Artículos de revistas sobre el tema "Isoquinoline"
Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros
Consulte los 50 mejores artículos de revistas para su investigación sobre el tema "Isoquinoline".
Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.
También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.
Explore artículos de revistas sobre una amplia variedad de disciplinas y organice su bibliografía correctamente.
Mandrekar, Ketan S. y Santosh G. Tilve. "P4O10/TfOH mediated domino condensation–cyclization of amines with diacids: a route to indolizidine alkaloids under catalyst- and solvent-free conditions". RSC Advances 12, n.º 28 (2022): 17701–5. http://dx.doi.org/10.1039/d2ra02534e.
Texto completoYang, Chunmei, Guoqing Zhang, Senling Tang, Yang Pan, Huawu Shao y Wei Jiao. "Dess–Martin Periodinane-Mediated Oxidative Coupling Reaction of Isoquinoline with Benzyl Bromide". Molecules 28, n.º 3 (17 de enero de 2023): 923. http://dx.doi.org/10.3390/molecules28030923.
Texto completoKoketsu, Mamoru, Amol Sonawane, Yunnus Shaikh y Dinesh Garud. "Synthesis of Isoquinoline-Fused Quinazolinones through Ag(I)-Catalyzed Cascade Annulation of 2-Aminobenzamides and 2-Alkynylbenzaldehydes". Synthesis 51, n.º 02 (21 de septiembre de 2018): 500–507. http://dx.doi.org/10.1055/s-0037-1610910.
Texto completoZhang, Lujun, Wenfang Xiong, Biao Yao, Haitao Liu, Meng Li, Yu Qin, Yujian Yu et al. "Facile synthesis of isoquinolines and isoquinoline N-oxides via a copper-catalyzed intramolecular cyclization in water". RSC Advances 12, n.º 47 (2022): 30248–52. http://dx.doi.org/10.1039/d2ra06097c.
Texto completoMurtagh, Kevin, Brian A. Sweetman y Patrick J. Guiry. "New chiral tridentate ligands for asymmetric catalysis". Pure and Applied Chemistry 78, n.º 2 (1 de enero de 2006): 311–20. http://dx.doi.org/10.1351/pac200678020311.
Texto completoWu, Wei, Yan Wang, Jing Guo, Liu Cai, Yuan Chen, Yanmin Huang y Yungui Peng. "Asymmetric acyl-Mannich reaction of isoquinolines with α-(diazomethyl)phosphonate and diazoacetate catalyzed by chiral Brønsted acids". Chemical Communications 56, n.º 76 (2020): 11235–38. http://dx.doi.org/10.1039/d0cc03201h.
Texto completoSloop, Joseph C. "Advances in the Preparation of Fluorinated Isoquinolines: A Decade of Progress". Journal of Chemistry 2017 (2017): 1–15. http://dx.doi.org/10.1155/2017/2860123.
Texto completoLi, Jiu-ling, Wei-ze Li, Ying-chun Wang, Qiu Ren, Heng-shan Wang y Ying-ming Pan. "Palladium(ii)-catalyzed C–C and C–O bond formation for the synthesis of C1-benzoyl isoquinolines from isoquinoline N-oxides and nitroalkenes". Chemical Communications 52, n.º 65 (2016): 10028–31. http://dx.doi.org/10.1039/c6cc03530b.
Texto completoAn, Yuanyuan, Hongguang Xia y Jie Wu. "Base-controlled [3+3] cycloaddition of isoquinoline N-oxides with azaoxyallyl cations". Chemical Communications 52, n.º 68 (2016): 10415–18. http://dx.doi.org/10.1039/c6cc03650c.
Texto completoHussain, S. Fazal, M. Tariq Siddiqui y Maurice Shamma. "Berbidine: A Simple Isoquinoline-Isoquinolone Dimer". Journal of Natural Products 52, n.º 2 (marzo de 1989): 317–19. http://dx.doi.org/10.1021/np50062a016.
