Статті в журналах з теми "Isoquinoline"
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Mandrekar, Ketan S., and 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, no. 28 (2022): 17701–5. http://dx.doi.org/10.1039/d2ra02534e.
Повний текст джерелаYang, Chunmei, Guoqing Zhang, Senling Tang, Yang Pan, Huawu Shao, and Wei Jiao. "Dess–Martin Periodinane-Mediated Oxidative Coupling Reaction of Isoquinoline with Benzyl Bromide." Molecules 28, no. 3 (January 17, 2023): 923. http://dx.doi.org/10.3390/molecules28030923.
Повний текст джерелаKoketsu, Mamoru, Amol Sonawane, Yunnus Shaikh, and Dinesh Garud. "Synthesis of Isoquinoline-Fused Quinazolinones through Ag(I)-Catalyzed Cascade Annulation of 2-Aminobenzamides and 2-Alkynylbenzaldehydes." Synthesis 51, no. 02 (September 21, 2018): 500–507. http://dx.doi.org/10.1055/s-0037-1610910.
Повний текст джерелаMurtagh, Kevin, Brian A. Sweetman, and Patrick J. Guiry. "New chiral tridentate ligands for asymmetric catalysis." Pure and Applied Chemistry 78, no. 2 (January 1, 2006): 311–20. http://dx.doi.org/10.1351/pac200678020311.
Повний текст джерелаZhang, 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, no. 47 (2022): 30248–52. http://dx.doi.org/10.1039/d2ra06097c.
Повний текст джерелаWu, Wei, Yan Wang, Jing Guo, Liu Cai, Yuan Chen, Yanmin Huang та Yungui Peng. "Asymmetric acyl-Mannich reaction of isoquinolines with α-(diazomethyl)phosphonate and diazoacetate catalyzed by chiral Brønsted acids". Chemical Communications 56, № 76 (2020): 11235–38. http://dx.doi.org/10.1039/d0cc03201h.
Повний текст джерелаSloop, 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.
Повний текст джерелаLi, Jiu-ling, Wei-ze Li, Ying-chun Wang, Qiu Ren, Heng-shan Wang, and 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, no. 65 (2016): 10028–31. http://dx.doi.org/10.1039/c6cc03530b.
Повний текст джерелаAn, Yuanyuan, Hongguang Xia, and Jie Wu. "Base-controlled [3+3] cycloaddition of isoquinoline N-oxides with azaoxyallyl cations." Chemical Communications 52, no. 68 (2016): 10415–18. http://dx.doi.org/10.1039/c6cc03650c.
Повний текст джерелаClark, Robin D., Jahangir, and James A. Langston. "Heteroatom-directed lateral lithiation: synthesis of isoquinoline derivatives from N-(tert-butoxycarbonyl)-2-methylbenzylamines." Canadian Journal of Chemistry 72, no. 1 (January 1, 1994): 23–30. http://dx.doi.org/10.1139/v94-005.
Повний текст джерелаSolongo, A., R. Istatkova, S. Philipov, S. Javzan, and D. Selenge. "Phytochemical study on Berberis sibirica Pall." Mongolian Journal of Chemistry 12 (September 24, 2014): 117–22. http://dx.doi.org/10.5564/mjc.v12i0.185.
Повний текст джерелаHussain, S. Fazal, M. Tariq Siddiqui, and Maurice Shamma. "Berbidine: A Simple Isoquinoline-Isoquinolone Dimer." Journal of Natural Products 52, no. 2 (March 1989): 317–19. http://dx.doi.org/10.1021/np50062a016.
Повний текст джерелаHošt'álková, Anna, Zdeněk Novák, Milan Pour, Anna Jirošová, Lubomír Opletal, Jiří Kuneš, and Lucie Cahlíková. "Berbanine: A New Isoquinoline-Isoquinolone Alkaloid from Berberis Vulgaris (Berberidaceae)." Natural Product Communications 8, no. 4 (April 2013): 1934578X1300800. http://dx.doi.org/10.1177/1934578x1300800407.
