Artículos de revistas sobre el tema "Isocryptolepine"
Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros
Consulte los 49 mejores artículos de revistas para su investigación sobre el tema "Isocryptolepine".
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.
Wang, Ning, Marta Świtalska, Li Wang, Elkhabiry Shaban, Md Imran Hossain, Ibrahim El Tantawy El Sayed, Joanna Wietrzyk y Tsutomu Inokuchi. "Structural Modifications of Nature-Inspired Indoloquinolines: A Mini Review of Their Potential Antiproliferative Activity". Molecules 24, n.º 11 (5 de junio de 2019): 2121. http://dx.doi.org/10.3390/molecules24112121.
Texto completoMurray, Paul E., Keith Mills y John A. Joule. "A Synthesis of Isocryptolepine". Journal of Chemical Research, n.º 7 (1998): 377. http://dx.doi.org/10.1039/a801313f.
Texto completoPousset, Jean-Louis, Marie-Therese Martin, Akino Jossang y Bernard Bodo. "Isocryptolepine from Cryptolepis sanguinolenta". Phytochemistry 39, n.º 3 (junio de 1995): 735–36. http://dx.doi.org/10.1016/0031-9422(94)00925-j.
Texto completoAksenov, Alexander V., Dmitrii A. Aksenov, Georgii D. Griaznov, Nicolai A. Aksenov, Leonid G. Voskressensky y Michael Rubin. "Unexpected cyclization of 2-(2-aminophenyl)indoles with nitroalkenes to furnish indolo[3,2-c]quinolines". Organic & Biomolecular Chemistry 16, n.º 23 (2018): 4325–32. http://dx.doi.org/10.1039/c8ob00588e.
Texto completoMurray, Paul E., Keith Mills y John A. Joule. "ChemInform Abstract: A Synthesis of Isocryptolepine." ChemInform 30, n.º 15 (16 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199915254.
Texto completoAkitake, Masahiro, Shizuki Noda, Kohei Miyoshi, Motohiro Sonoda y Shinji Tanimori. "Access to γ-Carbolines: Synthesis of Isocryptolepine". Journal of Organic Chemistry 86, n.º 24 (6 de diciembre de 2021): 17727–37. http://dx.doi.org/10.1021/acs.joc.1c02026.
Texto completoKraus, George A. y Haitao Guo. "A direct synthesis of neocryptolepine and isocryptolepine". Tetrahedron Letters 51, n.º 31 (agosto de 2010): 4137–39. http://dx.doi.org/10.1016/j.tetlet.2010.05.141.
Texto completoDubovitskii, S. V., O. S. Radchenko y V. L. Norikov. "Synthesis of isocryptolepine, an alkaloid fromCryptolepis sanguinolenta". Russian Chemical Bulletin 45, n.º 11 (noviembre de 1996): 2656–57. http://dx.doi.org/10.1007/bf01431136.
Texto completoHelgeland, Ida y Magne Sydnes. "A Concise Synthesis of Isocryptolepine by C–C Cross-Coupling Followed by a Tandem C–H Activation and C–N Bond Formation". SynOpen 01, n.º 01 (marzo de 2017): 0041–44. http://dx.doi.org/10.1055/s-0036-1590807.
Texto completoWhittell, Louise R., Kevin T. Batty, Rina P. M. Wong, Erin M. Bolitho, Simon A. Fox, Timothy M. E. Davis y Paul E. Murray. "Synthesis and antimalarial evaluation of novel isocryptolepine derivatives". Bioorganic & Medicinal Chemistry 19, n.º 24 (diciembre de 2011): 7519–25. http://dx.doi.org/10.1016/j.bmc.2011.10.037.
Texto completoLi, Jun-cai, Ren-xuan Wang, Yu Sun, Jia-kai Zhu, Guan-fang Hu, Yu-ling Wang, Rui Zhou et al. "Design, synthesis and antifungal activity evaluation of isocryptolepine derivatives". Bioorganic Chemistry 92 (noviembre de 2019): 103266. http://dx.doi.org/10.1016/j.bioorg.2019.103266.
Texto completoRujimongkon, Kitiya, Mathirut Mungthin, Jumreang Tummatorn, Sumate Ampawong, Poom Adisakwattana, Usa Boonyuen y Onrapak Reamtong. "Proteomic analysis of Plasmodium falciparum response to isocryptolepine derivative". PLOS ONE 14, n.º 8 (8 de agosto de 2019): e0220871. http://dx.doi.org/10.1371/journal.pone.0220871.
