Artículos de revistas sobre el tema "Heterocycles"
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Zhu, Yannan y You Huang. "Organocatalyzed [3+3] Annulations for the Construction of Heterocycles". Synthesis 52, n.º 08 (5 de febrero de 2020): 1181–202. http://dx.doi.org/10.1055/s-0039-1690810.
Texto completoAndres, C. J., Derek J. Denhart, Milind S. Deshpande y Kevin W. Gillman. "Recent Advances in the Solid Phase Synthesis of Drug Heterocyclic Small Molecules". Combinatorial Chemistry & High Throughput Screening 2, n.º 4 (agosto de 1999): 191–210. http://dx.doi.org/10.2174/1386207302666220204193145.
Texto completoLuna, Isadora Silva, Rayssa Marques Duarte da Cruz, Ryldene Marques Duarte da Cruz, Rodrigo Santos Aquino de Araújo y Francisco Jaime Bezerra Mendonça-Junior. "1,4-Dithiane-2,5-diol: A Versatile Synthon for the Synthesis of Sulfur-containing Heterocycles". Current Organic Synthesis 15, n.º 8 (17 de diciembre de 2018): 1026–42. http://dx.doi.org/10.2174/1570179415666180821154551.
Texto completoWinne, Johan, Jan Hullaert, Bram Denoo, Mien Christiaens y Brenda Callebaut. "Heterocycles as Moderators of Allyl Cation Cycloaddition Reactivity". Synlett 28, n.º 18 (27 de julio de 2017): 2345–52. http://dx.doi.org/10.1055/s-0036-1588511.
Texto completoRusu, Aura, Ioana-Maria Moga, Livia Uncu y Gabriel Hancu. "The Role of Five-Membered Heterocycles in the Molecular Structure of Antibacterial Drugs Used in Therapy". Pharmaceutics 15, n.º 11 (29 de octubre de 2023): 2554. http://dx.doi.org/10.3390/pharmaceutics15112554.
Texto completoSlivka, Mikhailo y Mikhailo Onysko. "The Use of Electrophilic Cyclization for the Preparation of Condensed Heterocycles". Synthesis 53, n.º 19 (19 de mayo de 2021): 3497–512. http://dx.doi.org/10.1055/s-0040-1706036.
Texto completoCui, Hai-Lei. "Recent Advances in DMSO-Based Direct Synthesis of Heterocycles". Molecules 27, n.º 23 (2 de diciembre de 2022): 8480. http://dx.doi.org/10.3390/molecules27238480.
Texto completoĀbele, E., R. Ābele, Ļ. Golomba, J. Višņevska, T. Beresņeva y K. Rubina. "Oximes of Seven-Membered Heterocyclic Compounds Containing One Heteroatom". Latvian Journal of Chemistry 50, n.º 3-4 (1 de enero de 2011): 205–22. http://dx.doi.org/10.2478/v10161-011-0071-7.
Texto completoLechel, Tilman y Hans-Ulrich Reissig. "Synthesis of heterocycles via alkoxyallenes". Pure and Applied Chemistry 82, n.º 9 (31 de mayo de 2010): 1835–44. http://dx.doi.org/10.1351/pac-con-09-09-06.
Texto completoĀbele, E. "Oximes of Seven-Membered Heterocyclic Compounds Containing Two Heteroatoms". Latvian Journal of Chemistry 51, n.º 1-2 (1 de enero de 2012): 83–92. http://dx.doi.org/10.2478/v10161-012-0005-z.
Texto completoEgbujor, Melford C., Paolo Tucci, Ugomma C. Onyeije, Chigbundu N. Emeruwa y Luciano Saso. "NRF2 Activation by Nitrogen Heterocycles: A Review". Molecules 28, n.º 6 (18 de marzo de 2023): 2751. http://dx.doi.org/10.3390/molecules28062751.
Texto completoYadav, Shailendra, Sushma Singh y Chitrasen Gupta. "A CONCISE OVERVIEW ON HETEROCYCLIC COMPOUNDS EXHIBITING PESTICIDAL ACTIVITIES". International Journal of Advanced Research 9, n.º 08 (31 de agosto de 2021): 989–1004. http://dx.doi.org/10.21474/ijar01/13352.
Texto completoShaikh, Ansar R., Mazahar Farooqui, R. H. Satpute y Syed Abed. "Overview on Nitrogen containing compounds and their assessment based on ‘International Regulatory Standards’". Journal of Drug Delivery and Therapeutics 8, n.º 6-s (21 de diciembre de 2018): 424–28. http://dx.doi.org/10.22270/jddt.v8i6-s.2156.
