Artykuły w czasopismach na temat „Indoles”
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Sharma, Upendra, Inder Kumar i Rakesh Kumar. "Recent Advances in the Regioselective Synthesis of Indoles via C–H Activation/Functionalization". Synthesis 50, nr 14 (28.05.2018): 2655–77. http://dx.doi.org/10.1055/s-0037-1609733.
Pełny tekst źródłaVincent, Guillaume, Hussein Abou-Hamdan i Cyrille Kouklovsky. "Dearomatization Reactions of Indoles to Access 3D Indoline Structures". Synlett 31, nr 18 (24.06.2020): 1775–88. http://dx.doi.org/10.1055/s-0040-1707152.
Pełny tekst źródłaKumar, Anil, i 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, nr 18 (1.08.2017): 4321–26. http://dx.doi.org/10.1055/s-0036-1588181.
Pełny tekst źródłaTrubitsõn, Dmitri, i Tõnis Kanger. "Enantioselective Catalytic Synthesis of N-alkylated Indoles". Symmetry 12, nr 7 (17.07.2020): 1184. http://dx.doi.org/10.3390/sym12071184.
Pełny tekst źródłaFang, Xinxin, Shang Gao, Zijun Wu, Hequan Yao i Aijun Lin. "Pd(ii)-Catalyzed oxidative dearomatization of indoles: substrate-controlled synthesis of indolines and indolones". Organic Chemistry Frontiers 4, nr 2 (2017): 292–96. http://dx.doi.org/10.1039/c6qo00698a.
Pełny tekst źródłaLi, Jiao, i Chun-Lin Zhuang. "Natural Indole Alkaloids from Marine Fungi: Chemical Diversity and Biological Activities". Pharmaceutical Fronts 03, nr 04 (grudzień 2021): e139-e163. http://dx.doi.org/10.1055/s-0041-1740050.
Pełny tekst źródłaAshram, Muhammad, Ahmed Al-Mustafa, Wael A. Al-Zereini, Firas F. Awwadi i 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, nr 5 (1.05.2021): 303–12. http://dx.doi.org/10.1515/znb-2020-0205.
Pełny tekst źródłaYan, Jianwei, Guangjie He, Fulin Yan, Jixia Zhang i Guisheng Zhang. "The dicarbonylation of indoles via Friedel–Crafts reaction with dicarbonyl nitrile generated in situ and retro-cyanohydrination". RSC Advances 6, nr 50 (2016): 44029–33. http://dx.doi.org/10.1039/c6ra04016k.
Pełny tekst źródłaSharapov, Ainur D., Ramil F. Fatykhov, Igor A. Khalymbadzha, Maria I. Valieva, Igor L. Nikonov, Olga S. Taniya, Dmitry S. Kopchuk i in. "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, nr 24 (13.12.2022): 8867. http://dx.doi.org/10.3390/molecules27248867.
Pełny tekst źródłaHazra, Somjit, Biplab Mondal, Rajendra Narayan De i 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, nr 29 (2015): 22480–89. http://dx.doi.org/10.1039/c4ra16661b.
Pełny tekst źródłaDas, Jonali, i 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 (8.03.2022): 293–302. http://dx.doi.org/10.3762/bjoc.18.33.
Pełny tekst źródłaZeng, Ming, Jiaqi Chen, Fengye Li, Haojie Li, Lan Zhao, Dengzhao Jiang, Jun Dai i Wenbo Liu. "Ruthenium-Catalyzed Oxidative Synthesis of N-(2-triazine)indoles by C-H Activation". Molecules 28, nr 9 (24.04.2023): 3676. http://dx.doi.org/10.3390/molecules28093676.
Pełny tekst źródłaTanaka, Yosuke, Takumi Ikeda, Yasuhiro Nachi, Taisei Mizuno, Kousuke Maeda, Chisato Sakamoto, Mugen Yamawaki, Toshio Morita i Yasuharu Yoshimi. "Transition-Metal-Free Access to 2-Subsituted Indolines from Indoles via Dearomative Nucleophilic Addition Using Two-Molecule Organic Photoredox Catalysts". Photochem 1, nr 3 (1.11.2021): 448–57. http://dx.doi.org/10.3390/photochem1030027.
