Статті в журналах з теми "Coumarin ring"
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Prahadeesh, N., Maheswaran Sithambaresan, and Umaramani Mathiventhan. "A Study on Hydrogen Peroxide Scavenging Activity and Ferric Reducing Ability of Simple Coumarins." Emerging Science Journal 2, no. 6 (December 13, 2018): 417. http://dx.doi.org/10.28991/esj-2018-01161.
Повний текст джерелаMohan, Resmi, M. Vidhyalakshmi, and Venkatasubramanian Sivakumar. "Microwave Assisted Rapid Extraction and Characterization of Coumarin from Fig Plant (Ficus carica)." Asian Journal of Science and Applied Technology 8, no. 1 (May 5, 2019): 1–4. http://dx.doi.org/10.51983/ajsat-2019.8.1.1043.
Повний текст джерелаYoon, Jeong A., and Young Taek Han. "Efficient Synthesis of Pyrido[3,2-c]coumarins via Silver Nitrate Catalyzed Cycloisomerization and Application to the First Synthesis of Polyneomarline C." Synthesis 51, no. 24 (September 30, 2019): 4611–18. http://dx.doi.org/10.1055/s-0037-1610730.
Повний текст джерелаKumari, Sumita, Amit Sharma, and Sonia Yadav. "Pharmacological Potential of Coumarin-Based Derivatives: (A Comprehensive Brief Review)." Oriental Journal Of Chemistry 39, no. 3 (June 30, 2023): 568–76. http://dx.doi.org/10.13005/ojc/390304.
Повний текст джерелаMedyouni, Rawdha, Olfa Naouali, Naceur HAMDI, and Lassaad Baklouti. "Coumarin phthalonitriles: Synthesis and cation binding properties." JOURNAL OF ADVANCES IN CHEMISTRY 11, no. 4 (March 9, 2015): 3512–18. http://dx.doi.org/10.24297/jac.v11i4.6695.
Повний текст джерелаCheke, Rameshwar S., Harun M. Patel, Vaishali M. Patil, Iqrar Ahmad Ansari, Jaya P. Ambhore, Sachin D. Shinde, Adel Kadri, et al. "Molecular Insights into Coumarin Analogues as Antimicrobial Agents: Recent Developments in Drug Discovery." Antibiotics 11, no. 5 (April 24, 2022): 566. http://dx.doi.org/10.3390/antibiotics11050566.
Повний текст джерелаThakur, Abhinay, Rohit Sharma, Vivek Sheel Jaswal, Eugenie Nepovimova, Ashun Chaudhary, and Kamil Kuca. "Psoralen: A Biologically Important Coumarin with Emerging Applications." Mini-Reviews in Medicinal Chemistry 20, no. 18 (December 7, 2020): 1838–45. http://dx.doi.org/10.2174/1389557520666200429101053.
Повний текст джерелаJalhan, Sunny. "Review Article: Various Biological Activities of Coumarin and Oxadiazole Derivatives." Asian Journal of Pharmaceutical and Clinical Research 10, no. 7 (July 1, 2017): 38. http://dx.doi.org/10.22159/ajpcr.2017.v10i7.18461.
Повний текст джерелаSanaryh Mohammed Al-awad, Leaqaa Abdalredha raheem, and Ausama Ayob Jaccob. "Synthesis and Pharmacological Evaluation of Novel Coumarin Derivatives." International Journal of Research in Pharmaceutical Sciences 11, no. 1 (January 27, 2020): 865–74. http://dx.doi.org/10.26452/ijrps.v11i1.1908.
Повний текст джерелаZeydi, Masoud Mohammadi, Seyed Jafar Kalantarian, and Zahra Kazeminejad. "Overview on developed synthesis procedures of coumarin heterocycles." Journal of the Iranian Chemical Society 17, no. 12 (June 27, 2020): 3031–94. http://dx.doi.org/10.1007/s13738-020-01984-1.
