pac-2014-5005.
Pełny tekst źródłaFahrer, Jörg, i Markus Christmann. "DNA Alkylation Damage by Nitrosamines and Relevant DNA Repair Pathways". International Journal of Molecular Sciences 24, nr 5 (28.02.2023): 4684. http://dx.doi.org/10.3390/ijms24054684.
Pełny tekst źródłaQian, Bo, Hongli Bao, Yuehua Zeng i Yajun Li. "A Metal-Free Approach for Brønsted Acid Promoted C–H Alkylation of Heteroarenes with Alkyl Peroxides". Synthesis 50, nr 16 (29.05.2018): 3250–56. http://dx.doi.org/10.1055/s-0037-1609965.
Pełny tekst źródłaMemisoglu, Asli, i Leona Samson. "Contribution of Base Excision Repair, Nucleotide Excision Repair, and DNA Recombination to Alkylation Resistance of the Fission Yeast Schizosaccharomyces pombe". Journal of Bacteriology 182, nr 8 (15.04.2000): 2104–12. http://dx.doi.org/10.1128/jb.182.8.2104-2112.2000.
Pełny tekst źródłaSakamoto, Ryu, Shunya Sakurai i Keiji Maruoka. "Bis(trialkylsilyl) peroxides as alkylating agents in the copper-catalyzed selective mono-N-alkylation of primary amides". Chemical Communications 53, nr 48 (2017): 6484–87. http://dx.doi.org/10.1039/c7cc02910a.
Pełny tekst źródłaWei, Yahui, Qingqing Xuan, Yao Zhou i Qiuling Song. "Reductive N-alkylation of primary and secondary amines using carboxylic acids and borazane under mild conditions". Organic Chemistry Frontiers 5, nr 24 (2018): 3510–14. http://dx.doi.org/10.1039/c8qo00942b.
Pełny tekst źródłaChen, Rongzhen, Jin-Tao Yu i Jiang Cheng. "Metal-free oxidative decarbonylative alkylation of chromones using aliphatic aldehydes". Organic & Biomolecular Chemistry 16, nr 19 (2018): 3568–71. http://dx.doi.org/10.1039/c8ob00720a.
Pełny tekst źródłaLi, Dengke, i Xianfu Shen. "Iron-catalyzed regioselective alkylation of 1,4-quinones and coumarins with functionalized alkyl bromides". Organic & Biomolecular Chemistry 18, nr 4 (2020): 750–54. http://dx.doi.org/10.1039/c9ob02289a.
Pełny tekst źródłaStoltz, Brian, Samantha Shockley i J. Hethcox. "Intermolecular Stereoselective Iridium-Catalyzed Allylic Alkylation: An Evolutionary Account". Synlett 29, nr 19 (15.08.2018): 2481–92. http://dx.doi.org/10.1055/s-0037-1610217.
Pełny tekst źródłaSato, Norihiro, Genichiro Tsuji, Yoshihiro Sasaki, Akira Usami, Takuma Moki, Kazumitsu Onizuka, Ken Yamada i Fumi Nagatsugi. "A new strategy for site-specific alkylation of DNA using oligonucleotides containing an abasic site and alkylating probes". Chemical Communications 51, nr 80 (2015): 14885–88. http://dx.doi.org/10.1039/c5cc03915k.
Pełny tekst źródłaBouziane, M., F. Miao, N. Ye, G. Holmquist, G. Chyzak i T. R. O'Connor. "Repair of DNA alkylation damage." Acta Biochimica Polonica 45, nr 1 (31.03.1998): 191–202. http://dx.doi.org/10.18388/abp.1998_4333.
Pełny tekst źródłaSchönbauer, David, Manuel Spettel, Robert Pollice, Ernst Pittenauer i Michael Schnürch. "Investigations of the generality of quaternary ammonium salts as alkylating agents in direct C–H alkylation reactions: solid alternatives for gaseous olefins". Organic & Biomolecular Chemistry 17, nr 16 (2019): 4024–30. http://dx.doi.org/10.1039/c9ob00243j.
