Artículos de revistas sobre el tema "Indoles"
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Sharma, Upendra, Inder Kumar y Rakesh Kumar. "Recent Advances in the Regioselective Synthesis of Indoles via C–H Activation/Functionalization". Synthesis 50, n.º 14 (28 de mayo de 2018): 2655–77. http://dx.doi.org/10.1055/s-0037-1609733.
Texto completoVincent, Guillaume, Hussein Abou-Hamdan y Cyrille Kouklovsky. "Dearomatization Reactions of Indoles to Access 3D Indoline Structures". Synlett 31, n.º 18 (24 de junio de 2020): 1775–88. http://dx.doi.org/10.1055/s-0040-1707152.
Texto completoKumar, Anil y Ganesh Shelke. "Sc(OTf)3-Catalyzed Oligomerization of Indole: One-Pot Synthesis of 2-[2,2-Bis(indol-3-yl)ethyl]anilines and 3-(Indolin-2-yl)indoles". Synthesis 49, n.º 18 (1 de agosto de 2017): 4321–26. http://dx.doi.org/10.1055/s-0036-1588181.
Texto completoTrubitsõn, Dmitri y Tõnis Kanger. "Enantioselective Catalytic Synthesis of N-alkylated Indoles". Symmetry 12, n.º 7 (17 de julio de 2020): 1184. http://dx.doi.org/10.3390/sym12071184.
Texto completoFang, Xinxin, Shang Gao, Zijun Wu, Hequan Yao y Aijun Lin. "Pd(ii)-Catalyzed oxidative dearomatization of indoles: substrate-controlled synthesis of indolines and indolones". Organic Chemistry Frontiers 4, n.º 2 (2017): 292–96. http://dx.doi.org/10.1039/c6qo00698a.
Texto completoLi, Jiao y Chun-Lin Zhuang. "Natural Indole Alkaloids from Marine Fungi: Chemical Diversity and Biological Activities". Pharmaceutical Fronts 03, n.º 04 (diciembre de 2021): e139-e163. http://dx.doi.org/10.1055/s-0041-1740050.
Texto completoAshram, Muhammad, Ahmed Al-Mustafa, Wael A. Al-Zereini, Firas F. Awwadi y Islam Ashram. "A convenient one-pot approach to the synthesis of novel pyrazino[1,2-a]indoles fused to heterocyclic systems and evaluation of their biological activity as acetylcholinesterase inhibitors". Zeitschrift für Naturforschung B 76, n.º 5 (1 de mayo de 2021): 303–12. http://dx.doi.org/10.1515/znb-2020-0205.
Texto completoYan, Jianwei, Guangjie He, Fulin Yan, Jixia Zhang y Guisheng Zhang. "The dicarbonylation of indoles via Friedel–Crafts reaction with dicarbonyl nitrile generated in situ and retro-cyanohydrination". RSC Advances 6, n.º 50 (2016): 44029–33. http://dx.doi.org/10.1039/c6ra04016k.
Texto completoSharapov, Ainur D., Ramil F. Fatykhov, Igor A. Khalymbadzha, Maria I. Valieva, Igor L. Nikonov, Olga S. Taniya, Dmitry S. Kopchuk et al. "Fluorescent Pyranoindole Congeners: Synthesis and Photophysical Properties of Pyrano[3,2-f], [2,3-g], [2,3-f], and [2,3-e]Indoles". Molecules 27, n.º 24 (13 de diciembre de 2022): 8867. http://dx.doi.org/10.3390/molecules27248867.
Texto completoHazra, Somjit, Biplab Mondal, Rajendra Narayan De y Brindaban Roy. "Pd-catalyzed dehydrogenative C–H activation of iminyl hydrogen with the indole C3–H and C2–H bond: an elegant synthesis of indeno[1,2-b]indoles and indolo[1,2-a]indoles". RSC Advances 5, n.º 29 (2015): 22480–89. http://dx.doi.org/10.1039/c4ra16661b.