Повний текст джерелаSouza, Simone M. de, Franco Delle Monache, and Artur Smânia. "Antibacterial Activity of Coumarins." Zeitschrift für Naturforschung C 60, no. 9-10 (October 1, 2005): 693–700. http://dx.doi.org/10.1515/znc-2005-9-1006.
Повний текст джерелаOlyaei, Abolfazl, Mahnaz Saraei, and Reyhaneh Khoeiniha. "Catalyst-Free One-Pot Synthesis of Novel Heteroarylamine Substituted Furo[3,2-c]coumarins." Synlett 29, no. 12 (May 17, 2018): 1589–92. http://dx.doi.org/10.1055/s-0036-1591582.
Повний текст джерелаShahi, Akbar Massoumi, Mohammad Nikpassand, and Leila Zare Fekri. "Acidic Ionic Liquid-catalyzed Synthesis of Pyrano[4,3-b]pyran-5(4H)-ones using 4,4,4-trifluoro-1-phenylbutane-1,3-dione as a Building Block." Current Organic Synthesis 17, no. 8 (October 28, 2020): 648–53. http://dx.doi.org/10.2174/1570179417666200520111536.
Повний текст джерелаZhou, Li-Ping, and Ling-Liang Long. "7-Diethylamino-3-{(E)-4-[(E)-2-(pyridin-4-yl)ethenyl]styryl}-2H-chromen-2-one." Acta Crystallographica Section E Structure Reports Online 70, no. 2 (January 22, 2014): o176. http://dx.doi.org/10.1107/s1600536814001123.
Повний текст джерелаEl-Sawy, Eslam Reda, Ahmed Bakr Abdelwahab та Gilbert Kirsch. "Synthetic Routes to Coumarin(Benzopyrone)-Fused Five-Membered Aromatic Heterocycles Built on the α-Pyrone Moiety. Part II: Five-Membered Aromatic Rings with Multi Heteroatoms". Molecules 26, № 11 (4 червня 2021): 3409. http://dx.doi.org/10.3390/molecules26113409.
Повний текст джерелаKaur, Arvinder, Anju Goyal, Vishnu Nayak Badavath, Rajwinder Kaur, Sandeep Arora, and Ramninder Kaur. "Synthesis and Pharmacological Evaluation of Promising Coumarin Methyl Ester/ Di/Tri/Tetra Peptide Derivatives." ECS Transactions 107, no. 1 (April 24, 2022): 6747–61. http://dx.doi.org/10.1149/10701.6747ecst.
Повний текст джерелаWalki, Shashikanth, S. Naveen, S. Kenchanna, K. M. Mahadevan, M. N. Kumara, and N. K. Lokanath. "Crystal structure of 8-ethoxy-3-(4-nitrophenyl)-2H-chromen-2-one." Acta Crystallographica Section E Crystallographic Communications 71, no. 11 (October 17, 2015): o860—o861. http://dx.doi.org/10.1107/s2056989015019325.
Повний текст джерелаYang, Jian-Xin, Hong-Yan Liu, and Xiang-Hui Wang. "4-Methyl-2-oxo-2H-chromen-7-yl 4-methylbenzenesulfonate." Acta Crystallographica Section E Structure Reports Online 68, no. 4 (March 28, 2012): o1191. http://dx.doi.org/10.1107/s1600536812012238.
Повний текст джерелаDevarajegowda, H. C., P. A. Suchetan, S. Sreenivasa, H. T. Srinivasa, and B. S. Palakshamurthy. "Crystal structure of 4-methoxyphenyl 2-oxo-2H-chromene-3-carboxylate." Acta Crystallographica Section E Crystallographic Communications 71, no. 6 (May 7, 2015): o374—o375. http://dx.doi.org/10.1107/s2056989015006970.
Повний текст джерелаBauri, A. K., Sabine Foro, Hans-Jörg Lindner, and Sandip K. Nayak. "Reinvestigation of seselin." Acta Crystallographica Section E Structure Reports Online 62, no. 4 (March 10, 2006): o1340—o1341. http://dx.doi.org/10.1107/s1600536806008221.