Pełny tekst źródłaMo, Fanyang, i Guangbin Dong. "Regioselective ketone α-alkylation with simple olefins via dual activation". Science 345, nr 6192 (3.07.2014): 68–72. http://dx.doi.org/10.1126/science.1254465.
Pełny tekst źródłaLambert, Georg, Ian C. Forster, Gerti Stange, Jürg Biber i Heini Murer. "Properties of the Mutant Ser-460-Cys Implicate This Site in a Functionally Important Region of the Type Iia Na+/Pi Cotransporter Protein". Journal of General Physiology 114, nr 5 (11.10.1999): 637–52. http://dx.doi.org/10.1085/jgp.114.5.637.
Pełny tekst źródłaHume, Paul A., Margaret A. Brimble i Jóhannes Reynisson. "The Bioreductive Alkylation of DNA by Kalafungin: A Theoretical Investigation". Australian Journal of Chemistry 65, nr 4 (2012): 402. http://dx.doi.org/10.1071/ch12018.
Pełny tekst źródłaXu, Qing, Huamei Xie, Er-Lei Zhang, Xiantao Ma, Jianhui Chen, Xiao-Chun Yu i Huan Li. "Selective catalytic Hofmann N-alkylation of poor nucleophilic amines and amides with catalytic amounts of alkyl halides". Green Chemistry 18, nr 14 (2016): 3940–44. http://dx.doi.org/10.1039/c6gc00938g.
Pełny tekst źródłaMeng, Guangrong, Mehulkumar Patel, Feixiang Luo, Qingdong Li, Carol Flach, Richard Mendelsohn, Eric Garfunkel, Huixin He i Michal Szostak. "Graphene oxide catalyzed ketone α-alkylation with alkenes: enhancement of graphene oxide activity by hydrogen bonding". Chemical Communications 55, nr 37 (2019): 5379–82. http://dx.doi.org/10.1039/c9cc02578b.
Pełny tekst źródłaBegleiter, Asher. "The contribution of alkylation to the activity of quinone antitumor agents". Canadian Journal of Physiology and Pharmacology 64, nr 5 (1.05.1986): 581–85. http://dx.doi.org/10.1139/y86-096.
Pełny tekst źródłaRamadan, Sayed K., Wael S. I. Abou-Elmagd i Ahmed I. Hashem. "Alkylation of 2(3H)-Furanones: Inter- versus Intra-Molecular". Letters in Organic Chemistry 17, nr 6 (20.05.2020): 430–33. http://dx.doi.org/10.2174/1570178617666191203102528.
Pełny tekst źródłaRana, Jagannath, Virendrakumar Gupta i Ekambaram Balaraman. "Manganese-catalyzed direct C–C coupling of α-C–H bonds of amides and esters with alcohols via hydrogen autotransfer". Dalton Transactions 48, nr 21 (2019): 7094–99. http://dx.doi.org/10.1039/c8dt05020a.
Pełny tekst źródłaKhatri, Praveen K., Manvi Manchanda, Indrajit K. Ghosh i Suman L. Jain. "Polymer impregnated sulfonated carbon composite solid acid catalyst for alkylation of phenol with methyl-tert-butyl ether". RSC Advances 5, nr 5 (2015): 3286–90. http://dx.doi.org/10.1039/c4ra11033a.
Pełny tekst źródłaZhang, Qiao Y., Xin J. Cheng, Xin Y. Zhao, La M. Wu, Long F. Jin i Hui J. Zhang. "Combined Alkylating Agents as a Resolution for Highly Selective N-Alkylation of 2-Hydroxybenzaldehyde Acylhydrazones". Synlett 30, nr 11 (8.05.2019): 1334–38. http://dx.doi.org/10.1055/s-0037-1611823.