Pełny tekst źródłaZhu, Haoran, Sen Zhao, Yu Zhou, Chunpu Li i Hong Liu. "Ruthenium-Catalyzed C–H Activations for the Synthesis of Indole Derivatives". Catalysts 10, nr 11 (29.10.2020): 1253. http://dx.doi.org/10.3390/catal10111253.
Pełny tekst źródłaWu, Shang, Quanlu Yang, Qinzheng Hu, Yanbin Wang, Lihua Chen, Hong Zhang, Lan Wu i Jia Li. "Manganese-catalyzed direct C2-allylation of indoles". Organic Chemistry Frontiers 5, nr 19 (2018): 2852–55. http://dx.doi.org/10.1039/c8qo00674a.
Pełny tekst źródłaSun, Haoyi, Kangping Sun i Jingyong Sun. "Recent Advances of Marine Natural Indole Products in Chemical and Biological Aspects". Molecules 28, nr 5 (27.02.2023): 2204. http://dx.doi.org/10.3390/molecules28052204.
Pełny tekst źródłaPowell, Domonica N., Alyson Swimm, Robert Sonowal, Alexis Bretin, Andrew T. Gewirtz, Rheinallt M. Jones i 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, nr 35 (17.08.2020): 21519–26. http://dx.doi.org/10.1073/pnas.2003004117.
Pełny tekst źródłaSarkar, Deeptanu, Andleeb Amin, Tanzeela Qadir i Praveen K. Sharma. "Synthesis of Medicinally Important Indole Derivatives: A Review". Open Medicinal Chemistry Journal 15, nr 1 (30.09.2021): 1–16. http://dx.doi.org/10.2174/1874104502015010001.
Pełny tekst źródłaGribble, G. W. "Novel chemistry of indole in the synthesis of heterocycles". Pure and Applied Chemistry 75, nr 10 (1.01.2003): 1417–32. http://dx.doi.org/10.1351/pac200375101417.
Pełny tekst źródłaYan, Xue, Ying-De Tang, Cheng-Shi Jiang, Xigong Liu i 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, nr 2 (20.01.2020): 419. http://dx.doi.org/10.3390/molecules25020419.
Pełny tekst źródłaHaak, Edgar. "Modern Annulation Strategies for the Synthesis of Cyclo[b]fused Indoles". Synlett 30, nr 03 (13.12.2018): 245–51. http://dx.doi.org/10.1055/s-0037-1610336.
Pełny tekst źródłaAbdel-Hay, Karim M., Tarek S. Belal, Younis Abiedalla, Amber Thaxton-Weissenfluh, Jack DeRuiter, Forrest Smith i 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, nr 4 (16.11.2018): 433–43. http://dx.doi.org/10.1177/0003702818809998.
Pełny tekst źródłaZhang, Yan, Zhe-Yao Hu, Xin-Chang Li i Xun-Xiang Guo. "Copper-Catalyzed Decarboxylative N-Arylation of Indole-2-carboxylic Acids". Synthesis 51, nr 08 (10.01.2019): 1803–8. http://dx.doi.org/10.1055/s-0037-1611946.
Pełny tekst źródłaZgarbová, Eliška, i 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, nr 1 (28.12.2022): 502. http://dx.doi.org/10.3390/ijms24010502.
Pełny tekst źródłaSingh, Anoop, Satheeshvarma Vanaparthi, Sachin Choudhary, Rangan Krishnan i 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, nr 42 (2019): 24050–56. http://dx.doi.org/10.1039/c9ra04741g.
Pełny tekst źródłaMazzotta, Sarah, Luca Frattaruolo, Matteo Brindisi, Cristina Ulivieri, Francesca Vanni, Antonella Brizzi, Gabriele Carullo, Anna R. Cappello i Francesca Aiello. "3-Amino-alkylated indoles: unexplored green products acting as anti-inflammatory agents". Future Medicinal Chemistry 12, nr 1 (styczeń 2020): 5–17. http://dx.doi.org/10.4155/fmc-2019-0234.