Texto completoDas, Jonali y Sajal Kumar Das. "Regioselectivity of the SEAr-based cyclizations and SEAr-terminated annulations of 3,5-unsubstituted, 4-substituted indoles". Beilstein Journal of Organic Chemistry 18 (8 de marzo de 2022): 293–302. http://dx.doi.org/10.3762/bjoc.18.33.
Texto completoZeng, Ming, Jiaqi Chen, Fengye Li, Haojie Li, Lan Zhao, Dengzhao Jiang, Jun Dai y Wenbo Liu. "Ruthenium-Catalyzed Oxidative Synthesis of N-(2-triazine)indoles by C-H Activation". Molecules 28, n.º 9 (24 de abril de 2023): 3676. http://dx.doi.org/10.3390/molecules28093676.
Texto completoTanaka, Yosuke, Takumi Ikeda, Yasuhiro Nachi, Taisei Mizuno, Kousuke Maeda, Chisato Sakamoto, Mugen Yamawaki, Toshio Morita y Yasuharu Yoshimi. "Transition-Metal-Free Access to 2-Subsituted Indolines from Indoles via Dearomative Nucleophilic Addition Using Two-Molecule Organic Photoredox Catalysts". Photochem 1, n.º 3 (1 de noviembre de 2021): 448–57. http://dx.doi.org/10.3390/photochem1030027.
Texto completoZhu, Haoran, Sen Zhao, Yu Zhou, Chunpu Li y Hong Liu. "Ruthenium-Catalyzed C–H Activations for the Synthesis of Indole Derivatives". Catalysts 10, n.º 11 (29 de octubre de 2020): 1253. http://dx.doi.org/10.3390/catal10111253.
Texto completoWu, Shang, Quanlu Yang, Qinzheng Hu, Yanbin Wang, Lihua Chen, Hong Zhang, Lan Wu y Jia Li. "Manganese-catalyzed direct C2-allylation of indoles". Organic Chemistry Frontiers 5, n.º 19 (2018): 2852–55. http://dx.doi.org/10.1039/c8qo00674a.
Texto completoSun, Haoyi, Kangping Sun y Jingyong Sun. "Recent Advances of Marine Natural Indole Products in Chemical and Biological Aspects". Molecules 28, n.º 5 (27 de febrero de 2023): 2204. http://dx.doi.org/10.3390/molecules28052204.
Texto completoPowell, Domonica N., Alyson Swimm, Robert Sonowal, Alexis Bretin, Andrew T. Gewirtz, Rheinallt M. Jones y Daniel Kalman. "Indoles from the commensal microbiota act via the AHR and IL-10 to tune the cellular composition of the colonic epithelium during aging". Proceedings of the National Academy of Sciences 117, n.º 35 (17 de agosto de 2020): 21519–26. http://dx.doi.org/10.1073/pnas.2003004117.
Texto completoSarkar, Deeptanu, Andleeb Amin, Tanzeela Qadir y Praveen K. Sharma. "Synthesis of Medicinally Important Indole Derivatives: A Review". Open Medicinal Chemistry Journal 15, n.º 1 (30 de septiembre de 2021): 1–16. http://dx.doi.org/10.2174/1874104502015010001.
Texto completoGribble, G. W. "Novel chemistry of indole in the synthesis of heterocycles". Pure and Applied Chemistry 75, n.º 10 (1 de enero de 2003): 1417–32. http://dx.doi.org/10.1351/pac200375101417.
Texto completoYan, Xue, Ying-De Tang, Cheng-Shi Jiang, Xigong Liu y Hua Zhang. "Oxidative Dearomative Cross-Dehydrogenative Coupling of Indoles with Diverse C-H Nucleophiles: Efficient Approach to 2,2-Disubstituted Indolin-3-ones". Molecules 25, n.º 2 (20 de enero de 2020): 419. http://dx.doi.org/10.3390/molecules25020419.
Texto completoHaak, Edgar. "Modern Annulation Strategies for the Synthesis of Cyclo[b]fused Indoles". Synlett 30, n.º 03 (13 de diciembre de 2018): 245–51. http://dx.doi.org/10.1055/s-0037-1610336.