Повний текст джерелаLaha, Joydev K., Ummehani Tinwala, and Mandeep Kaur Hunjan. "Minisci aroylation of N-heterocycles using choline persulfate in water under mild conditions." New Journal of Chemistry 45, no. 48 (2021): 22853–59. http://dx.doi.org/10.1039/d1nj05068k.
Повний текст джерелаNanaji, Yerramsetti, Seema Kirar, Sandip V. Pawar, and Ashok Kumar Yadav. "A mild and metal-free synthesis of 2- and 1-alkyl/aryl/dialkyl-aminoquinolines and isoquinolines." RSC Advances 10, no. 13 (2020): 7628–34. http://dx.doi.org/10.1039/c9ra10397j.
Повний текст джерелаYang, Xiaobo, Jiyang Jie, Haoyi Li та Meihui Piao. "Ir(iii)-catalyzed synthesis of isoquinolines from benzimidates and α-diazocarbonyl compounds". RSC Advances 6, № 62 (2016): 57371–74. http://dx.doi.org/10.1039/c6ra10045g.
Повний текст джерелаPearson, Stuart, Shaun Fillery, Kristin Goldberg, Julie Demeritt, Jonathan Eden, Jonathan Finlayson, and Anil Patel. "Synthesis of Indole-Dihydroisoquinoline Sulfonyl Ureas via Three-Component Reactions." Synthesis 50, no. 24 (August 20, 2018): 4963–81. http://dx.doi.org/10.1055/s-0037-1610223.
Повний текст джерелаWang, Xiao-Ling. "Tetrahydroepiberberine." Acta Crystallographica Section E Structure Reports Online 62, no. 4 (March 8, 2006): o1271—o1272. http://dx.doi.org/10.1107/s1600536806007471.
Повний текст джерелаZhu, Di, Wen-Kun Luo, Luo Yang, and 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, no. 34 (2017): 7112–16. http://dx.doi.org/10.1039/c7ob01539a.
Повний текст джерелаBalewski, Łukasz, Franciszek Sączewski, Maria Gdaniec, Anita Kornicka, Karolina Cicha, and Aleksandra Jalińska. "Synthesis and Fluorescent Properties of Novel Isoquinoline Derivatives." Molecules 24, no. 22 (November 10, 2019): 4070. http://dx.doi.org/10.3390/molecules24224070.
Повний текст джерелаHassaneen, Hamdi M., Wagnat W. Wardkhan, and 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, no. 8 (August 1, 2013): 895–904. http://dx.doi.org/10.5560/znb.2013-3101.
Повний текст джерелаLiu, Cheng-Mei, Fei-Hua Yao, Xin-Hua Lu, Xue-Xia Zhang, Lian-Xiang Luo, Xiao Liang, and Shu-Hua Qi. "Isoquinoline Alkaloids as Protein Tyrosine Phosphatase Inhibitors from a Deep-Sea-Derived Fungus Aspergillus puniceus." Marine Drugs 20, no. 1 (January 17, 2022): 78. http://dx.doi.org/10.3390/md20010078.
Повний текст джерелаHua, Ruimao. "Isoquinolone Syntheses by Annulation Protocols." Catalysts 11, no. 5 (May 11, 2021): 620. http://dx.doi.org/10.3390/catal11050620.
Повний текст джерелаAzad, Leila, Maryam Ghazvini, Haleh Sanaeishoar, and 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, no. 11-12 (August 30, 2019): 457–60. http://dx.doi.org/10.1177/1747519819871028.
Повний текст джерелаVorobyeva, Daria V., Dmitry A. Petropavlovskikh, Ivan A. Godovikov, Fedor M. Dolgushin та 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, № 23 (2 грудня 2022): 8488. http://dx.doi.org/10.3390/molecules27238488.
Повний текст джерелаKmieciak, Anna, Marta Ćwiklińska, Karolina Jeżak, Afef Shili, and Marek P. Krzemiński. "Searching for New Biologically Active Compounds Derived from Isoquinoline Alkaloids." Chemistry Proceedings 3, no. 1 (November 14, 2020): 97. http://dx.doi.org/10.3390/ecsoc-24-08417.
Повний текст джерелаHensen, K., R. Mayr-Stein, and M. Bolte. "Isoquinoline." Acta Crystallographica Section C Crystal Structure Communications 55, no. 9 (September 15, 1999): 1565–67. http://dx.doi.org/10.1107/s0108270199006320.