Texto completoClark, Robin D., Jahangir y James A. Langston. "Heteroatom-directed lateral lithiation: synthesis of isoquinoline derivatives from N-(tert-butoxycarbonyl)-2-methylbenzylamines". Canadian Journal of Chemistry 72, n.º 1 (1 de enero de 1994): 23–30. http://dx.doi.org/10.1139/v94-005.
Texto completoSolongo, A., R. Istatkova, S. Philipov, S. Javzan y D. Selenge. "Phytochemical study on Berberis sibirica Pall." Mongolian Journal of Chemistry 12 (24 de septiembre de 2014): 117–22. http://dx.doi.org/10.5564/mjc.v12i0.185.
Texto completoHošt'álková, Anna, Zdeněk Novák, Milan Pour, Anna Jirošová, Lubomír Opletal, Jiří Kuneš y Lucie Cahlíková. "Berbanine: A New Isoquinoline-Isoquinolone Alkaloid from Berberis Vulgaris (Berberidaceae)". Natural Product Communications 8, n.º 4 (abril de 2013): 1934578X1300800. http://dx.doi.org/10.1177/1934578x1300800407.
Texto completoLaha, Joydev K., Ummehani Tinwala y Mandeep Kaur Hunjan. "Minisci aroylation of N-heterocycles using choline persulfate in water under mild conditions". New Journal of Chemistry 45, n.º 48 (2021): 22853–59. http://dx.doi.org/10.1039/d1nj05068k.
Texto completoNanaji, Yerramsetti, Seema Kirar, Sandip V. Pawar y Ashok Kumar Yadav. "A mild and metal-free synthesis of 2- and 1-alkyl/aryl/dialkyl-aminoquinolines and isoquinolines". RSC Advances 10, n.º 13 (2020): 7628–34. http://dx.doi.org/10.1039/c9ra10397j.
Texto completoYang, Xiaobo, Jiyang Jie, Haoyi Li y Meihui Piao. "Ir(iii)-catalyzed synthesis of isoquinolines from benzimidates and α-diazocarbonyl compounds". RSC Advances 6, n.º 62 (2016): 57371–74. http://dx.doi.org/10.1039/c6ra10045g.
Texto completoPearson, Stuart, Shaun Fillery, Kristin Goldberg, Julie Demeritt, Jonathan Eden, Jonathan Finlayson y Anil Patel. "Synthesis of Indole-Dihydroisoquinoline Sulfonyl Ureas via Three-Component Reactions". Synthesis 50, n.º 24 (20 de agosto de 2018): 4963–81. http://dx.doi.org/10.1055/s-0037-1610223.
Texto completoWang, Xiao-Ling. "Tetrahydroepiberberine". Acta Crystallographica Section E Structure Reports Online 62, n.º 4 (8 de marzo de 2006): o1271—o1272. http://dx.doi.org/10.1107/s1600536806007471.
Texto completoZhu, Di, Wen-Kun Luo, Luo Yang y Da-You Ma. "Iodine-catalyzed oxidative multiple C–H bond functionalization of isoquinolines with methylarenes: an efficient synthesis of isoquinoline-1,3,4(2H)-triones". Organic & Biomolecular Chemistry 15, n.º 34 (2017): 7112–16. http://dx.doi.org/10.1039/c7ob01539a.
Texto completoBalewski, Łukasz, Franciszek Sączewski, Maria Gdaniec, Anita Kornicka, Karolina Cicha y Aleksandra Jalińska. "Synthesis and Fluorescent Properties of Novel Isoquinoline Derivatives". Molecules 24, n.º 22 (10 de noviembre de 2019): 4070. http://dx.doi.org/10.3390/molecules24224070.