Texto completoAbdel-Hay, Karim M., Tarek S. Belal, Younis Abiedalla, Amber Thaxton-Weissenfluh, Jack DeRuiter, Forrest Smith y C. Randall Clark. "Gas Chromatography–Mass Spectrometry (GC–MS) and Gas Chromatography–Infrared (GC–IR) Analyses of the Chloro-1-n-pentyl-3-(1-naphthoyl)-Indoles: Regioisomeric Cannabinoids". Applied Spectroscopy 73, n.º 4 (16 de noviembre de 2018): 433–43. http://dx.doi.org/10.1177/0003702818809998.
Texto completoZhang, Yan, Zhe-Yao Hu, Xin-Chang Li y Xun-Xiang Guo. "Copper-Catalyzed Decarboxylative N-Arylation of Indole-2-carboxylic Acids". Synthesis 51, n.º 08 (10 de enero de 2019): 1803–8. http://dx.doi.org/10.1055/s-0037-1611946.
Texto completoZgarbová, Eliška y Radim Vrzal. "The Impact of Indoles Activating the Aryl Hydrocarbon Receptor on Androgen Receptor Activity in the 22Rv1 Prostate Cancer Cell Line". International Journal of Molecular Sciences 24, n.º 1 (28 de diciembre de 2022): 502. http://dx.doi.org/10.3390/ijms24010502.
Texto completoSingh, Anoop, Satheeshvarma Vanaparthi, Sachin Choudhary, Rangan Krishnan y Indresh Kumar. "Synthesis of C2-tetrasubstituted indolin-3-ones via Cu-catalyzed oxidative dimerization of 2-aryl indoles and cross-addition with indoles". RSC Advances 9, n.º 42 (2019): 24050–56. http://dx.doi.org/10.1039/c9ra04741g.
Texto completoMazzotta, Sarah, Luca Frattaruolo, Matteo Brindisi, Cristina Ulivieri, Francesca Vanni, Antonella Brizzi, Gabriele Carullo, Anna R. Cappello y Francesca Aiello. "3-Amino-alkylated indoles: unexplored green products acting as anti-inflammatory agents". Future Medicinal Chemistry 12, n.º 1 (enero de 2020): 5–17. http://dx.doi.org/10.4155/fmc-2019-0234.
Texto completoFang, Shu-Yen, Sheng-Yuan Chen, You-Ying Chen, Tsu-Jen Kuo, Zhi-Hong Wen, Yu-Hsin Chen, Tsong-Long Hwang y Ping-Jyun Sung. "Natural Indoles From the Bacterium Pseudovibrio denitrificans P81 Isolated From a Marine Sponge, Aaptos Species". Natural Product Communications 16, n.º 9 (septiembre de 2021): 1934578X2110337. http://dx.doi.org/10.1177/1934578x211033735.
Texto completoChen, Xiao Yun, Yaonan Tang, Xinran Xiang, Yisong Tang, Mingyang Huang, Shaojun Zheng y Cuifeng Yang. "Green One-Pot Syntheses of 2-Sulfoximidoyl-3,6-Dibromo Indoles Using N-Br Sulfoximines as Both Brominating and Sulfoximinating Reagents". Molecules 28, n.º 8 (11 de abril de 2023): 3380. http://dx.doi.org/10.3390/molecules28083380.
Texto completoSarath Chand, S., B. S. Sasidhar, Praveen Prakash, P. Sasikumar, P. Preethanuj, Florian Jaroschik, Dominique Harakat, Jean-Luc Vasse y K. V. Radhakrishnan. "Lewis acid catalyzed C-3 alkylidenecyclopentenylation of indoles: an easy access to functionalized indoles and bisindoles". RSC Advances 5, n.º 48 (2015): 38075–84. http://dx.doi.org/10.1039/c5ra01107h.
Texto completoShen, Yang, Zi-Qi Zhu, Jin-Xi Liu, Lei Yu, Bai-Xiang Du, Guang-Jian Mei y Feng Shi. "Brønsted Acid Catalyzed C3-Alkylation of 2-Indolylmethanols with Azlactones via an Umpolung Strategy". Synthesis 49, n.º 17 (20 de junio de 2017): 4025–34. http://dx.doi.org/10.1055/s-0036-1589036.
