Artículos de revistas sobre el tema "Coumarin ring"
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Prahadeesh, N., Maheswaran Sithambaresan y Umaramani Mathiventhan. "A Study on Hydrogen Peroxide Scavenging Activity and Ferric Reducing Ability of Simple Coumarins". Emerging Science Journal 2, n.º 6 (13 de diciembre de 2018): 417. http://dx.doi.org/10.28991/esj-2018-01161.
Texto completoMohan, Resmi, M. Vidhyalakshmi y Venkatasubramanian Sivakumar. "Microwave Assisted Rapid Extraction and Characterization of Coumarin from Fig Plant (Ficus carica)". Asian Journal of Science and Applied Technology 8, n.º 1 (5 de mayo de 2019): 1–4. http://dx.doi.org/10.51983/ajsat-2019.8.1.1043.
Texto completoYoon, Jeong A. y 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, n.º 24 (30 de septiembre de 2019): 4611–18. http://dx.doi.org/10.1055/s-0037-1610730.
Texto completoKumari, Sumita, Amit Sharma y Sonia Yadav. "Pharmacological Potential of Coumarin-Based Derivatives: (A Comprehensive Brief Review)". Oriental Journal Of Chemistry 39, n.º 3 (30 de junio de 2023): 568–76. http://dx.doi.org/10.13005/ojc/390304.
Texto completoMedyouni, Rawdha, Olfa Naouali, Naceur HAMDI y Lassaad Baklouti. "Coumarin phthalonitriles: Synthesis and cation binding properties". JOURNAL OF ADVANCES IN CHEMISTRY 11, n.º 4 (9 de marzo de 2015): 3512–18. http://dx.doi.org/10.24297/jac.v11i4.6695.
Texto completoCheke, 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, n.º 5 (24 de abril de 2022): 566. http://dx.doi.org/10.3390/antibiotics11050566.
Texto completoThakur, Abhinay, Rohit Sharma, Vivek Sheel Jaswal, Eugenie Nepovimova, Ashun Chaudhary y Kamil Kuca. "Psoralen: A Biologically Important Coumarin with Emerging Applications". Mini-Reviews in Medicinal Chemistry 20, n.º 18 (7 de diciembre de 2020): 1838–45. http://dx.doi.org/10.2174/1389557520666200429101053.
Texto completoJalhan, Sunny. "Review Article: Various Biological Activities of Coumarin and Oxadiazole Derivatives." Asian Journal of Pharmaceutical and Clinical Research 10, n.º 7 (1 de julio de 2017): 38. http://dx.doi.org/10.22159/ajpcr.2017.v10i7.18461.
Texto completoSanaryh Mohammed Al-awad, Leaqaa Abdalredha raheem y Ausama Ayob Jaccob. "Synthesis and Pharmacological Evaluation of Novel Coumarin Derivatives". International Journal of Research in Pharmaceutical Sciences 11, n.º 1 (27 de enero de 2020): 865–74. http://dx.doi.org/10.26452/ijrps.v11i1.1908.
Texto completoZeydi, Masoud Mohammadi, Seyed Jafar Kalantarian y Zahra Kazeminejad. "Overview on developed synthesis procedures of coumarin heterocycles". Journal of the Iranian Chemical Society 17, n.º 12 (27 de junio de 2020): 3031–94. http://dx.doi.org/10.1007/s13738-020-01984-1.
Texto completoSouza, Simone M. de, Franco Delle Monache y Artur Smânia. "Antibacterial Activity of Coumarins". Zeitschrift für Naturforschung C 60, n.º 9-10 (1 de octubre de 2005): 693–700. http://dx.doi.org/10.1515/znc-2005-9-1006.
Texto completoOlyaei, Abolfazl, Mahnaz Saraei y Reyhaneh Khoeiniha. "Catalyst-Free One-Pot Synthesis of Novel Heteroarylamine Substituted Furo[3,2-c]coumarins". Synlett 29, n.º 12 (17 de mayo de 2018): 1589–92. http://dx.doi.org/10.1055/s-0036-1591582.
Texto completoShahi, Akbar Massoumi, Mohammad Nikpassand y 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, n.º 8 (28 de octubre de 2020): 648–53. http://dx.doi.org/10.2174/1570179417666200520111536.
Texto completoZhou, Li-Ping y 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, n.º 2 (22 de enero de 2014): o176. http://dx.doi.org/10.1107/s1600536814001123.