Texto completoHassaneen, Hamdi M., Wagnat W. Wardkhan y Yasmin Sh Mohammed. "A Novel Route to Isoquinoline[2,1-g][1,6]naphthyridine, Pyrazolo[5,1-a] isoquinoline and Pyridazino[4´,5´:3,4]pyrazolo[5,1-a]isoquinoline Derivatives With Evaluation of Antitumor Activities". Zeitschrift für Naturforschung B 68, n.º 8 (1 de agosto de 2013): 895–904. http://dx.doi.org/10.5560/znb.2013-3101.
Texto completoHua, Ruimao. "Isoquinolone Syntheses by Annulation Protocols". Catalysts 11, n.º 5 (11 de mayo de 2021): 620. http://dx.doi.org/10.3390/catal11050620.
Texto completoLiu, Cheng-Mei, Fei-Hua Yao, Xin-Hua Lu, Xue-Xia Zhang, Lian-Xiang Luo, Xiao Liang y Shu-Hua Qi. "Isoquinoline Alkaloids as Protein Tyrosine Phosphatase Inhibitors from a Deep-Sea-Derived Fungus Aspergillus puniceus". Marine Drugs 20, n.º 1 (17 de enero de 2022): 78. http://dx.doi.org/10.3390/md20010078.
Texto completoAzad, Leila, Maryam Ghazvini, Haleh Sanaeishoar y Issa Yavari. "Synthesis of functionalized 1,2-dihydroisoquinolines via one-pot reactions of isoquinoline, alkyl propiolate, and thiazolidin-2,4-dione". Journal of Chemical Research 43, n.º 11-12 (30 de agosto de 2019): 457–60. http://dx.doi.org/10.1177/1747519819871028.
Texto completoVorobyeva, Daria V., Dmitry A. Petropavlovskikh, Ivan A. Godovikov, Fedor M. Dolgushin y Sergey N. Osipov. "Synthesis of Functionalized Isoquinolone Derivatives via Rh(III)-Catalyzed [4+2]-Annulation of Benzamides with Internal Acetylene-Containing α-CF3-α-Amino Carboxylates". Molecules 27, n.º 23 (2 de diciembre de 2022): 8488. http://dx.doi.org/10.3390/molecules27238488.
Texto completoKmieciak, Anna, Marta Ćwiklińska, Karolina Jeżak, Afef Shili y Marek P. Krzemiński. "Searching for New Biologically Active Compounds Derived from Isoquinoline Alkaloids". Chemistry Proceedings 3, n.º 1 (14 de noviembre de 2020): 97. http://dx.doi.org/10.3390/ecsoc-24-08417.
Texto completoHensen, K., R. Mayr-Stein y M. Bolte. "Isoquinoline". Acta Crystallographica Section C Crystal Structure Communications 55, n.º 9 (15 de septiembre de 1999): 1565–67. http://dx.doi.org/10.1107/s0108270199006320.
Texto completoShih, Tzenge-Lien, Min-Chen Tsai, Pei Huang y Liang Syu. "Synthesis of Novel Isoquinolino[5,4-ab]phenanthridine Derivatives via Pictet–Spengler Reaction". Synthesis 51, n.º 06 (21 de noviembre de 2018): 1377–82. http://dx.doi.org/10.1055/s-0037-1610670.
Texto completoHajinasiri, Rahimeh y Sobhan Rezayati. "Solvent-free Synthesis of 1,2-Disubstituted Derivatives of 1,2- Dihydroisoquinoline, 1,2-Dihydroquinoline and 1,2-Dihydropyridine". Zeitschrift für Naturforschung B 68, n.º 7 (1 de julio de 2013): 818–22. http://dx.doi.org/10.5560/znb.2013-3095.
Texto completoKratzer, Philipp, Susanne Steinhauser y Gerhard Maas. "Propyne Iminium Salts and Isoquinoline – 1 : 1 and 2 : 1 Adducts". Zeitschrift für Naturforschung B 69, n.º 5 (1 de mayo de 2014): 567–79. http://dx.doi.org/10.5560/znb.2014-4032.