Texto completoFochi, Mariafrancesca, Luca Bernardi y Lorenzo Caruana. "Enantioselective Approaches to 3,4-Annulated Indoles Using Organocatalytic Domino Reactions". Synlett 28, n.º 13 (19 de abril de 2017): 1530–43. http://dx.doi.org/10.1055/s-0036-1589494.
Texto completoMartínez, Gabriela, Oscar E. Zimerman y Norman A. García. "The Aerobic Riboflavin-Sensitized Photodecomposition of Tryptophan, Tryptamine and Indole Acetic Acid. Ground-State and Photopromoted Flavin-Indole Interactions". Collection of Czechoslovak Chemical Communications 58, n.º 6 (1993): 1299–308. http://dx.doi.org/10.1135/cccc19931299.
Texto completoKhan, Neyaz A., Navdeep Kaur, Peter Owens, Olivier P. Thomas y Aoife Boyd. "Bis-Indole Alkaloids Isolated from the Sponge Spongosorites calcicola Disrupt Cell Membranes of MRSA". International Journal of Molecular Sciences 23, n.º 4 (11 de febrero de 2022): 1991. http://dx.doi.org/10.3390/ijms23041991.
Texto completoHilgeroth, Andreas, Kaveh Yasrebi, Sibel Suzen, Tobias Hertlein, Knut Ohlsen y Michael Lalk. "Antibacterial Evaluation of Novel Substituted Cycloheptaindoles in Staphylococcus and Enterococcus Strains". Medicinal Chemistry 15, n.º 8 (18 de noviembre de 2019): 833–39. http://dx.doi.org/10.2174/1573406415666190208170126.
Texto completoRinderspacher, Alison y Gordon W. Gribble. "The Generation of Indole-2,3-quinodimethanes from the Deamination of 1,2,3,4-Tetrahydropyrrolo[3,4-b]indoles". Molecules 25, n.º 2 (9 de enero de 2020): 261. http://dx.doi.org/10.3390/molecules25020261.
Texto completoBartoli, Giuseppe, Renato Dalpozzo y Monica Nardi. "Applications of Bartoli indole synthesis". Chem. Soc. Rev. 43, n.º 13 (2014): 4728–50. http://dx.doi.org/10.1039/c4cs00045e.
Texto completoNi, Penghui, Bin Li, Huawen Huang, Fuhong Xiao y Guo-Jun Deng. "Solvent-controlled highly regio-selective thieno[2,3-b]indole formation under metal-free conditions". Green Chemistry 19, n.º 23 (2017): 5553–58. http://dx.doi.org/10.1039/c7gc02818k.
Texto completoLiu, Jiarun, Jiancheng Huang, Kuiyong Jia, Tianxing Du, Changyin Zhao, Rongxiu Zhu y Xigong Liu. "Direct Oxidative Dearomatization of Indoles with Aromatic Ketones: Rapid Access to 2,2-Disubstituted Indolin-3-ones". Synthesis 52, n.º 05 (28 de noviembre de 2019): 763–68. http://dx.doi.org/10.1055/s-0039-1691528.
Texto completoSun, Wei, William A. T. Raimbach, Luke D. Elliott, Kevin I. Booker-Milburn y David C. Harrowven. "New approaches to ondansetron and alosetron inspire a versatile, flow photochemical method for indole synthesis". Chemical Communications 58, n.º 3 (2022): 383–86. http://dx.doi.org/10.1039/d1cc05700f.
Texto completoSanap, Anita Kailas y Ganapati Subray Shankarling. "Choline chloride based eutectic solvents: direct C-3 alkenylation/alkylation of indoles with 1,3-dicarbonyl compounds". RSC Adv. 4, n.º 66 (2014): 34938–43. http://dx.doi.org/10.1039/c4ra05858e.
Texto completoPadmaja, Pannala, Pedavenkatagari Narayana Reddy y Bijaya Ketan Sahoo. "A Green Approach to the Synthesis of Novel Indole Substituted 2-Amino- 4,5-dihydro-3-furancarbonitriles in Water". Letters in Organic Chemistry 16, n.º 3 (11 de febrero de 2019): 209–14. http://dx.doi.org/10.2174/1570178615666180917104820.