Pełny tekst źródłaFang, Shu-Yen, Sheng-Yuan Chen, You-Ying Chen, Tsu-Jen Kuo, Zhi-Hong Wen, Yu-Hsin Chen, Tsong-Long Hwang i Ping-Jyun Sung. "Natural Indoles From the Bacterium Pseudovibrio denitrificans P81 Isolated From a Marine Sponge, Aaptos Species". Natural Product Communications 16, nr 9 (wrzesień 2021): 1934578X2110337. http://dx.doi.org/10.1177/1934578x211033735.
Pełny tekst źródłaChen, Xiao Yun, Yaonan Tang, Xinran Xiang, Yisong Tang, Mingyang Huang, Shaojun Zheng i 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, nr 8 (11.04.2023): 3380. http://dx.doi.org/10.3390/molecules28083380.
Pełny tekst źródłaSarath Chand, S., B. S. Sasidhar, Praveen Prakash, P. Sasikumar, P. Preethanuj, Florian Jaroschik, Dominique Harakat, Jean-Luc Vasse i K. V. Radhakrishnan. "Lewis acid catalyzed C-3 alkylidenecyclopentenylation of indoles: an easy access to functionalized indoles and bisindoles". RSC Advances 5, nr 48 (2015): 38075–84. http://dx.doi.org/10.1039/c5ra01107h.
Pełny tekst źródłaShen, Yang, Zi-Qi Zhu, Jin-Xi Liu, Lei Yu, Bai-Xiang Du, Guang-Jian Mei i Feng Shi. "Brønsted Acid Catalyzed C3-Alkylation of 2-Indolylmethanols with Azlactones via an Umpolung Strategy". Synthesis 49, nr 17 (20.06.2017): 4025–34. http://dx.doi.org/10.1055/s-0036-1589036.
Pełny tekst źródłaFochi, Mariafrancesca, Luca Bernardi i Lorenzo Caruana. "Enantioselective Approaches to 3,4-Annulated Indoles Using Organocatalytic Domino Reactions". Synlett 28, nr 13 (19.04.2017): 1530–43. http://dx.doi.org/10.1055/s-0036-1589494.
Pełny tekst źródłaMartínez, Gabriela, Oscar E. Zimerman i 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, nr 6 (1993): 1299–308. http://dx.doi.org/10.1135/cccc19931299.
Pełny tekst źródłaKhan, Neyaz A., Navdeep Kaur, Peter Owens, Olivier P. Thomas i Aoife Boyd. "Bis-Indole Alkaloids Isolated from the Sponge Spongosorites calcicola Disrupt Cell Membranes of MRSA". International Journal of Molecular Sciences 23, nr 4 (11.02.2022): 1991. http://dx.doi.org/10.3390/ijms23041991.
Pełny tekst źródłaHilgeroth, Andreas, Kaveh Yasrebi, Sibel Suzen, Tobias Hertlein, Knut Ohlsen i Michael Lalk. "Antibacterial Evaluation of Novel Substituted Cycloheptaindoles in Staphylococcus and Enterococcus Strains". Medicinal Chemistry 15, nr 8 (18.11.2019): 833–39. http://dx.doi.org/10.2174/1573406415666190208170126.
Pełny tekst źródłaRinderspacher, Alison, i 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, nr 2 (9.01.2020): 261. http://dx.doi.org/10.3390/molecules25020261.
Pełny tekst źródłaBartoli, Giuseppe, Renato Dalpozzo i Monica Nardi. "Applications of Bartoli indole synthesis". Chem. Soc. Rev. 43, nr 13 (2014): 4728–50. http://dx.doi.org/10.1039/c4cs00045e.
Pełny tekst źródłaNi, Penghui, Bin Li, Huawen Huang, Fuhong Xiao i Guo-Jun Deng. "Solvent-controlled highly regio-selective thieno[2,3-b]indole formation under metal-free conditions". Green Chemistry 19, nr 23 (2017): 5553–58. http://dx.doi.org/10.1039/c7gc02818k.