Texto completoMaji, Pradip Kumar. "Recent Progress in the Synthesis of Pyrimidine Heterocycles: A Review". Current Organic Chemistry 24, n.º 10 (11 de agosto de 2020): 1055–96. http://dx.doi.org/10.2174/1385272824999200507123843.
Texto completoDudhe, Anshu R., Sachinkumar D. Gunjal, Sampath AG, Sushama Rawat y YY Nandurkar. "An Overview on Nitrogen-containing Heterocyclic Compounds as Anticancer Agents". INTERNATIONAL JOURNAL OF PHARMACEUTICAL QUALITY ASSURANCE 14, n.º 04 (25 de diciembre de 2023): 1296–301. http://dx.doi.org/10.25258/ijpqa.14.4.72.
Texto completoNiedballa, Jonas y Thomas J. J. Müller. "Heterocycles by Consecutive Multicomponent Syntheses via Catalytically Generated Alkynoyl Intermediates". Catalysts 12, n.º 1 (13 de enero de 2022): 90. http://dx.doi.org/10.3390/catal12010090.
Texto completoDrapak, І. V. "In silico screening of drug-like molecules for the treatment of cardiovascular diseases on the basis of five-membered privileged heterocycles". Farmatsevtychnyi zhurnal, n.º 4 (10 de septiembre de 2019): 61–72. http://dx.doi.org/10.32352/0367-3057.4.19.07.
Texto completoSparr, Christof y Christian Fischer. "Configurationally Stable Atropisomeric Acridinium Fluorophores". Synlett 29, n.º 16 (3 de agosto de 2018): 2176–80. http://dx.doi.org/10.1055/s-0037-1610233.
Texto completoBirzan, Liviu, Mihaela Cristea, Constantin C. Draghici y Alexandru C. Razus. "Some Considerations Regarding the 1H and 13C Spectra of 4-(1-azulenyl)-2,6-bis(2-heteroaryl-vinyl)- pyrylium and Pyridinium and their Corresponding Pyridines". Revista de Chimie 69, n.º 1 (15 de febrero de 2018): 64–69. http://dx.doi.org/10.37358/rc.18.1.6045.
Texto completoLi, Jin-Heng, De-Lie An y Jing-Hao Qin. "Recent Advances in Cycloaddition Reactions with Alkynes to Construct Heterocycles". Synthesis 52, n.º 24 (13 de octubre de 2020): 3818–36. http://dx.doi.org/10.1055/s-0040-1707355.
Texto completoMoulis, Pierre, Cécile Miot-Sertier, Laure Cordazzo, Olivier Claisse, Céline Franc, Laurent Riquier, Warren Albertin et al. "Which microorganisms contribute to mousy off-flavour in our wines?" OENO One 57, n.º 2 (16 de mayo de 2023): 177–87. http://dx.doi.org/10.20870/oeno-one.2023.57.2.7481.
Texto completoAdak, Laksmikanta y Tubai Ghosh. "Recent Progress in Iron-Catalyzed Reactions Towards the Synthesis of Bioactive Five- and Six-Membered Heterocycles". Current Organic Chemistry 24, n.º 22 (18 de diciembre de 2020): 2634–64. http://dx.doi.org/10.2174/1385272824999200714102103.
Texto completoHoffman, Gavin R. y Allen M. Schoffstall. "Syntheses and Applications of 1,2,3-Triazole-Fused Pyrazines and Pyridazines". Molecules 27, n.º 15 (22 de julio de 2022): 4681. http://dx.doi.org/10.3390/molecules27154681.
Texto completoKerru, Nagaraju, Lalitha Gummidi, Suresh Maddila, Kranthi Kumar Gangu y Sreekantha B. Jonnalagadda. "A Review on Recent Advances in Nitrogen-Containing Molecules and Their Biological Applications". Molecules 25, n.º 8 (20 de abril de 2020): 1909. http://dx.doi.org/10.3390/molecules25081909.
Texto completoKumar, Adarsh, Ankit Kumar Singh, Harshwardhan Singh, Veena Vijayan, Deepak Kumar, Jashwanth Naik, Suresh Thareja et al. "Nitrogen Containing Heterocycles as Anticancer Agents: A Medicinal Chemistry Perspective". Pharmaceuticals 16, n.º 2 (14 de febrero de 2023): 299. http://dx.doi.org/10.3390/ph16020299.
Texto completoNayl, AbdElAziz A., Ashraf A. Aly, Wael A. A. Arafa, Ismail M. Ahmed, Ahmed I. Abd-Elhamid, Esmail M. El-Fakharany, Mohamed A. Abdelgawad, Hendawy N. Tawfeek y Stefan Bräse. "Azides in the Synthesis of Various Heterocycles". Molecules 27, n.º 12 (9 de junio de 2022): 3716. http://dx.doi.org/10.3390/molecules27123716.