Texto completoSonowal, Robert, Alyson Swimm, Anusmita Sahoo, Liping Luo, Yohei Matsunaga, Ziqi Wu, Jui A. Bhingarde et al. "Indoles from commensal bacteria extend healthspan". Proceedings of the National Academy of Sciences 114, n.º 36 (21 de agosto de 2017): E7506—E7515. http://dx.doi.org/10.1073/pnas.1706464114.
Texto completoAksenov, Nicolai A., Nikolai A. Arutiunov, Igor A. Kurenkov, Vladimir V. Malyuga, Dmitrii A. Aksenov, Daria S. Momotova, Anna M. Zatsepilina, Elizaveta A. Chukanova, Alexander V. Leontiev y Alexander V. Aksenov. "A Two-Step Synthesis of Unprotected 3-Aminoindoles via Post Functionalization with Nitrostyrene". Molecules 28, n.º 9 (23 de abril de 2023): 3657. http://dx.doi.org/10.3390/molecules28093657.
Texto completoYuan, Hao, Jianxian Gong y Zhen Yang. "A rhodium-catalyzed tandem reaction of N-sulfonyl triazoles with indoles: access to indole-substituted indanones". Chemical Communications 53, n.º 65 (2017): 9089–92. http://dx.doi.org/10.1039/c7cc05139e.
Texto completoZhang, Yong-Sheng, Xiang-Ying Tang y Min Shi. "Divergent synthesis of indole-fused polycycles via Rh(ii)-catalyzed intramolecular [3 + 2] cycloaddition and C–H functionalization of indolyltriazoles". Organic Chemistry Frontiers 2, n.º 11 (2015): 1516–20. http://dx.doi.org/10.1039/c5qo00216h.
Texto completoZalte, Rajesh R., Alexey A. Festa, Nikita E. Golantsov, Karthikeyan Subramani, Victor B. Rybakov, Alexey V. Varlamov, Rafael Luque y Leonid G. Voskressensky. "Aza-Henry and aza-Knoevenagel reactions of nitriles for the synthesis of pyrido[1,2-a]indoles". Chemical Communications 56, n.º 48 (2020): 6527–30. http://dx.doi.org/10.1039/d0cc01652g.
Texto completoBakthadoss, Manickam, Polu Vijay Kumar, Tadiparthi Thirupathi Reddy y Duddu S. Sharada. "Solvent and catalyst free ring expansion of indoles: a simple synthesis of highly functionalized benzazepines". Organic & Biomolecular Chemistry 16, n.º 43 (2018): 8160–68. http://dx.doi.org/10.1039/c8ob01825a.
Texto completoEldehna, Wagdy M., Ghada S. Hassan, Sara T. Al-Rashood, Hamad M. Alkahtani, Abdulrahman A. Almehizia y Ghada H. Al-Ansary. "Marine-Inspired Bis-indoles Possessing Antiproliferative Activity against Breast Cancer; Design, Synthesis, and Biological Evaluation". Marine Drugs 18, n.º 4 (2 de abril de 2020): 190. http://dx.doi.org/10.3390/md18040190.
Texto completoUruvakili, Anasuyamma y K. C. Kumara Swamy. "Gold catalysed transformation of 2-arylindoles to terphenyl amines via 3-dienyl indoles and Brønsted acid promoted formation of 2-carboxyindoles to 3-indenylindoles via 3-allenylindoles". Organic & Biomolecular Chemistry 17, n.º 12 (2019): 3275–84. http://dx.doi.org/10.1039/c9ob00232d.
Texto completoMacha, Lingamurthy, Deepak Singh, Hyong-Jin Rhee y Hyun-Joon Ha. "Lewis acid-mediated synthesis of mono- and tris-indole adducts from chiral aziridines". Organic & Biomolecular Chemistry 18, n.º 46 (2020): 9473–82. http://dx.doi.org/10.1039/d0ob01865a.
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