Texto completoGrellier, Phillippe, Lobo Ramiaramanana, Valérie Millerioux, Eric Deharo, Joseph Schrével, François Frappier, François Trigalo, Bernard Bodo y Jean-Louis Pousset. "Antimalarial Activity of Cryptolepine and Isocryptolepine, Alkaloids Isolated fromCryptolepis sanguinolenta". Phytotherapy Research 10, n.º 4 (junio de 1996): 317–21. http://dx.doi.org/10.1002/(sici)1099-1573(199606)10:4<317::aid-ptr858>3.0.co;2-0.
Texto completoDUBOVITSKII, S. V., O. S. RADCHENKO y V. L. NOVIKOV. "ChemInform Abstract: Synthesis of Isocryptolepine, an Alkaloid from Cryptolepis sanguinolenta." ChemInform 28, n.º 17 (4 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199717217.
Texto completoRodphon, Warabhorn, Pavitra Laohapaisan, Nantamon Supantanapong, Onrapak Reamtong, Lukana Ngiwsara, Kriengsak Lirdprapamongkol, Charnsak Thongsornkleeb et al. "Synthesis of Isocryptolepine‐Triazole Adducts and Evaluation of Their Cytotoxic Activity". ChemMedChem 16, n.º 24 (14 de octubre de 2021): 3750–62. http://dx.doi.org/10.1002/cmdc.202100554.
Texto completoAksenov, Alexander V., Dmitrii A. Aksenov, Naila A. Orazova, Nicolai A. Aksenov, Georgii D. Griaznov, Annelise De Carvalho, Robert Kiss, Véronique Mathieu, Alexander Kornienko y Michael Rubin. "One-Pot, Three-Component Assembly of Indoloquinolines: Total Synthesis of Isocryptolepine". Journal of Organic Chemistry 82, n.º 6 (8 de marzo de 2017): 3011–18. http://dx.doi.org/10.1021/acs.joc.6b03084.
Texto completoT. Parvatkar, Prakash, Perunninakulath S. Parameswaran y Santosh G. Tilve. "Isolation, Biological Activities and Synthesis of Indoloquinoline Alkaloids: Cryptolepine, Isocryptolepine and Neocryptolepine". Current Organic Chemistry 15, n.º 7 (1 de abril de 2011): 1036–57. http://dx.doi.org/10.2174/138527211794785118.
Texto completoThobokholt, Elida N., Enrique L. Larghi, Andrea B. J. Bracca y Teodoro S. Kaufman. "Isolation and synthesis of cryptosanguinolentine (isocryptolepine), a naturally-occurring bioactive indoloquinoline alkaloid". RSC Advances 10, n.º 32 (2020): 18978–9002. http://dx.doi.org/10.1039/d0ra03096a.
Texto completoAggrey, Mike Okweesi, Hui-Hui Li, Wen-Qiong Wang, Weibin Song, Yiping Wang y Li-Jiang Xuan. "Isocryptolepine, an indoloquinoline alkaloid from Cryptolepis sanguinolenta promotes LDL uptake in HepG2 cells". Revista Brasileira de Farmacognosia 28, n.º 6 (noviembre de 2018): 654–57. http://dx.doi.org/10.1016/j.bjp.2018.08.008.
Texto completoKraus, George, Haitao Guo, Ganesh Kumar, Gerald Pollock III, Heather Carruthers, Divya Chaudhary y Jonathan Beasley. "A Flexible Synthesis of Indoles from ortho-Substituted Anilines: A Direct Synthesis of Isocryptolepine". Synthesis 2010, n.º 08 (24 de marzo de 2010): 1386–93. http://dx.doi.org/10.1055/s-0029-1218706.
Texto completoKraus, George, Haitao Guo, Ganesh Kumar, Heather Carruthers, Divya Chaudhary y Jonathan Beasley. "A Flexible Synthesis of Indoles from ortho-Substituted Anilines: A Direct Synthesis of Isocryptolepine". Synthesis 2010, n.º 14 (julio de 2010): 2496. http://dx.doi.org/10.1055/s-0029-1218853.