Повний текст джерелаSreenivasa, S., H. T. Srinivasa, B. S. Palakshamurthy, Vijith Kumar, and H. C. Devarajegowda. "4′-Cyanobiphenyl-4-yl 7-diethylamino-2-oxo-2H-chromene-3-carboxylate." Acta Crystallographica Section E Structure Reports Online 69, no. 2 (January 19, 2013): o266. http://dx.doi.org/10.1107/s1600536813001591.
Повний текст джерелаGouda, Moustafa A., Mohammed A. Salem, and Mohamed H. Helal. "A Review on Synthesis and Pharmacological Activity of Coumarins and Their Analogs." Current Bioactive Compounds 16, no. 6 (October 2, 2020): 818–36. http://dx.doi.org/10.2174/1573407215666190405154406.
Повний текст джерелаSingh, Parvesh, Nomandla Ngcoya, Ramgopal Mopuri, Nagaraju Kerru, Neha Manhas, Oluwakemi Ebenezer та Md Shahidul Islam. "α-Glucosidase Inhibition, Antioxidant and Docking Studies of Hydroxycoumarins and their Mono and Bis O-alkylated/acetylated Analogs". Letters in Drug Design & Discovery 15, № 2 (30 січня 2018): 127–35. http://dx.doi.org/10.2174/1570180814666170602081941.
Повний текст джерелаChoudhury, Sudip, Satya Paul, K. Majumdar, and Siddique Anwar. "Copper(I) Iodide Supported Synthesis of Coumarin- and Quinolone-Annulated 2-Aminothiazoles." Synlett 26, no. 08 (March 3, 2015): 1039–44. http://dx.doi.org/10.1055/s-0034-1380272.
Повний текст джерелаSinha, Shweta, Kuldeep Singh, Akash Ved, Syed Misbahul Hasan, and Samar Mujeeb. "Therapeutic Journey and Recent Advances in the Synthesis of Coumarin Derivatives." Mini-Reviews in Medicinal Chemistry 22, no. 9 (May 2022): 1314–30. http://dx.doi.org/10.2174/1389557521666211116120823.
Повний текст джерелаdo Nascimento, Jainara Santos, João Carlos Silva Conceição, and Eliane de Oliveira Silva. "Biotransformation of Coumarins by Filamentous Fungi: An Alternative Way for Achievement of Bioactive Analogs." Mini-Reviews in Organic Chemistry 16, no. 6 (August 27, 2019): 568–77. http://dx.doi.org/10.2174/1570193x15666180803094216.
Повний текст джерелаKarataş, Mert Olgun, Bülent Alıcı, Vincenzo Passarelli, Ismail Özdemir, Jesús J. Pérez-Torrente, and Ricardo Castarlenas. "Iridium(i) complexes bearing hemilabile coumarin-functionalised N-heterocyclic carbene ligands with application as alkyne hydrosilylation catalysts." Dalton Transactions 50, no. 32 (2021): 11206–15. http://dx.doi.org/10.1039/d1dt01946e.
Повний текст джерелаPaul, Saurav, Bimal B. Chakraborty, Kuheli Deb, and Sudip Choudhury. "FUSED RING HETEROCYCLE FUNCTIONALIZED GOLD NANOPARTICLES: SYNTHESIS AND SELF-ASSEMBLY." Chemical Problems 21, no. 2 (2023): 188–96. http://dx.doi.org/10.32737/2221-8688-2023-2-188-196.
Повний текст джерелаLiu, Yun, Yong-Miao Shen, Zhe Li, and Jian-Hua Xu. "2,4-Diphenyl-2-(trimethylsilyloxy)-3-dihydro-2H,5H-pyrano[3,2-c][1]benzopyran-5-one." Acta Crystallographica Section E Structure Reports Online 62, no. 4 (March 15, 2006): o1397—o1398. http://dx.doi.org/10.1107/s1600536806009020.
Повний текст джерелаKothavale, Shantaram, and Nagaiyan Sekar. "A new type of triphenylamine based coumarin–rhodamine hybrid compound: synthesis, photophysical properties, viscosity sensitivity and energy transfer." RSC Advances 6, no. 107 (2016): 105387–97. http://dx.doi.org/10.1039/c6ra24485h.