Texto completoXia, Xiao-Feng y Yan-Ning Niu. "Recent developments in the synthesis of nitrogen-containing heterocycles from β-aminovinyl esters/ketones as CC–N donors". Organic & Biomolecular Chemistry 20, n.º 2 (2022): 282–95. http://dx.doi.org/10.1039/d1ob01998h.
Texto completoKaur, Navjeet. "Metal and Non-Metal Catalysts in the Synthesis of Five-Membered S-Heterocycles". Current Organic Synthesis 16, n.º 2 (26 de marzo de 2019): 258–75. http://dx.doi.org/10.2174/1570179416666181207144430.
Texto completoMunzeiwa, Wisdom A., Bernard Omondi y Vincent O. Nyamori. "Architecture and synthesis of P,N-heterocyclic phosphine ligands". Beilstein Journal of Organic Chemistry 16 (12 de marzo de 2020): 362–83. http://dx.doi.org/10.3762/bjoc.16.35.
Texto completoGeisenberger, Josef, Jürgen Erbe, Jürgen Heidrich, Ulrich Nagela y Wolfgang Beck. "Pseudohalogenometallverbindungen, LXV [1] Synthese von Tetrazolen und Triazolen über die 1,3-dipolare Cycloaddition an die Azid-Liganden von polymeren Cobalt(III)-und Palladium(II)-Komplexen. Darstellung und Struktur von 5-TrichlormethyItetrazol / Pseudohalogeno Metal Compounds, LXV [1] Synthesis of Tetrazoles and Triazoles via 1,3-Dipolar Cycloaddition to the Azido Ligands of Polymerie Cobalt(III) and Palladium(II) Complexes. Synthesis and Structure of 5-Trichloromethyltetrazole". Zeitschrift für Naturforschung B 42, n.º 1 (1 de enero de 1987): 55–64. http://dx.doi.org/10.1515/znb-1987-0112.
Texto completoMaciejewski, Andrzej, Anna Jaworska-Augustyniak, Dariusz Radocki, Ronald G. Sutherland y Adam Piórko. "An efficient photochemical formation of phenoxazine and phenothiazine from their respective cyclopentadienyliron complexes". Collection of Czechoslovak Chemical Communications 54, n.º 8 (1989): 2171–75. http://dx.doi.org/10.1135/cccc19892171.
Texto completoPerlmutter, Patrick. "The Nucleophilic Addition/Eiectrophilic Ring Closure Route to Bio-Active Heterocycles". Current Medicinal Chemistry 3, n.º 2 (abril de 1996): 139–52. http://dx.doi.org/10.2174/092986730302220302101738.
Texto completoZhu, Daqian, Zhouming Wu, Liyun Liang, Yameng Sun, Bingling Luo, Peng Huang y Shijun Wen. "Heterocyclic iodoniums as versatile synthons to approach diversified polycyclic heteroarenes". RSC Advances 9, n.º 57 (2019): 33170–79. http://dx.doi.org/10.1039/c9ra07288h.
Texto completoMohareb, Rafat y Hanaa Hana. "Synthesis of progesterone heterocyclic derivatives of potential antimicrobial activity". Acta Pharmaceutica 58, n.º 1 (1 de marzo de 2008): 29–42. http://dx.doi.org/10.2478/v10007-007-0043-3.
Texto completoGroso, Emilia y Corinna Schindler. "Recent Advances in the Application of Ring-Closing Metathesis for the Synthesis of Unsaturated Nitrogen Heterocycles". Synthesis 51, n.º 05 (8 de febrero de 2019): 1100–1114. http://dx.doi.org/10.1055/s-0037-1611651.
Texto completoBreitwieser, Kevin y Peter Chen. "Crystal structure of a 1,1-dibutyl-1H,3H-naphtho[1,8-cd][1,2,6]oxastannaborinin-3-ol". Acta Crystallographica Section E Crystallographic Communications 77, n.º 2 (26 de enero de 2021): 180–83. http://dx.doi.org/10.1107/s2056989021000712.
Texto completoHuang, Pengfei, Pan Wang, Shengchun Wang, Shan Tang y Aiwen Lei. "Electrochemical oxidative [4 + 2] annulation of tertiary anilines and alkenes for the synthesis of tetrahydroquinolines". Green Chemistry 20, n.º 21 (2018): 4870–74. http://dx.doi.org/10.1039/c8gc02463d.
Texto completoBoelke, Andreas, Soleicha Sadat, Enno Lork y Boris J. Nachtsheim. "Pseudocyclic bis-N-heterocycle-stabilized iodanes – synthesis, characterization and applications". Chemical Communications 57, n.º 60 (2021): 7434–37. http://dx.doi.org/10.1039/d1cc03097c.