Texto completoParvatkar, Prakash T., Perunninakulath S. Parameswaran y Santosh G. Tilve. "ChemInform Abstract: Isolation, Biological Activities, and Synthesis of Indoloquinoline Alkaloids: Cryptolepine, Isocryptolepine, and Neocryptolepine". ChemInform 42, n.º 38 (25 de agosto de 2011): no. http://dx.doi.org/10.1002/chin.201138237.
Texto completoAroonkit, Pasuk, Charnsak Thongsornkleeb, Jumreang Tummatorn, Suppachai Krajangsri, Mathirut Mungthin y Somsak Ruchirawat. "Synthesis of isocryptolepine analogues and their structure–activity relationship studies as antiplasmodial and antiproliferative agents". European Journal of Medicinal Chemistry 94 (abril de 2015): 56–62. http://dx.doi.org/10.1016/j.ejmech.2015.02.047.
Texto completoKraus, George A., Haitao Guo, Ganesh Kumar, Gerald III Pollock, Heather Carruthers, Divya Chaudhary y Jonathan Beasley. "ChemInform Abstract: A Flexible Synthesis of Indoles from ortho-Substituted Anilines: A Direct Synthesis of Isocryptolepine." ChemInform 41, n.º 35 (5 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.201035120.
Texto completoMurugan, Arumugavel, Shinde Vidyacharan, Ruma Ghosh y Duddu S. Sharada. "Metal-Free Regioselective Dual C-H Functionalization in a Cascade Fashion: Access to Isocryptolepine Alkaloid Analogues". ChemistrySelect 2, n.º 12 (24 de abril de 2017): 3511–15. http://dx.doi.org/10.1002/slct.201700263.
Texto completoHåheim, Katja S., Emil Lindbäck, Kah Ni Tan, Marte Albrigtsen, Ida T. Urdal Helgeland, Clémence Lauga, Théodora Matringe et al. "Synthesis and Evaluation of the Tetracyclic Ring-System of Isocryptolepine and Regioisomers for Antimalarial, Antiproliferative and Antimicrobial Activities". Molecules 26, n.º 11 (30 de mayo de 2021): 3268. http://dx.doi.org/10.3390/molecules26113268.
Texto completoHayashi, Kaori, Tominari Choshi, Kyoko Chikaraishi, Aimi Oda, Rikako Yoshinaga, Noriyuki Hatae, Minoru Ishikura y Satoshi Hibino. "A novel total synthesis of isocryptolepine based on a microwave-assisted tandem Curtius rearrangement and aza-electrocyclic reaction". Tetrahedron 68, n.º 22 (junio de 2012): 4274–79. http://dx.doi.org/10.1016/j.tet.2012.03.055.
Texto completoHåheim, Katja S., Ida T. Urdal Helgeland, Emil Lindbäck y Magne O. Sydnes. "Mapping the reactivity of the quinoline ring-system – Synthesis of the tetracyclic ring-system of isocryptolepine and regioisomers". Tetrahedron 75, n.º 21 (mayo de 2019): 2949–57. http://dx.doi.org/10.1016/j.tet.2019.04.026.
Texto completoHingane, Dattatray G. y Radhika S. Kusurkar. "An efficient new route towards biologically active isocryptolepine and γ-carboline derivatives using an intramolecular thermal electrocyclization strategy". Tetrahedron Letters 52, n.º 28 (julio de 2011): 3686–88. http://dx.doi.org/10.1016/j.tetlet.2011.05.049.
Texto completoChen, Chen, Yuebo Wang, Xiaonan Shi, Wan Sun, Jinghui Zhao, Yan-Ping Zhu, Liying Liu y Bolin Zhu. "Palladium-Catalyzed C-2 and C-3 Dual C–H Functionalization of Indoles: Synthesis of Fluorinated Isocryptolepine Analogues". Organic Letters 22, n.º 11 (27 de mayo de 2020): 4097–102. http://dx.doi.org/10.1021/acs.orglett.0c01159.
Texto completoUchuskin, Maxim G., Arkady S. Pilipenko, Olga V. Serdyuk, Igor V. Trushkov y Alexander V. Butin. "From biomass to medicines. A simple synthesis of indolo[3,2-c]quinolines, antimalarial alkaloid isocryptolepine, and its derivatives". Organic & Biomolecular Chemistry 10, n.º 36 (2012): 7262. http://dx.doi.org/10.1039/c2ob25836f.