Повний текст джерелаQuezada, Elías, Fernanda Rodríguez-Enríquez, Reyes Laguna, Elena Cutrín, Francisco Otero, Eugenio Uriarte, and Dolores Viña. "Curcumin–Coumarin Hybrid Analogues as Multitarget Agents in Neurodegenerative Disorders." Molecules 26, no. 15 (July 28, 2021): 4550. http://dx.doi.org/10.3390/molecules26154550.
Повний текст джерелаJournal, Baghdad Science. "Synthesis and Characterization of New Mannich Bases Derived from 7-hydroxy-4-methyl Coumarin." Baghdad Science Journal 13, no. 2 (June 5, 2016): 235–43. http://dx.doi.org/10.21123/bsj.13.2.235-243.
Повний текст джерелаShao, Jiaan, Wenteng Chen, Di Ke, Ke Shu, En Chen, and Yongping Yu. "Highly Efficient Synthesis of Polysubstituted 2-Aminopyrroles via a Multicomponent Domino Reaction." Synlett 29, no. 07 (February 15, 2018): 922–27. http://dx.doi.org/10.1055/s-0036-1591907.
Повний текст джерелаOuédraogo, Mohammad, Akoun Abou, Abdoulaye Djandé, Olivier Ouari, and T. Jérémie Zoueu. "2-Oxo-2H-chromen-7-yl 4-tert-butylbenzoate." Acta Crystallographica Section E Crystallographic Communications 74, no. 4 (March 16, 2018): 530–34. http://dx.doi.org/10.1107/s2056989018004188.
Повний текст джерелаAbou, Akoun, Jules Yoda, Abdoulaye Djandé, Stéphane Coussan, and T. Jérémie Zoueu. "Crystal structure of 2-oxo-2H-chromen-7-yl 4-fluorobenzoate." Acta Crystallographica Section E Crystallographic Communications 74, no. 5 (April 27, 2018): 761–65. http://dx.doi.org/10.1107/s205698901800614x.
Повний текст джерелаManojkumar, Parameswaran, Thengungal Ravi, and Gopalakrishnan Subbuchettiar. "Synthesis of coumarin heterocyclic derivatives with antioxidant activity and in vitro cytotoxic activity against tumour cells." Acta Pharmaceutica 59, no. 2 (June 1, 2009): 159–70. http://dx.doi.org/10.2478/v10007-009-0018-7.
Повний текст джерелаGomes, Lígia R., John Nicolson Low, André Fonseca, Maria João Matos, and Fernanda Borges. "6-Methyl-2-oxo-N-(quinolin-6-yl)-2H-chromene-3-carboxamide: crystal structure and Hirshfeld surface analysis." Acta Crystallographica Section E Crystallographic Communications 72, no. 8 (July 12, 2016): 1121–25. http://dx.doi.org/10.1107/s2056989016011026.
Повний текст джерелаZhang, Hengrui, and Zhijie Fang. "Design and Synthesis of Novel Vitamin D–Coumarin Hybrids using Microwave Irradiation." Journal of Chemical Research 41, no. 12 (December 2017): 684–87. http://dx.doi.org/10.3184/174751917x15121208772534.
Повний текст джерелаZhang, Kuan, Huabin Han, Lele Wang, Ziying Zhang, Qilin Wang, Wenjing Zhang, and Zhanwei Bu. "An unexpected cascade reaction of 3-hydroxyoxindoles with coumarin-3-carboxylates to construct 2,3-dihydrobenzofuran spirooxindoles." Chemical Communications 55, no. 91 (2019): 13681–84. http://dx.doi.org/10.1039/c9cc07114h.
Повний текст джерелаTran, Nguyen Khoi Song, Tuy An Trinh, Jaesung Pyo, Chang Geon Kim, Jae Gyu Park, and Ki Sung Kang. "Neuroprotective Potential of Pyranocoumarins from Angelica gigas Nakai on Glutamate-Induced Hippocampal Cell Death." Antioxidants 12, no. 8 (August 21, 2023): 1651. http://dx.doi.org/10.3390/antiox12081651.