Повний текст джерелаShih, Tzenge-Lien, Min-Chen Tsai, Pei Huang, and Liang Syu. "Synthesis of Novel Isoquinolino[5,4-ab]phenanthridine Derivatives via Pictet–Spengler Reaction." Synthesis 51, no. 06 (November 21, 2018): 1377–82. http://dx.doi.org/10.1055/s-0037-1610670.
Повний текст джерелаObydennik, Arina Y., Alexander A. Titov, Anna V. Listratova, Tatiana N. Borisova, Victor B. Rybakov, Leonid G. Voskressensky, and Alexey V. Varlamov. "Concise and Free-Metal Access to Lactone-Annelated Pyrrolo[2,1-a]isoquinoline Derivatives via a 1,2-Rearrangement Step." International Journal of Molecular Sciences 25, no. 2 (January 16, 2024): 1085. http://dx.doi.org/10.3390/ijms25021085.
Повний текст джерелаKratzer, Philipp, Susanne Steinhauser, and Gerhard Maas. "Propyne Iminium Salts and Isoquinoline – 1 : 1 and 2 : 1 Adducts." Zeitschrift für Naturforschung B 69, no. 5 (May 1, 2014): 567–79. http://dx.doi.org/10.5560/znb.2014-4032.
Повний текст джерелаHajinasiri, Rahimeh, and 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, no. 7 (July 1, 2013): 818–22. http://dx.doi.org/10.5560/znb.2013-3095.
Повний текст джерелаPotikha, Lyudmyla, Volodymyr Brovarets, and Victor Zhirnov. "Biological Evaluation of 3-Aminoisoquinolin-1(2H)-one Derivatives as Potential Anticancer Agents Authors Lyudmyla Potikha." French-Ukrainian Journal of Chemistry 9, no. 2 (2021): 52–63. http://dx.doi.org/10.17721/fujcv9i2p52-63.
Повний текст джерелаLantos, Ivan, and Haralambos E. Katerinopoulos. "Synthetic transformations of cyclopropyl annulated dihydroisoquinolines." Canadian Journal of Chemistry 69, no. 6 (June 1, 1991): 1033–37. http://dx.doi.org/10.1139/v91-152.
Повний текст джерелаAltshuler, Heinrich N., Galina Yu Shkurenko, and Sergey Yu Lyrschikov. "Encapsulation of isoquinoline in a polymer nanocontainer based on the CU-2-4 sulfocationite." Butlerov Communications 61, no. 2 (February 29, 2020): 97–102. http://dx.doi.org/10.37952/roi-jbc-01/20-61-2-97.
Повний текст джерелаDefois, Mathilde, Chloé Rémondin, Béatrice Josselin, Lionel Nauton, Vincent Théry, Fabrice Anizon, Sandrine Ruchaud, Francis Giraud, and Pascale Moreau. "Synthesis and Kinase Inhibitory Potencies of Pyrazolo[3,4-g]isoquinolines." Molecules 27, no. 17 (August 30, 2022): 5578. http://dx.doi.org/10.3390/molecules27175578.
Повний текст джерелаLiu, Yi Bin, Yu Zhen Li, and Xue Ding. "Adsorption Simulation of Basic Nitrogen Compounds in ZSM-5 and USY Zeolites by Grand Canonical Monte Carlo Method." Advanced Materials Research 1096 (April 2015): 189–93. http://dx.doi.org/10.4028/www.scientific.net/amr.1096.189.
Повний текст джерелаZhang, Yangyang, Yun Kang, Hui Xie, Yaqin Wang, Yaoting Li, and Jianming Huang. "Comparative Transcriptome Analysis Reveals Candidate Genes Involved in Isoquinoline Alkaloid Biosynthesis in Stephania tetrandra." Planta Medica 86, no. 17 (August 5, 2020): 1258–68. http://dx.doi.org/10.1055/a-1209-3407.
Повний текст джерелаE, Yong Sheng. "Extraction and Purification of Isoquinoline from Wash Oil." Advanced Materials Research 791-793 (September 2013): 93–96. http://dx.doi.org/10.4028/www.scientific.net/amr.791-793.93.
