Статті в журналах з теми "Morpholino Chemistry"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Morpholino Chemistry".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.
Huber, Gerald, Annette Schier, and Hubert Schmidbaur. "The Stereochemistry of Chloro-bis(N-morpholino)phenylsilane." Zeitschrift für Naturforschung B 54, no. 1 (January 1, 1999): 18–20. http://dx.doi.org/10.1515/znb-1999-0106.
Повний текст джерелаPaul, Sibasish, and Marvin H. Caruthers. "Synthesis of Backbone-Modified Morpholino Oligonucleotides Using Phosphoramidite Chemistry." Molecules 28, no. 14 (July 13, 2023): 5380. http://dx.doi.org/10.3390/molecules28145380.
Повний текст джерелаHao, Xue-chen, Jiu-fu Lu, Ye Chen, Yang Wang, Shi Ding, and Ju Liu. "Synthesis, Crystal Structure and Antitumour Activity of 3-Amino-N-(5-Fluoro-2-Methylphenyl)-4-Morpholino-1H-Indazole-1-Carboxamide." Journal of Chemical Research 41, no. 11 (November 2017): 624–26. http://dx.doi.org/10.3184/174751917x15065183733178.
Повний текст джерелаTang, Zhi-hua, and Wei-Jun Fu. "Synthesis, Crystal Structure and Antitumour Activity of 3-Amino-4-Morpholino-1H-Indazol-1-yl(3-Fluorophenyl)Methanone." Journal of Chemical Research 42, no. 11 (November 2018): 552–55. http://dx.doi.org/10.3184/174751918x15402939385990.
Повний текст джерелаLu, Jiu-fu, Ling-xia Jin, Hong-guang Ge, Juan Song, Cai-bin Zhao, Xiao-hua Guo, Si-yu Yue, and Li Li. "Synthesis, Crystal Structure and Antitumour Activity of 4-(3-Amino-4-Morpholino-1H-Indazole-1-Carbonyl)Benzonitrile." Journal of Chemical Research 42, no. 6 (June 2018): 309–12. http://dx.doi.org/10.3184/174751918x15287920661730.
Повний текст джерелаJi, Xiao-hui, Ling-xia Jin, Cai-bin Zhao, Nan Zheng, Juan Song, Hong-guang Ge, Quan Liu, and Jiu-fu Lu. "Synthesis, Crystal Structure and Antitumour Activity of 3-Amino-N-[4-chloro-3-(Trifluoromethyl)Phenyl]-4-Morpholino-1H-Indazole-1-Carboxamide." Journal of Chemical Research 42, no. 10 (October 2018): 504–7. http://dx.doi.org/10.3184/174751918x15380423621264.
Повний текст джерелаLu, Jiu-fu, Xing-long Zhou, Yu-hang Xu, Si-yu Yue, Xiao-hui Ji, Nan Zheng, and Ling-xia Jin. "Synthesis, Crystal Structure, and Biological Activity of 3-Amino-4-Morpholino-N-[2-(Trifluoromethoxy)Phenyl]-1H-Indazole-1-Carboxamide." Journal of Chemical Research 41, no. 9 (September 2017): 526–28. http://dx.doi.org/10.3184/174751917x15033157981988.
Повний текст джерелаRádl, Stanislav, and Pavel Hradil. "Synthesis of some 1-alkyl-1,4-dihydro-4-oxo-1,7-naphthyridine-3-carboxylic acids." Collection of Czechoslovak Chemical Communications 56, no. 11 (1991): 2420–29. http://dx.doi.org/10.1135/cccc19912420.
Повний текст джерелаTiravia, Martina, Federica Sabuzi, Francesca Valentini, Valeria Conte, and Pierluca Galloni. "3-Morpholino-7-[N-methyl-N-(4′-carboxyphenyl)amino]phenothiazinium Chloride." Molbank 2022, no. 4 (November 14, 2022): M1493. http://dx.doi.org/10.3390/m1493.