Повний текст джерелаDouka, Matina D., and Konstantinos E. Litinas. "An Overview on the Synthesis of Fused Pyridocoumarins with Biological Interest." Molecules 27, no. 21 (October 26, 2022): 7256. http://dx.doi.org/10.3390/molecules27217256.
Повний текст джерелаKatopodi, Annita, Evangelia Tsotsou, Triantafylia Iliou, Georgia-Eirini Deligiannidou, Eleni Pontiki, Christos Kontogiorgis, Fotios Tsopelas, and Anastasia Detsi. "Synthesis, Bioactivity, Pharmacokinetic and Biomimetic Properties of Multi-Substituted Coumarin Derivatives." Molecules 26, no. 19 (October 2, 2021): 5999. http://dx.doi.org/10.3390/molecules26195999.
Повний текст джерелаJustus, Eugen, Dana T. Izteleuova, Alexander V. Kasantsev, Mendel M. Axartov, Enno Lork, and Detlef Gabel. "Preparation of Carboranyl and Dodecaborate Derivatives of Coumarin." Collection of Czechoslovak Chemical Communications 72, no. 12 (2007): 1740–54. http://dx.doi.org/10.1135/cccc20071740.
Повний текст джерелаPoronik, Yevgen M., and Daniel T. Gryko. "Pentacyclic coumarin-based blue emitters – the case of bifunctional nucleophilic behavior of amidines." Chem. Commun. 50, no. 43 (2014): 5688–90. http://dx.doi.org/10.1039/c4cc01106f.
Повний текст джерелаPujar, Kiran K., Manohar V. Kulkarni, and G. N. Anil Kumar. "Crystal structure of 6,6′-dimethyl-2H,2′H-3,4′-bichromene-2,2′-dione." Acta Crystallographica Section E Structure Reports Online 70, no. 11 (October 11, 2014): 319–21. http://dx.doi.org/10.1107/s1600536814021825.
Повний текст джерелаSun, Zhiyuan, Yu Wang, De-Cai Fang, and Yuxia Zhao. "The effects of bromine atoms on the photophysical and photochemical properties of 3-cinnamoylcoumarin derivatives." New Journal of Chemistry 42, no. 9 (2018): 7377–82. http://dx.doi.org/10.1039/c8nj00966j.
Повний текст джерелаChai, Lan-Qin, Hong-Song Zhang, Yu-Li Zhang, and Kai Cui. "Synthesis of Asymmetric Semicarbazides using a Coumarin Ring." Journal of Chemical Research 36, no. 1 (January 2012): 12–14. http://dx.doi.org/10.3184/174751912x13249848731931.
Повний текст джерелаTlenkopatchev, Mikhail A., Serguei Fomine, Lioudmila Fomina, Ruben Gaviño, and Takeshi Ogawa. "Ring-Opening Metathesis Polymerization of Coumarin-Containing Norbornene." Polymer Journal 29, no. 7 (July 1997): 622–25. http://dx.doi.org/10.1295/polymj.29.622.
Повний текст джерелаFang, Mingxi, Rashmi Adhikari, Jianheng Bi, Wafa Mazi, Nethaniah Dorh, Jianbo Wang, Nathan Conner, et al. "Fluorescent probes for sensitive and selective detection of pH changes in live cells in visible and near-infrared channels." Journal of Materials Chemistry B 5, no. 48 (2017): 9579–90. http://dx.doi.org/10.1039/c7tb02583a.
Повний текст джерелаMurdock, Daniel, Rebecca A. Ingle, Igor V. Sazanovich, Ian P. Clark, Yu Harabuchi, Tetsuya Taketsugu, Satoshi Maeda, Andrew J. Orr-Ewing та Michael N. R. Ashfold. "Contrasting ring-opening propensities in UV-excited α-pyrone and coumarin". Physical Chemistry Chemical Physics 18, № 4 (2016): 2629–38. http://dx.doi.org/10.1039/c5cp06597f.
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