Texto completoChen, Xuebing, Peng Sun, Jinyi Xu, Xiaoming Wu, Lingyi Kong, Hequan Yao y Aijun Lin. "Construction of indoloquinolinones via Pd(II)-catalyzed tandem CC/CN bond formation: application to the total synthesis of isocryptolepine". Tetrahedron Letters 55, n.º 51 (diciembre de 2014): 7114–17. http://dx.doi.org/10.1016/j.tetlet.2014.11.008.
Texto completoHostyn, Steven, Bert U. W. Maes, Luc Pieters, Guy L. F. Lemière, Péter Mátyus, György Hajós y Roger A. Dommisse. "Synthesis of the benzo-β-carboline isoneocryptolepine: the missing indoloquinoline isomer in the alkaloid series cryptolepine, neocryptolepine and isocryptolepine". Tetrahedron 61, n.º 6 (febrero de 2005): 1571–77. http://dx.doi.org/10.1016/j.tet.2004.11.073.
Texto completoAgarwal, Piyush K., Devesh Sawant, Sunil Sharma y Bijoy Kundu. "New Route to the Synthesis of the Isocryptolepine Alkaloid and Its Related Skeletons Using a Modified Pictet-Spengler Reaction". European Journal of Organic Chemistry 2009, n.º 2 (enero de 2009): 292–303. http://dx.doi.org/10.1002/ejoc.200800929.
Texto completoMahajan, Pankaj S., Vivek T. Humne, Subhash D. Tanpure y Santosh B. Mhaske. "Radical Beckmann Rearrangement and Its Application in the Formal Total Synthesis of Antimalarial Natural Product Isocryptolepine via C–H Activation". Organic Letters 18, n.º 14 (5 de julio de 2016): 3450–53. http://dx.doi.org/10.1021/acs.orglett.6b01634.
Texto completoAksenov, Nicolai A., Alexander V. Aksenov, Alexander Kornienko, Annelise De Carvalho, Véronique Mathieu, Dmitrii A. Aksenov, Sergei N. Ovcharov, Georgii D. Griaznov y Michael Rubin. "A nitroalkane-based approach to one-pot three-component synthesis of isocryptolepine and its analogs with potent anti-cancer activities". RSC Advances 8, n.º 64 (2018): 36980–86. http://dx.doi.org/10.1039/c8ra08155g.
Texto completoIndu, Satrajit, Parthasarathi Subramanian y Krishna P. Kaliappan. "Transition-Metal-Catalyzed Selective Cyclization Strategy to 2-Substituted Benzofurans and Indoles en Route to the Oxa Analogues of Isocryptolepine". European Journal of Organic Chemistry 2014, n.º 32 (29 de septiembre de 2014): 7193–202. http://dx.doi.org/10.1002/ejoc.201402869.
Texto completoUchuskin, Maxim G., Arkady S. Pilipenko, Olga V. Serdyuk, Igor V. Trushkov y Alexander V. Butin. "ChemInform Abstract: From Biomass to Medicines. A Simple Synthesis of Indolo[3,2-c]quinolines, Antimalarial Alkaloid Isocryptolepine, and Its Derivatives." ChemInform 44, n.º 8 (19 de febrero de 2013): no. http://dx.doi.org/10.1002/chin.201308150.
Texto completoIndu, Satrajit, Parthasarathi Subramanian y Krishna P. Kaliappan. "ChemInform Abstract: Transition-Metal-Catalyzed Selective Cyclization Strategy to 2-Substituted Benzofurans and Indoles en Route to the Oxa Analogues of Isocryptolepine." ChemInform 46, n.º 16 (abril de 2015): no. http://dx.doi.org/10.1002/chin.201516147.
Texto completoChen, Xuebing, Peng Sun, Jinyi Xu, Xiaoming Wu, Lingyi Kong, Hequan Yao y Aijun Lin. "ChemInform Abstract: Construction of Indoloquinolinones via Pd(II)-Catalyzed Tandem C-C/C-N Bond Formation: Application to the Total Synthesis of Isocryptolepine." ChemInform 46, n.º 18 (16 de abril de 2015): no. http://dx.doi.org/10.1002/chin.201518218.