Повний текст джерелаBasha, S. Farook, and M. Syed Ali Padusha. "Ultrasonic Studies on the Nature of Molecular Interaction of Synthesized Mannich Bases in DMSO at Different Temperatures." Asian Journal of Chemistry 31, no. 4 (February 27, 2019): 960–64. http://dx.doi.org/10.14233/ajchem.2019.21893.
Повний текст джерелаAung-Htut, May T., Craig S. McIntosh, Kristin A. West, Sue Fletcher, and Steve D. Wilton. "In Vitro Validation of Phosphorodiamidate Morpholino Oligomers." Molecules 24, no. 16 (August 12, 2019): 2922. http://dx.doi.org/10.3390/molecules24162922.
Повний текст джерелаMin, So Jeong, Na Young Kim, Hyun Young Chae, and Keun Ho Chun. "Diastereoselective Synthesis of Phosphorodiamidate Morpholino Dimers." Bulletin of the Korean Chemical Society 41, no. 3 (February 11, 2020): 252–53. http://dx.doi.org/10.1002/bkcs.11958.
Повний текст джерелаDostál, Jiří, Milan Potáček, and Miloslav Nechvátal. "Reactions of 5-Methylphenanthridinium Iodide with Nucleophiles and Reaction Products Conversion." Collection of Czechoslovak Chemical Communications 58, no. 2 (1993): 395–403. http://dx.doi.org/10.1135/cccc19930395.
Повний текст джерелаLeventić, Marijana, Teuta Opačak-Bernardi, Vesna Rastija, Josipa Matić, Dijana Pavlović Saftić, Željka Ban, Biserka Žinić, and Ljubica Glavaš-Obrovac. "The Mechanism of Anti-Tumor Activity of 6-Morpholino- and 6-Amino-9-Sulfonylpurine Derivatives on Human Leukemia Cells." Molecules 28, no. 16 (August 19, 2023): 6136. http://dx.doi.org/10.3390/molecules28166136.
Повний текст джерелаBonacorso, Helio G., Melissa B. Rodrigues, Bernardo A. Iglesias, Carolina H. da Silveira, Sarah C. Feitosa, Wilian C. Rosa, Marcos A. P. Martins, Clarissa P. Frizzo, and Nilo Zanatta. "New 2-(aryl/heteroaryl)-6-(morpholin-4-yl/pyrrolidin-1-yl)-(4-trifluoromethyl)quinolines: synthesis via Buchwald–Hartwig amination, photophysics, and biomolecular binding properties." New Journal of Chemistry 42, no. 12 (2018): 10024–35. http://dx.doi.org/10.1039/c8nj01120f.
Повний текст джерелаMcIntosh, Craig S., May Thandar Aung-Htut, Sue Fletcher, and Steve D. Wilton. "Removal of the Polyglutamine Repeat of Ataxin-3 by Redirecting pre-mRNA Processing." International Journal of Molecular Sciences 20, no. 21 (October 31, 2019): 5434. http://dx.doi.org/10.3390/ijms20215434.
Повний текст джерелаIslas-Jácome, Perla, Cecilia García-Falcón, Sandra L. Castañón-Alonso, Ernesto Calderón-Jaimes, Daniel Canseco-González, Alejandro Islas-Jácome, and Eduardo González-Zamora. "2-Benzyl-7-(4-chlorophenyl)-3-morpholino-6-((1-phenyl-1H-1,2,3-triazol-4-yl)methyl)-6,7-dihydro-5H-pyrrolo[3,4-b]pyridin-5-one." Molbank 2023, no. 3 (July 10, 2023): M1693. http://dx.doi.org/10.3390/m1693.
Повний текст джерелаBucci, Raffaella, Alessandro Contini, Francesca Clerici, Sara Pellegrino та Maria Luisa Gelmi. "From glucose to enantiopure morpholino β-amino acid: a new tool for stabilizing γ-turns in peptides". Organic Chemistry Frontiers 6, № 7 (2019): 972–82. http://dx.doi.org/10.1039/c8qo01116h.
Повний текст джерелаPaul, Sibasish, and Marvin H. Caruthers. "Synthesis of Phosphorodiamidate Morpholino Oligonucleotides and Their Chimeras Using Phosphoramidite Chemistry." Journal of the American Chemical Society 138, no. 48 (November 14, 2016): 15663–72. http://dx.doi.org/10.1021/jacs.6b08854.