Texto completoPotikha, Lyudmyla, Volodymyr Brovarets y Victor Zhirnov. "Biological Evaluation of 3-Aminoisoquinolin-1(2H)-one Derivatives as Potential Anticancer Agents Authors Lyudmyla Potikha". French-Ukrainian Journal of Chemistry 9, n.º 2 (2021): 52–63. http://dx.doi.org/10.17721/fujcv9i2p52-63.
Texto completoLantos, Ivan y Haralambos E. Katerinopoulos. "Synthetic transformations of cyclopropyl annulated dihydroisoquinolines". Canadian Journal of Chemistry 69, n.º 6 (1 de junio de 1991): 1033–37. http://dx.doi.org/10.1139/v91-152.
Texto completoAltshuler, Heinrich N., Galina Yu Shkurenko y Sergey Yu Lyrschikov. "Encapsulation of isoquinoline in a polymer nanocontainer based on the CU-2-4 sulfocationite". Butlerov Communications 61, n.º 2 (29 de febrero de 2020): 97–102. http://dx.doi.org/10.37952/roi-jbc-01/20-61-2-97.
Texto completoDefois, Mathilde, Chloé Rémondin, Béatrice Josselin, Lionel Nauton, Vincent Théry, Fabrice Anizon, Sandrine Ruchaud, Francis Giraud y Pascale Moreau. "Synthesis and Kinase Inhibitory Potencies of Pyrazolo[3,4-g]isoquinolines". Molecules 27, n.º 17 (30 de agosto de 2022): 5578. http://dx.doi.org/10.3390/molecules27175578.
Texto completoLiu, Yi Bin, Yu Zhen Li y Xue Ding. "Adsorption Simulation of Basic Nitrogen Compounds in ZSM-5 and USY Zeolites by Grand Canonical Monte Carlo Method". Advanced Materials Research 1096 (abril de 2015): 189–93. http://dx.doi.org/10.4028/www.scientific.net/amr.1096.189.
Texto completoZhang, Yangyang, Yun Kang, Hui Xie, Yaqin Wang, Yaoting Li y Jianming Huang. "Comparative Transcriptome Analysis Reveals Candidate Genes Involved in Isoquinoline Alkaloid Biosynthesis in Stephania tetrandra". Planta Medica 86, n.º 17 (5 de agosto de 2020): 1258–68. http://dx.doi.org/10.1055/a-1209-3407.
Texto completoE, Yong Sheng. "Extraction and Purification of Isoquinoline from Wash Oil". Advanced Materials Research 791-793 (septiembre de 2013): 93–96. http://dx.doi.org/10.4028/www.scientific.net/amr.791-793.93.
Texto completoZhao, Yun-Hui, Zhihua Zhou, Yong-Cheng Ma, Yueyang Luo, Yingli Zhu, Hang Wang, Hangbin Zhou, Hailong Tan, Wenlin Xie y Zilong Tang. "Synthesis of Potential Anticancer 1-(1H-Indol-3-yl)isoquinolines by Silver Nitrate Mediated Tandem Reactions of 2-Alkynylbenzaldehyde Azines and Indoles". Synlett 29, n.º 06 (2 de enero de 2018): 773–78. http://dx.doi.org/10.1055/s-0036-1591743.
Texto completoAislabie, J., N. K. Richards y T. C. Lyttle. "Description of bacteria able to degrade isoquinoline in pure culture". Canadian Journal of Microbiology 40, n.º 7 (1 de julio de 1994): 555–60. http://dx.doi.org/10.1139/m94-089.
Texto completoPossner, Sven T., Frank C. Schroeder, Hans Tore Rapp, Volker Sinnwell, Stefan Franke y Wittko Francke. "3,7-Isoquinoline quinones from the ascidian tunicate Ascidia virginea". Zeitschrift für Naturforschung C 72, n.º 7-8 (14 de julio de 2017): 259–64. http://dx.doi.org/10.1515/znc-2017-0012.