Pełny tekst źródłaSamruddhi, Mane, Akash Bhatkar, Marimuthu Prabu, Siva Prasad Mekala, Pranjal Gogoi, Gourab Mohapatra i Raja Thirumalaiswamy. "Selective O-alkylation of Phenol Using Dimethyl Ether". Reactions 3, nr 4 (17.11.2022): 602–14. http://dx.doi.org/10.3390/reactions3040040.
Pełny tekst źródłaLiu, Chang, Jianwei Sun i Pengfei Li. "Chiral Phosphine Catalyzed Allylic Alkylation of Benzylidene Succinimides with Morita–Baylis–Hillman Carbonates". Molecules 28, nr 6 (21.03.2023): 2825. http://dx.doi.org/10.3390/molecules28062825.
Pełny tekst źródłaKeglevich, György, Nóra Kiss, Alajos Grün, Erika Bálint i Tamara Kovács. "Advantages of the Microwave Tool in Organophosphorus Syntheses". Synthesis 49, nr 14 (20.06.2017): 3069–83. http://dx.doi.org/10.1055/s-0036-1589031.
Pełny tekst źródłaXu, Di, Lena Frank, Tina Nguyen, Andreas Stumpf, David Russell, Remy Angelaud i Francis Gosselin. "Magnesium-Catalyzed N2-Regioselective Alkylation of 3-Substituted Pyrazoles". Synlett 31, nr 06 (9.08.2019): 595–99. http://dx.doi.org/10.1055/s-0039-1690160.
Pełny tekst źródłaMijin, Dusan, Milica Misic-Vukovic i Slobodan Petrovic. "Alkylation of N-substituted-2-phenylacetamides". Journal of the Serbian Chemical Society 69, nr 10 (2004): 711–36. http://dx.doi.org/10.2298/jsc0410711m.
Pełny tekst źródłaGogoi, Dipanta, Lalmalsawm tluangi i Zodinpuia Pachuau. "Theoretical Study on the Mechanism of Alkylation At 0-6 Position of Guanine by Temozolomide and Bitc-Temozolomide". Science & Technology Journal 6, nr 2 (1.07.2018): 68–74. http://dx.doi.org/10.22232/stj.2018.06.02.12.
Pełny tekst źródłaOnizuka, Kazumitsu, Madoka E. Hazemi, Norihiro Sato, Gen-ichiro Tsuji, Shunya Ishikawa, Mamiko Ozawa, Kousuke Tanno, Ken Yamada i Fumi Nagatsugi. "Reactive OFF-ON type alkylating agents for higher-ordered structures of nucleic acids". Nucleic Acids Research 47, nr 13 (12.06.2019): 6578–89. http://dx.doi.org/10.1093/nar/gkz512.
Pełny tekst źródłaKhlebnikova, Elena, Irena Dolganova, Elena Ivashkina i Stanislav Koshkin. "Modeling of Benzene with Ethylene Alkylation". International Journal of Chemical Engineering and Applications 8, nr 1 (luty 2017): 61–66. http://dx.doi.org/10.18178/ijcea.2017.8.1.631.
Pełny tekst źródłaYudovin-Farber, Ira, Jacob Golenser, Nurit Beyth, Ervin I. Weiss i Abraham J. Domb. "Quaternary Ammonium Polyethyleneimine: Antibacterial Activity". Journal of Nanomaterials 2010 (2010): 1–11. http://dx.doi.org/10.1155/2010/826343.
Pełny tekst źródłaMorales-Ríos, Martha S., Ernesto Rivera-Becerril, Daphne E. González-Juárez, Juan Benjamín García-Vázquez, Joel J. Trujillo-Serrato, Angelina Hernández-Barragán i Pedro Joseph-Nathan. "Synthesis of Pyrrolidinoindolines from 2-(2-Oxo-3-indolyl)acetates: Scope and Limitations". Natural Product Communications 6, nr 4 (kwiecień 2011): 1934578X1100600. http://dx.doi.org/10.1177/1934578x1100600406.