Повний текст джерелаBös, Markus, Marcus Herbig, Uwe Böhme, and Edwin Kroke. "Syntheses and molecular structures of some di(amidino)monosilanes." Main Group Metal Chemistry 44, no. 1 (January 1, 2021): 228–38. http://dx.doi.org/10.1515/mgmc-2021-0024.
Повний текст джерелаSadikov, K. D., A. S. Smirnov, S. V. Makarenko, and V. M. Berestovitskaya. "Synthesis of 2-morpholino(piperidino)-3-nitroacrylates." Russian Journal of Organic Chemistry 40, no. 10 (October 2004): 1544–45. http://dx.doi.org/10.1007/s11178-005-0061-x.
Повний текст джерелаLai, Chin-Hung, Chia-Chin Chang, Yi-Lin Weng, and Ta-Hsien Chuang. "Synthesis, Experimental and Density Functional Theory (DFT) Studies on Solubility of Camptothecin Derivatives." Molecules 23, no. 12 (December 1, 2018): 3170. http://dx.doi.org/10.3390/molecules23123170.
Повний текст джерелаPalframan, Matthew J., Rima D. Alharthy, Paulina K. Powalowska, and Christopher J. Hayes. "Synthesis of triazole-linked morpholino oligonucleotides via CuI catalysed cycloaddition." Organic & Biomolecular Chemistry 14, no. 11 (2016): 3112–19. http://dx.doi.org/10.1039/c6ob00007j.
Повний текст джерелаGong, Ping, Kang Wang, Yatao Liu, Kenneth Shepard, and Rastislav Levicky. "Molecular Mechanisms in Morpholino−DNA Surface Hybridization." Journal of the American Chemical Society 132, no. 28 (July 21, 2010): 9663–71. http://dx.doi.org/10.1021/ja100881a.
Повний текст джерелаLiu, Yatao, Damion Irving, Wanqiong Qiao, Dongbiao Ge, and Rastislav Levicky. "Kinetic Mechanisms in Morpholino–DNA Surface Hybridization." Journal of the American Chemical Society 133, no. 30 (August 3, 2011): 11588–96. http://dx.doi.org/10.1021/ja202631b.
Повний текст джерелаRatemi, Elaref S., Nivedita Namdev, and Martin S. Gibson. "Pyridine and pyrimidine ring syntheses from 4-(4-morpholino)-3-pentenone and from ethyl 3-(4-morpholino)-2-butenoate." Journal of Heterocyclic Chemistry 30, no. 6 (December 1993): 1513–16. http://dx.doi.org/10.1002/jhet.5570300609.
Повний текст джерелаNaumczuk, B., R. Kawęcki, J. Sitkowski, W. Bocian, E. Bednarek, and L. Kozerski. "Spontaneous 2′-deoxyguanosine alkylation by a new generation of topoisomerase I inhibitors of the camptothecin family." New Journal of Chemistry 40, no. 4 (2016): 3010–13. http://dx.doi.org/10.1039/c5nj03497c.
Повний текст джерелаMaas, Gerhard, and Theo Mayer. "The Organocopper Route from (2-Propynylidene)morpholinium Triflates to Morpholinoallenes, 1-Morpholino-1,3-butadienes, and 2-Morpholino-1,3-butadienes." Synthesis 1991, no. 12 (1991): 1209–15. http://dx.doi.org/10.1055/s-1991-28421.
Повний текст джерелаWeber, Gunther, Jürgen Hartung, and Lothar Beyer. "Umsetzungen von N-(Morpholino-thocarbonyl)-benzimidchlorid mit Dinucleophilen." Zeitschrift für Chemie 26, no. 2 (August 31, 2010): 70–71. http://dx.doi.org/10.1002/zfch.19860260213.
Повний текст джерелаZhang, Nan, Chunyan Tan, Puqin Cai, Yuyang Jiang, Peizhuo Zhang, and Yufen Zhao. "Synthesis and properties of morpholino chimeric oligonucleotides." Tetrahedron Letters 49, no. 22 (May 2008): 3570–73. http://dx.doi.org/10.1016/j.tetlet.2008.04.035.