Texto completoNiopas, Ioannis y Gordon A. Smail. "N-substituted tricyclic isoquinoline hydantoins". Collection of Czechoslovak Chemical Communications 55, n.º 2 (1990): 540–45. http://dx.doi.org/10.1135/cccc19900540.
Texto completoDonati, C., TV Hung y RH Prager. "The Chemistry of Phthalide-3-carboxylic Acid. VII. Reaction With Isoquinoline Derivatives". Australian Journal of Chemistry 43, n.º 2 (1990): 375. http://dx.doi.org/10.1071/ch9900375.
Texto completoRichards, N. K., H. K. Mahanty y J. Aislabie. "Construction of a DNA probe to detect isoquinoline-degrading bacteria". Canadian Journal of Microbiology 40, n.º 7 (1 de julio de 1994): 561–66. http://dx.doi.org/10.1139/m94-090.
Texto completoJankowski, Christopher K., Gaëtan LeClair, Jacqueline MR Bélanger, Jocelyn RJ Paré y Marie-Rose VanCalsteren. "Microwave-assisted Diels-Alder synthesis". Canadian Journal of Chemistry 79, n.º 12 (1 de diciembre de 2001): 1906–9. http://dx.doi.org/10.1139/v01-183.
Texto completoYoung, Steven D., J. Mark Wiggins y Joel R. Huff. "3,4-Dihydrobenz[f]isoquinoline and 3,4-dihydrobenz[g]isoquinoline". Journal of Organic Chemistry 53, n.º 5 (marzo de 1988): 1114–16. http://dx.doi.org/10.1021/jo00240a042.
Texto completoTantawy, Mohamed A., Farid M. Sroor, Magda F. Mohamed, Mostafa E. El-Naggar, Fatma M. Saleh, Hamdi M. Hassaneen y Ismail A. Abdelhamid. "Molecular Docking Study, Cytotoxicity, Cell Cycle Arrest and Apoptotic Induction of Novel Chalcones Incorporating Thiadiazolyl Isoquinoline in Cervical Cancer". Anti-Cancer Agents in Medicinal Chemistry 20, n.º 1 (10 de abril de 2020): 70–83. http://dx.doi.org/10.2174/1871520619666191024121116.
Texto completoYao, Bo, Chen-Liang Deng, Yan Liu, Ri-Yuan Tang, Xing-Guo Zhang y Jin-Heng Li. "Palladium-catalyzed oxidative carbamoylation of isoquinoline N-oxides with formylamides by means of dual C–H oxidative coupling". Chemical Communications 51, n.º 19 (2015): 4097–100. http://dx.doi.org/10.1039/c4cc10140e.
Texto completoNi, Hengjia, Yordan Martínez, Guiping Guan, Román Rodríguez, Dairon Más, Hanhui Peng, Manuel Valdivié Navarro y Gang Liu. "Analysis of the Impact of Isoquinoline Alkaloids, Derived fromMacleaya cordataExtract, on the Development and Innate Immune Response in Swine and Poultry". BioMed Research International 2016 (2016): 1–7. http://dx.doi.org/10.1155/2016/1352146.
Texto completoYavari, Issa, Mohammad Piltan y Loghman Moradi. "Synthesis of pyrrolo[2,1-a]isoquinolines from activated acetylenes, benzoylnitromethanes, and isoquinoline". Tetrahedron 65, n.º 10 (marzo de 2009): 2067–71. http://dx.doi.org/10.1016/j.tet.2009.01.001.
Texto completoBremner, JB, CL Raston, GL Rowbottom, AH White y KN Winzenberg. "A Ring Destruction Approach to Some Benzo-Fused Medium-Sized Heterocycles by Means of Cyanogen-Bromide Under Solvolytic Conditions - X-Ray Structure of a '1h-2,6-Benzoxazecine-6-Carbonitrile and a '2h-3,6-Benzoxazecine-6-Carbonitrile Derivative". Australian Journal of Chemistry 39, n.º 6 (1986): 893. http://dx.doi.org/10.1071/ch9860893.
Texto completo