Повний текст джерелаZhao, Yun-Hui, Zhihua Zhou, Yong-Cheng Ma, Yueyang Luo, Yingli Zhu, Hang Wang, Hangbin Zhou, Hailong Tan, Wenlin Xie, and 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, no. 06 (January 2, 2018): 773–78. http://dx.doi.org/10.1055/s-0036-1591743.
Повний текст джерелаAislabie, J., N. K. Richards, and T. C. Lyttle. "Description of bacteria able to degrade isoquinoline in pure culture." Canadian Journal of Microbiology 40, no. 7 (July 1, 1994): 555–60. http://dx.doi.org/10.1139/m94-089.
Повний текст джерелаMin, Xinyi, Ting Zhu, Xinyi Hu, Cong Hou, Jianing He, and Xia Liu. "Transcriptome and Metabolome Analysis of Isoquinoline Alkaloid Biosynthesis of Coptis chinensis in Different Years." Genes 14, no. 12 (December 18, 2023): 2232. http://dx.doi.org/10.3390/genes14122232.
Повний текст джерелаPossner, Sven T., Frank C. Schroeder, Hans Tore Rapp, Volker Sinnwell, Stefan Franke, and Wittko Francke. "3,7-Isoquinoline quinones from the ascidian tunicate Ascidia virginea." Zeitschrift für Naturforschung C 72, no. 7-8 (July 14, 2017): 259–64. http://dx.doi.org/10.1515/znc-2017-0012.
Повний текст джерелаNiopas, Ioannis, and Gordon A. Smail. "N-substituted tricyclic isoquinoline hydantoins." Collection of Czechoslovak Chemical Communications 55, no. 2 (1990): 540–45. http://dx.doi.org/10.1135/cccc19900540.
Повний текст джерелаKostova, Nadezhda, and Tsvetelina Doncheva. "Hypecoum spp.—Chemistry and Biological Activity of Alkaloids." Diversity 15, no. 9 (September 19, 2023): 1023. http://dx.doi.org/10.3390/d15091023.
Повний текст джерелаDonati, C., TV Hung, and RH Prager. "The Chemistry of Phthalide-3-carboxylic Acid. VII. Reaction With Isoquinoline Derivatives." Australian Journal of Chemistry 43, no. 2 (1990): 375. http://dx.doi.org/10.1071/ch9900375.
Повний текст джерелаRichards, N. K., H. K. Mahanty, and J. Aislabie. "Construction of a DNA probe to detect isoquinoline-degrading bacteria." Canadian Journal of Microbiology 40, no. 7 (July 1, 1994): 561–66. http://dx.doi.org/10.1139/m94-090.
Повний текст джерелаJankowski, Christopher K., Gaëtan LeClair, Jacqueline MR Bélanger, Jocelyn RJ Paré, and Marie-Rose VanCalsteren. "Microwave-assisted Diels-Alder synthesis." Canadian Journal of Chemistry 79, no. 12 (December 1, 2001): 1906–9. http://dx.doi.org/10.1139/v01-183.
Повний текст джерелаTantawy, Mohamed A., Farid M. Sroor, Magda F. Mohamed, Mostafa E. El-Naggar, Fatma M. Saleh, Hamdi M. Hassaneen, and 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, no. 1 (April 10, 2020): 70–83. http://dx.doi.org/10.2174/1871520619666191024121116.
Повний текст джерелаYoung, Steven D., J. Mark Wiggins, and Joel R. Huff. "3,4-Dihydrobenz[f]isoquinoline and 3,4-dihydrobenz[g]isoquinoline." Journal of Organic Chemistry 53, no. 5 (March 1988): 1114–16. http://dx.doi.org/10.1021/jo00240a042.
Повний текст джерелаYao, Bo, Chen-Liang Deng, Yan Liu, Ri-Yuan Tang, Xing-Guo Zhang, and Jin-Heng Li. "Palladium-catalyzed oxidative carbamoylation of isoquinoline N-oxides with formylamides by means of dual C–H oxidative coupling." Chemical Communications 51, no. 19 (2015): 4097–100. http://dx.doi.org/10.1039/c4cc10140e.
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