Texto completoEl-Sawy, Eslam Reda, Ahmed Bakr Abdelwahab y 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, n.º 11 (4 de junio de 2021): 3409. http://dx.doi.org/10.3390/molecules26113409.
Texto completoKaur, Arvinder, Anju Goyal, Vishnu Nayak Badavath, Rajwinder Kaur, Sandeep Arora y Ramninder Kaur. "Synthesis and Pharmacological Evaluation of Promising Coumarin Methyl Ester/ Di/Tri/Tetra Peptide Derivatives". ECS Transactions 107, n.º 1 (24 de abril de 2022): 6747–61. http://dx.doi.org/10.1149/10701.6747ecst.
Texto completoWalki, Shashikanth, S. Naveen, S. Kenchanna, K. M. Mahadevan, M. N. Kumara y N. K. Lokanath. "Crystal structure of 8-ethoxy-3-(4-nitrophenyl)-2H-chromen-2-one". Acta Crystallographica Section E Crystallographic Communications 71, n.º 11 (17 de octubre de 2015): o860—o861. http://dx.doi.org/10.1107/s2056989015019325.
Texto completoYang, Jian-Xin, Hong-Yan Liu y Xiang-Hui Wang. "4-Methyl-2-oxo-2H-chromen-7-yl 4-methylbenzenesulfonate". Acta Crystallographica Section E Structure Reports Online 68, n.º 4 (28 de marzo de 2012): o1191. http://dx.doi.org/10.1107/s1600536812012238.
Texto completoDevarajegowda, H. C., P. A. Suchetan, S. Sreenivasa, H. T. Srinivasa y B. S. Palakshamurthy. "Crystal structure of 4-methoxyphenyl 2-oxo-2H-chromene-3-carboxylate". Acta Crystallographica Section E Crystallographic Communications 71, n.º 6 (7 de mayo de 2015): o374—o375. http://dx.doi.org/10.1107/s2056989015006970.
Texto completoBauri, A. K., Sabine Foro, Hans-Jörg Lindner y Sandip K. Nayak. "Reinvestigation of seselin". Acta Crystallographica Section E Structure Reports Online 62, n.º 4 (10 de marzo de 2006): o1340—o1341. http://dx.doi.org/10.1107/s1600536806008221.
Texto completoSreenivasa, S., H. T. Srinivasa, B. S. Palakshamurthy, Vijith Kumar y H. C. Devarajegowda. "4′-Cyanobiphenyl-4-yl 7-diethylamino-2-oxo-2H-chromene-3-carboxylate". Acta Crystallographica Section E Structure Reports Online 69, n.º 2 (19 de enero de 2013): o266. http://dx.doi.org/10.1107/s1600536813001591.
Texto completoGouda, Moustafa A., Mohammed A. Salem y Mohamed H. Helal. "A Review on Synthesis and Pharmacological Activity of Coumarins and Their Analogs". Current Bioactive Compounds 16, n.º 6 (2 de octubre de 2020): 818–36. http://dx.doi.org/10.2174/1573407215666190405154406.
Texto completoSingh, Parvesh, Nomandla Ngcoya, Ramgopal Mopuri, Nagaraju Kerru, Neha Manhas, Oluwakemi Ebenezer y 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, n.º 2 (30 de enero de 2018): 127–35. http://dx.doi.org/10.2174/1570180814666170602081941.
Texto completoChoudhury, Sudip, Satya Paul, K. Majumdar y Siddique Anwar. "Copper(I) Iodide Supported Synthesis of Coumarin- and Quinolone-Annulated 2-Aminothiazoles". Synlett 26, n.º 08 (3 de marzo de 2015): 1039–44. http://dx.doi.org/10.1055/s-0034-1380272.
Texto completoSinha, Shweta, Kuldeep Singh, Akash Ved, Syed Misbahul Hasan y Samar Mujeeb. "Therapeutic Journey and Recent Advances in the Synthesis of Coumarin Derivatives". Mini-Reviews in Medicinal Chemistry 22, n.º 9 (mayo de 2022): 1314–30. http://dx.doi.org/10.2174/1389557521666211116120823.
Texto completodo Nascimento, Jainara Santos, João Carlos Silva Conceição y Eliane de Oliveira Silva. "Biotransformation of Coumarins by Filamentous Fungi: An Alternative Way for Achievement of Bioactive Analogs". Mini-Reviews in Organic Chemistry 16, n.º 6 (27 de agosto de 2019): 568–77. http://dx.doi.org/10.2174/1570193x15666180803094216.