Повний текст джерелаAnderluh, Marko. "An improved synthesis of morpholino-glycoamino acids." Tetrahedron Letters 47, no. 52 (December 2006): 9203–6. http://dx.doi.org/10.1016/j.tetlet.2006.10.133.
Повний текст джерелаKamsani, Supriya, Sumathi Vodnala, A. K. D. Bhavani, and Nagamani Rayala. "Design and Synthesis of Novel Bis-Morpholinotriazine Analogs and their Antibacterial, Antifungal and Antioxidant Studies." Asian Journal of Chemistry 34, no. 3 (2022): 720–26. http://dx.doi.org/10.14233/ajchem.2022.23656.
Повний текст джерелаChen, Jianbin, Jikui Wu, and Yunhan Hong. "The morpholino molecular beacon for specific RNA visualization in vivo." Chemical Communications 52, no. 15 (2016): 3191–94. http://dx.doi.org/10.1039/c5cc07124k.
Повний текст джерелаPaul, Sibasish, and Marvin H. Caruthers. "Retraction of “Synthesis of Phosphorodiamidate Morpholino Oligonucleotides and Their Chimeras Using Phosphoramidite Chemistry”." Journal of the American Chemical Society 141, no. 23 (May 30, 2019): 9430. http://dx.doi.org/10.1021/jacs.7b04308.
Повний текст джерелаLiao, Tangbin, Xiaorui Li, Qian Tong, Kai Zou, Hang Zhang, Lina Tang, Zhongyue Sun, and Guo-Jun Zhang. "Ultrasensitive Detection of MicroRNAs with Morpholino-Functionalized Nanochannel Biosensor." Analytical Chemistry 89, no. 10 (April 28, 2017): 5511–18. http://dx.doi.org/10.1021/acs.analchem.7b00487.
Повний текст джерелаBorowiecki, Paweł. "Chemoenzymatic Synthesis of Optically Active Ethereal Analog of iso-Moramide—A Novel Potentially Powerful Analgesic †." International Journal of Molecular Sciences 23, no. 19 (October 5, 2022): 11803. http://dx.doi.org/10.3390/ijms231911803.
Повний текст джерелаGRAY, C., and K. PHILP. "Hydrodynamic and other properties of poly(morpholino)alginamide (PMA)." Carbohydrate Polymers 25, no. 1 (1994): 39–44. http://dx.doi.org/10.1016/0144-8617(94)90160-0.
Повний текст джерелаLangner, Heera K., Katarzyna Jastrzebska, and Marvin H. Caruthers. "Synthesis and Characterization of Thiophosphoramidate Morpholino Oligonucleotides and Chimeras." Journal of the American Chemical Society 142, no. 38 (August 31, 2020): 16240–53. http://dx.doi.org/10.1021/jacs.0c04335.
Повний текст джерелаWieczorek, Micha? W., Wies?aw R. Majzner, Renata Kaczmarek, Janina Baraniak, and Wojciech J. Stec. "Crystal and molecular structures of isomeric 2-morpholino-2-thiono-4-methyl-1,3,2-dioxaphosphinane and 2-morpholino-2-oxo-4-methyl-1,3,2-dioxaphosphinane." Heteroatom Chemistry 9, no. 2 (1998): 271–79. http://dx.doi.org/10.1002/(sici)1098-1071(1998)9:2<271::aid-hc24>3.0.co;2-n.
Повний текст джерелаHauck, Laura, Dan Mourich, and Patrick Iversen. "Analysis of phosphorodiamidate morpholino oligomer chemisrty CpG effects in murine and human cells (158.12)." Journal of Immunology 186, no. 1_Supplement (April 1, 2011): 158.12. http://dx.doi.org/10.4049/jimmunol.186.supp.158.12.
Повний текст джерелаJanaswamy, Srinivas, G. Sreenivasa Murthy, T. Mohan, and M. N. Sudheendra Rao. "Crystal structure analysis of (Morpholino)(Phenyl)(Dicyclohexylamino) phosphiniminocyclotrithiazene." Crystallography Reports 48, no. 1 (January 2003): 68–72. http://dx.doi.org/10.1134/1.1541746.