Pełny tekst źródłaZhao, Zhensheng, Islam Jameel i Graham K. Murphy. "Vicinal Dichlorination of o-Vinylbiphenyls and the Synthesis of 9-(Arylmethyl)fluorenes via Tandem Friedel–Crafts Alkylations". Synthesis 51, nr 13 (28.05.2019): 2648–59. http://dx.doi.org/10.1055/s-0037-1611562.
Pełny tekst źródłaLiu, Tinglan, Yu Zhou, Junhong Tang i Chengming Wang. "Recent advancements in iodide/phosphine-mediated photoredox radical reactions". Beilstein Journal of Organic Chemistry 19 (22.11.2023): 1785–803. http://dx.doi.org/10.3762/bjoc.19.131.
Pełny tekst źródłaAraujo-Lima, Carlos F., Larissa S. A. Christoni, Graça Justo, Maria N. C. Soeiro, Claudia A. F. Aiub i Israel Felzenszwalb. "Atorvastatin Downregulates In Vitro Methyl Methanesulfonate and Cyclophosphamide Alkylation-Mediated Cellular and DNA Injuries". Oxidative Medicine and Cellular Longevity 2018 (2018): 1–11. http://dx.doi.org/10.1155/2018/7820890.
Pełny tekst źródłaShunkevich, A. A., A. P. Polikarpov, G. V. Medyak, S. D. Filippovich i Z. I. Akulich. "Synthesis and properties of new strongly basic fibrous anion exchangers". Proceedings of the National Academy of Sciences of Belarus, Chemical Series 58, nr 3 (7.09.2022): 286–93. http://dx.doi.org/10.29235/1561-8331-2022-58-3-286-293.
Pełny tekst źródłaAllocca, Mariacarmela, Joshua J. Corrigan, Aprotim Mazumder, Kimberly R. Fake i Leona D. Samson. "Inflammation, necrosis, and the kinase RIP3 are key mediators of AAG-dependent alkylation-induced retinal degeneration". Science Signaling 12, nr 568 (12.02.2019): eaau9216. http://dx.doi.org/10.1126/scisignal.aau9216.
Pełny tekst źródłaPosnick, Lauren M., i Leona D. Samson. "Influence of S-Adenosylmethionine Pool Size on Spontaneous Mutation, Dam Methylation, and Cell Growth ofEscherichia coli". Journal of Bacteriology 181, nr 21 (1.11.1999): 6756–62. http://dx.doi.org/10.1128/jb.181.21.6756-6762.1999.
Pełny tekst źródłaAikawa, Haruo, Tetsuro Kaneko, Naoki Asao i Yoshinori Yamamoto. "Gold-catalyzed alkylation of silyl enol ethers with ortho-alkynylbenzoic acid esters". Beilstein Journal of Organic Chemistry 7 (20.05.2011): 648–52. http://dx.doi.org/10.3762/bjoc.7.76.
Pełny tekst źródłaDong, Guangbin, Hee Lim i Dong Xing. "Transition-Metal-Catalyzed Ketone α-Alkylation and Alkenylation with Simple Alkenes and Alkynes through a Dual Activation Strategy". Synlett 30, nr 06 (21.11.2018): 674–84. http://dx.doi.org/10.1055/s-0037-1610315.
Pełny tekst źródłaSandhu, Navjot, Simran Madaan, Satish K. Pandey, Amritpal Singh, Kamlesh Kumar, Rajesh K. Yadav, Rahul Shrivastava i Atul P. Singh. "Experimental and theoretical observations of alkylated EOSIN based “turn-on” superoxide sensor as well as its anti-microbial study". Main Group Chemistry 20, nr 4 (22.12.2021): 623–32. http://dx.doi.org/10.3233/mgc-210068.
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