Texto completoLi, Xianwei, Tianzhang Wang, Yu-Jing Lu, Shaomin Ji, Yanping Huo y Bifu Liu. "Copper-catalyzed oxidative multicomponent reaction: synthesis of imidazo fused heterocycles with molecular oxygen". Organic & Biomolecular Chemistry 16, n.º 39 (2018): 7143–51. http://dx.doi.org/10.1039/c8ob01532e.
Texto completoAbbas, Sumayah Saadi, Azhar Mahdi Jasim, Tayseer Hamid Shakir y Iman Saadi Abbas. "Anticancer Activities of Some Heterocyclic Compounds Containing an Oxygen Atom: A Review". Al-Rafidain Journal of Medical Sciences ( ISSN: 2789-3219 ) 4 (27 de abril de 2023): 60–67. http://dx.doi.org/10.54133/ajms.v4i.109.
Texto completoMir, Reyaz Hassan, Roohi Mohi-ud-din, Taha Umair Wani, Mohammad Ovais Dar, Abdul Jaleel Shah, Bashir Lone, Chawla Pooja y Mubashir Hussain Masoodi. "Indole: A Privileged Heterocyclic Moiety in the Management of Cancer". Current Organic Chemistry 25, n.º 6 (26 de marzo de 2021): 724–36. http://dx.doi.org/10.2174/1385272825666210208142108.
Texto completoStephens, David E., Johant Lakey-Beitia, Jessica E. Burch, Hadi D. Arman y Oleg V. Larionov. "Mechanistic insights into the potassium tert-butoxide-mediated synthesis of N-heterobiaryls". Chemical Communications 52, n.º 64 (2016): 9945–48. http://dx.doi.org/10.1039/c6cc04816a.
Texto completoLi, Wen, Jinyang Zhang, Min Wang, Ru Dong, Xin Zhou, Xin Zheng y Liping Sun. "Pyrimidine-fused Dinitrogenous Penta-heterocycles as a Privileged Scaffold for Anti-Cancer Drug Discovery". Current Topics in Medicinal Chemistry 22, n.º 4 (febrero de 2022): 284–304. http://dx.doi.org/10.2174/1568026622666220111143949.
Texto completoKinjo, Rei y Bochao Su. "Construction of Boron-Containing Aromatic Heterocycles". Synthesis 49, n.º 14 (6 de junio de 2017): 2985–3034. http://dx.doi.org/10.1055/s-0036-1588832.
Texto completoZhang, Ming, Qiuhong Wang, Yiyuan Peng, Zhiyuan Chen, Changfeng Wan, Junmin Chen, Yongli Zhao, Rongli Zhang y Ai Qin Zhang. "Transition metal-catalyzed sp3 C–H activation and intramolecular C–N coupling to construct nitrogen heterocyclic scaffolds". Chemical Communications 55, n.º 87 (2019): 13048–65. http://dx.doi.org/10.1039/c9cc06609h.
Texto completoGonzález-González, Carlos A., Juan Javier Mejía Vega, Ricardo García Monroy, Davir González-Calderón, David Corona-Becerril, Aydeé Fuentes-Benítes, Joaquín Tamariz Mascarúa y Carlos González-Romero. "A Novel and Chemoselective Process ofN-Alkylation of Aromatic Nitrogen Compounds Using Quaternary Ammonium Salts as Starting Material". Journal of Chemistry 2017 (2017): 1–6. http://dx.doi.org/10.1155/2017/4586463.
Texto completoMasdeu, Carme, Maria Fuertes, Endika Martin-Encinas, Asier Selas, Gloria Rubiales, Francisco Palacios y Concepcion Alonso. "Fused 1,5-Naphthyridines: Synthetic Tools and Applications". Molecules 25, n.º 15 (31 de julio de 2020): 3508. http://dx.doi.org/10.3390/molecules25153508.
Texto completoLudwig, Miroslav, Iva Bednářová y Patrik Pařík. "Effect of Medium on Acid-Catalyzed Decomposition of N-(Phenylazo)-Substituted Nitrogen Heterocycles". Collection of Czechoslovak Chemical Communications 64, n.º 10 (1999): 1654–72. http://dx.doi.org/10.1135/cccc19991654.
Texto completoGeorghiou, Paris E. "Preface". Pure and Applied Chemistry 82, n.º 9 (1 de enero de 2010): iv. http://dx.doi.org/10.1351/pac20108209iv.
Texto completoWang, Min, Zi-Qiang Rong y Yu Zhao. "Stereoselective synthesis of ε-lactones or spiro-heterocycles through NHC-catalyzed annulation: divergent reactivity by catalyst control". Chem. Commun. 50, n.º 97 (2014): 15309–12. http://dx.doi.org/10.1039/c4cc07788a.
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