Texto completoWang, Ning, Kathryn J. Wicht, Kento Imai, Ming-qi Wang, Tran Anh Ngoc, Ryo Kiguchi, Marcel Kaiser, Timothy J. Egan y Tsutomu Inokuchi. "Synthesis, β-haematin inhibition, and in vitro antimalarial testing of isocryptolepine analogues: SAR study of indolo[3,2-c]quinolines with various substituents at C2, C6, and N11". Bioorganic & Medicinal Chemistry 22, n.º 9 (mayo de 2014): 2629–42. http://dx.doi.org/10.1016/j.bmc.2014.03.030.
Texto completoKirsch, Gilbert, Eslam El-Sawy y Ahmed Abdelwahab. "Utilization of 1H-Indole-3-carboxaldehyde as a Precursor for the Synthesis of Bioactive Indole Alkaloids". Synthesis 50, n.º 23 (15 de octubre de 2018): 4525–38. http://dx.doi.org/10.1055/s-0037-1610288.
Texto completoSchendera, Eva, Lisa‐Natascha Unkel, Phung Phan Huyen Quyen, Gwen Salkewitz, Frank Hoffmann, Alexander Villinger y Malte Brasholz. "Visible‐Light‐Mediated Aerobic Tandem Dehydrogenative Povarov/Aromatization Reaction: Synthesis of Isocryptolepines". Chemistry – A European Journal 26, n.º 1 (27 de noviembre de 2019): 269–74. http://dx.doi.org/10.1002/chem.201903921.
Texto completoJonckers, Tim H. M., Bert U. W. Maes, Guy L. F. Lemiere, Geert Rombouts, Luc Pieters, Achiel Haemers y Roger A. Dommisse. "Synthesis of Isocryptolepine via a Pd-Catalyzed “Amination—Arylation” Approach." ChemInform 34, n.º 30 (29 de julio de 2003). http://dx.doi.org/10.1002/chin.200330227.
Texto completoMorozov, Vyacheslav y Yurii Shklyaev. "Metal‐Free Rapid Diastereoselective Construction of Isocryptolepine Core via Elecrophilic Dearomatization ‐ Inramolecular Michael Addition Sequence". ChemistrySelect 7, n.º 23 (14 de junio de 2022). http://dx.doi.org/10.1002/slct.202201709.
Texto completoHostyn, Steven, Bert U. W. Maes, Luc Pieters, Guy L. F. Lemiere, Peter Matyus, Gyoergy Hajos y Roger A. Dommisse. "Synthesis of the Benzo-β-Carboline Isoneocryptolepine: The Missing Indoloquinoline Isomer in the Alkaloid Series Cryptolepine, Neocryptolepine and Isocryptolepine." ChemInform 36, n.º 23 (7 de junio de 2005). http://dx.doi.org/10.1002/chin.200523212.
Texto completoAgarwal, Piyush K., Devesh Sawant, Sunil Sharma y Bijoy Kundu. "ChemInform Abstract: New Route to the Synthesis of the Isocryptolepine Alkaloid and Its Related Skeletons Using a Modified Pictet-Spengler Reaction." ChemInform 40, n.º 20 (19 de mayo de 2009). http://dx.doi.org/10.1002/chin.200920188.
Texto completoMahajan, Pankaj S., Vivek T. Humne, Subhash D. Tanpure y Santosh B. Mhaske. "ChemInform Abstract: Radical Beckmann Rearrangement and Its Application in the Formal Total Synthesis of Antimalarial Natural Product Isocryptolepine via C-H Activation." ChemInform 47, n.º 48 (noviembre de 2016). http://dx.doi.org/10.1002/chin.201648028.
Texto completoVerma, Kanchan, Yogesh Kumar Tailor, Sarita Khandelwal, Monu Agarwal, Esha Rushell, Sakshi Pathak, Yogita Kumari, Kamlendra Awasthi y Mahendra Kumar. "Synthesis and characterization of terbium doped TiO 2 nanoparticles and their use as recyclable and reusable heterogeneous catalyst for efficient and environmentally sustainable synthesis of spiroannulated indolo[3,2‐ c ]quinolines‐ mimetic scaffolds of isocryptolepine". Applied Organometallic Chemistry 34, n.º 10 (8 de junio de 2020). http://dx.doi.org/10.1002/aoc.5836.
Texto completo