Texto completoKarataş, Mert Olgun, Bülent Alıcı, Vincenzo Passarelli, Ismail Özdemir, Jesús J. Pérez-Torrente y Ricardo Castarlenas. "Iridium(i) complexes bearing hemilabile coumarin-functionalised N-heterocyclic carbene ligands with application as alkyne hydrosilylation catalysts". Dalton Transactions 50, n.º 32 (2021): 11206–15. http://dx.doi.org/10.1039/d1dt01946e.
Texto completoPaul, Saurav, Bimal B. Chakraborty, Kuheli Deb y Sudip Choudhury. "FUSED RING HETEROCYCLE FUNCTIONALIZED GOLD NANOPARTICLES: SYNTHESIS AND SELF-ASSEMBLY". Chemical Problems 21, n.º 2 (2023): 188–96. http://dx.doi.org/10.32737/2221-8688-2023-2-188-196.
Texto completoLiu, Yun, Yong-Miao Shen, Zhe Li y 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, n.º 4 (15 de marzo de 2006): o1397—o1398. http://dx.doi.org/10.1107/s1600536806009020.
Texto completoKothavale, Shantaram y Nagaiyan Sekar. "A new type of triphenylamine based coumarin–rhodamine hybrid compound: synthesis, photophysical properties, viscosity sensitivity and energy transfer". RSC Advances 6, n.º 107 (2016): 105387–97. http://dx.doi.org/10.1039/c6ra24485h.
Texto completoQuezada, Elías, Fernanda Rodríguez-Enríquez, Reyes Laguna, Elena Cutrín, Francisco Otero, Eugenio Uriarte y Dolores Viña. "Curcumin–Coumarin Hybrid Analogues as Multitarget Agents in Neurodegenerative Disorders". Molecules 26, n.º 15 (28 de julio de 2021): 4550. http://dx.doi.org/10.3390/molecules26154550.
Texto completoJournal, Baghdad Science. "Synthesis and Characterization of New Mannich Bases Derived from 7-hydroxy-4-methyl Coumarin". Baghdad Science Journal 13, n.º 2 (5 de junio de 2016): 235–43. http://dx.doi.org/10.21123/bsj.13.2.235-243.
Texto completoShao, Jiaan, Wenteng Chen, Di Ke, Ke Shu, En Chen y Yongping Yu. "Highly Efficient Synthesis of Polysubstituted 2-Aminopyrroles via a Multicomponent Domino Reaction". Synlett 29, n.º 07 (15 de febrero de 2018): 922–27. http://dx.doi.org/10.1055/s-0036-1591907.
Texto completoOuédraogo, Mohammad, Akoun Abou, Abdoulaye Djandé, Olivier Ouari y T. Jérémie Zoueu. "2-Oxo-2H-chromen-7-yl 4-tert-butylbenzoate". Acta Crystallographica Section E Crystallographic Communications 74, n.º 4 (16 de marzo de 2018): 530–34. http://dx.doi.org/10.1107/s2056989018004188.
Texto completoAbou, Akoun, Jules Yoda, Abdoulaye Djandé, Stéphane Coussan y T. Jérémie Zoueu. "Crystal structure of 2-oxo-2H-chromen-7-yl 4-fluorobenzoate". Acta Crystallographica Section E Crystallographic Communications 74, n.º 5 (27 de abril de 2018): 761–65. http://dx.doi.org/10.1107/s205698901800614x.
Texto completoManojkumar, Parameswaran, Thengungal Ravi y Gopalakrishnan Subbuchettiar. "Synthesis of coumarin heterocyclic derivatives with antioxidant activity and in vitro cytotoxic activity against tumour cells". Acta Pharmaceutica 59, n.º 2 (1 de junio de 2009): 159–70. http://dx.doi.org/10.2478/v10007-009-0018-7.
Texto completoGomes, Lígia R., John Nicolson Low, André Fonseca, Maria João Matos y 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, n.º 8 (12 de julio de 2016): 1121–25. http://dx.doi.org/10.1107/s2056989016011026.
Texto completoZhang, Hengrui y Zhijie Fang. "Design and Synthesis of Novel Vitamin D–Coumarin Hybrids using Microwave Irradiation". Journal of Chemical Research 41, n.º 12 (diciembre de 2017): 684–87. http://dx.doi.org/10.3184/174751917x15121208772534.