Повний текст джерелаUkhin, L. Yu, L. V. Belousova, Zh I. Orlova, O. Ya Borbulevych, and O. V. Shishkin. "Reactions of 4-morpholino-1,2-naphthoquinone with enamines ando-phenylenediamine." Russian Chemical Bulletin 49, no. 4 (April 2000): 732–35. http://dx.doi.org/10.1007/bf02495492.
Повний текст джерелаBell, Neil M, Raymond Wong, and Jason Micklefield. "A Non-Enzymatic, DNA Template-Directed Morpholino Primer Extension Approach." Chemistry - A European Journal 16, no. 7 (February 15, 2010): 2026–30. http://dx.doi.org/10.1002/chem.200902237.
Повний текст джерелаTAYYAB, SAAD, TUAN NOR NAZIAN TUAN MAT, and ADYANI AZIZAH ABD HALIM. "DIFFERENTIAL STABILIZING EFFECTS OF BUFFERS ON STRUCTURAL STABILITY OF BOVINE SERUM ALBUMIN AGAINST UREA DENATURATION." Latin American Applied Research - An international journal 52, no. 1 (January 1, 2022): 7–13. http://dx.doi.org/10.52292/j.laar.2022.738.
Повний текст джерелаSedlárová, Eva, Jozef Čižmárik, Dana Novosedlíková, Katarína Podhorová, Lucia Šranková, and Andrej Šrank. "Dependence of log k Obtained by HPLC on log P'exp in the Series Piperidino and Morpholinoethyl Esters of o-, m- and p-Alkoxy Substituted Phenylcarbamic Acids." Collection of Czechoslovak Chemical Communications 58, no. 2 (1993): 310–14. http://dx.doi.org/10.1135/cccc19930310.
Повний текст джерелаSherstyuk, Yuliya V., Nikita V. Ivanisenko, Alexandra L. Zakharenko, Maria V. Sukhanova, Roman Y. Peshkov, Ilia V. Eltsov, Mikhail M. Kutuzov, et al. "Design, Synthesis and Molecular Modeling Study of Conjugates of ADP and Morpholino Nucleosides as A Novel Class of Inhibitors of PARP-1, PARP-2 and PARP-3." International Journal of Molecular Sciences 21, no. 1 (December 27, 2019): 214. http://dx.doi.org/10.3390/ijms21010214.
Повний текст джерелаLemeer, Simone, Chris Jopling, Joost Gouw, Shabaz Mohammed, Albert J. R. Heck, Monique Slijper, and Jeroen den Hertog. "Comparative Phosphoproteomics of Zebrafish Fyn/Yes Morpholino Knockdown Embryos." Molecular & Cellular Proteomics 7, no. 11 (June 11, 2008): 2176–87. http://dx.doi.org/10.1074/mcp.m800081-mcp200.
Повний текст джерелаHermecz, István, Andrea Sánta-Csutor, Csaba Gönczi, Gergely Héja, Éva Csikós, Kálmán Simon, Ágota Smelkó-Esek, and Benjámin Podányi. "Chemical development of the vasopressin receptor 2 antagonist SR-121463." Pure and Applied Chemistry 73, no. 9 (September 1, 2001): 1401–9. http://dx.doi.org/10.1351/pac200173091401.
Повний текст джерелаBhat, Balkrishen, and A. P. Bhaduri. "Grignard Reaction of 2-Substituted-3-Cyanoquinolines." Zeitschrift für Naturforschung B 40, no. 7 (July 1, 1985): 990–95. http://dx.doi.org/10.1515/znb-1985-0724.
Повний текст джерелаSlepukhin, P. A., L. N. Bazhenova, E. B. Letova, and V. I. Filyakova. "X-ray crystallographic study of 2-morpholino-5-trifluoromethyl-1,3,4-thiadiazole." Journal of Structural Chemistry 56, no. 7 (December 2015): 1415–16. http://dx.doi.org/10.1134/s0022476615070252.
Повний текст джерела