Texto completoZhang, Kuan, Huabin Han, Lele Wang, Ziying Zhang, Qilin Wang, Wenjing Zhang y Zhanwei Bu. "An unexpected cascade reaction of 3-hydroxyoxindoles with coumarin-3-carboxylates to construct 2,3-dihydrobenzofuran spirooxindoles". Chemical Communications 55, n.º 91 (2019): 13681–84. http://dx.doi.org/10.1039/c9cc07114h.
Texto completoTran, Nguyen Khoi Song, Tuy An Trinh, Jaesung Pyo, Chang Geon Kim, Jae Gyu Park y Ki Sung Kang. "Neuroprotective Potential of Pyranocoumarins from Angelica gigas Nakai on Glutamate-Induced Hippocampal Cell Death". Antioxidants 12, n.º 8 (21 de agosto de 2023): 1651. http://dx.doi.org/10.3390/antiox12081651.
Texto completoDouka, Matina D. y Konstantinos E. Litinas. "An Overview on the Synthesis of Fused Pyridocoumarins with Biological Interest". Molecules 27, n.º 21 (26 de octubre de 2022): 7256. http://dx.doi.org/10.3390/molecules27217256.
Texto completoKatopodi, Annita, Evangelia Tsotsou, Triantafylia Iliou, Georgia-Eirini Deligiannidou, Eleni Pontiki, Christos Kontogiorgis, Fotios Tsopelas y Anastasia Detsi. "Synthesis, Bioactivity, Pharmacokinetic and Biomimetic Properties of Multi-Substituted Coumarin Derivatives". Molecules 26, n.º 19 (2 de octubre de 2021): 5999. http://dx.doi.org/10.3390/molecules26195999.
Texto completoJustus, Eugen, Dana T. Izteleuova, Alexander V. Kasantsev, Mendel M. Axartov, Enno Lork y Detlef Gabel. "Preparation of Carboranyl and Dodecaborate Derivatives of Coumarin". Collection of Czechoslovak Chemical Communications 72, n.º 12 (2007): 1740–54. http://dx.doi.org/10.1135/cccc20071740.
Texto completoPoronik, Yevgen M. y Daniel T. Gryko. "Pentacyclic coumarin-based blue emitters – the case of bifunctional nucleophilic behavior of amidines". Chem. Commun. 50, n.º 43 (2014): 5688–90. http://dx.doi.org/10.1039/c4cc01106f.
Texto completoPujar, Kiran K., Manohar V. Kulkarni y 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, n.º 11 (11 de octubre de 2014): 319–21. http://dx.doi.org/10.1107/s1600536814021825.
Texto completoSun, Zhiyuan, Yu Wang, De-Cai Fang y Yuxia Zhao. "The effects of bromine atoms on the photophysical and photochemical properties of 3-cinnamoylcoumarin derivatives". New Journal of Chemistry 42, n.º 9 (2018): 7377–82. http://dx.doi.org/10.1039/c8nj00966j.
Texto completoChai, Lan-Qin, Hong-Song Zhang, Yu-Li Zhang y Kai Cui. "Synthesis of Asymmetric Semicarbazides using a Coumarin Ring". Journal of Chemical Research 36, n.º 1 (enero de 2012): 12–14. http://dx.doi.org/10.3184/174751912x13249848731931.
Texto completoTlenkopatchev, Mikhail A., Serguei Fomine, Lioudmila Fomina, Ruben Gaviño y Takeshi Ogawa. "Ring-Opening Metathesis Polymerization of Coumarin-Containing Norbornene". Polymer Journal 29, n.º 7 (julio de 1997): 622–25. http://dx.doi.org/10.1295/polymj.29.622.
Texto completoFang, 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, n.º 48 (2017): 9579–90. http://dx.doi.org/10.1039/c7tb02583a.
Texto completoMurdock, Daniel, Rebecca A. Ingle, Igor V. Sazanovich, Ian P. Clark, Yu Harabuchi, Tetsuya Taketsugu, Satoshi Maeda, Andrew J. Orr-Ewing y Michael N. R. Ashfold. "Contrasting ring-opening propensities in UV-excited α-pyrone and coumarin". Physical Chemistry Chemical Physics 18, n.º 4 (2016): 2629–38. http://dx.doi.org/10.1039/c5cp06597f.
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