Pełny tekst źródłaLiu, Jiarun, Jiancheng Huang, Kuiyong Jia, Tianxing Du, Changyin Zhao, Rongxiu Zhu i Xigong Liu. "Direct Oxidative Dearomatization of Indoles with Aromatic Ketones: Rapid Access to 2,2-Disubstituted Indolin-3-ones". Synthesis 52, nr 05 (28.11.2019): 763–68. http://dx.doi.org/10.1055/s-0039-1691528.
Pełny tekst źródłaSun, Wei, William A. T. Raimbach, Luke D. Elliott, Kevin I. Booker-Milburn i David C. Harrowven. "New approaches to ondansetron and alosetron inspire a versatile, flow photochemical method for indole synthesis". Chemical Communications 58, nr 3 (2022): 383–86. http://dx.doi.org/10.1039/d1cc05700f.
Pełny tekst źródłaSanap, Anita Kailas, i Ganapati Subray Shankarling. "Choline chloride based eutectic solvents: direct C-3 alkenylation/alkylation of indoles with 1,3-dicarbonyl compounds". RSC Adv. 4, nr 66 (2014): 34938–43. http://dx.doi.org/10.1039/c4ra05858e.
Pełny tekst źródłaPadmaja, Pannala, Pedavenkatagari Narayana Reddy i 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, nr 3 (11.02.2019): 209–14. http://dx.doi.org/10.2174/1570178615666180917104820.
Pełny tekst źródłaSonowal, Robert, Alyson Swimm, Anusmita Sahoo, Liping Luo, Yohei Matsunaga, Ziqi Wu, Jui A. Bhingarde i in. "Indoles from commensal bacteria extend healthspan". Proceedings of the National Academy of Sciences 114, nr 36 (21.08.2017): E7506—E7515. http://dx.doi.org/10.1073/pnas.1706464114.
Pełny tekst źródłaAksenov, 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 i Alexander V. Aksenov. "A Two-Step Synthesis of Unprotected 3-Aminoindoles via Post Functionalization with Nitrostyrene". Molecules 28, nr 9 (23.04.2023): 3657. http://dx.doi.org/10.3390/molecules28093657.
Pełny tekst źródłaYuan, Hao, Jianxian Gong i Zhen Yang. "A rhodium-catalyzed tandem reaction of N-sulfonyl triazoles with indoles: access to indole-substituted indanones". Chemical Communications 53, nr 65 (2017): 9089–92. http://dx.doi.org/10.1039/c7cc05139e.
Pełny tekst źródłaZhang, Yong-Sheng, Xiang-Ying Tang i 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, nr 11 (2015): 1516–20. http://dx.doi.org/10.1039/c5qo00216h.
Pełny tekst źródłaZalte, Rajesh R., Alexey A. Festa, Nikita E. Golantsov, Karthikeyan Subramani, Victor B. Rybakov, Alexey V. Varlamov, Rafael Luque i Leonid G. Voskressensky. "Aza-Henry and aza-Knoevenagel reactions of nitriles for the synthesis of pyrido[1,2-a]indoles". Chemical Communications 56, nr 48 (2020): 6527–30. http://dx.doi.org/10.1039/d0cc01652g.
Pełny tekst źródłaBakthadoss, Manickam, Polu Vijay Kumar, Tadiparthi Thirupathi Reddy i Duddu S. Sharada. "Solvent and catalyst free ring expansion of indoles: a simple synthesis of highly functionalized benzazepines". Organic & Biomolecular Chemistry 16, nr 43 (2018): 8160–68. http://dx.doi.org/10.1039/c8ob01825a.
Pełny tekst źródłaEldehna, Wagdy M., Ghada S. Hassan, Sara T. Al-Rashood, Hamad M. Alkahtani, Abdulrahman A. Almehizia i Ghada H. Al-Ansary. "Marine-Inspired Bis-indoles Possessing Antiproliferative Activity against Breast Cancer; Design, Synthesis, and Biological Evaluation". Marine Drugs 18, nr 4 (2.04.2020): 190. http://dx.doi.org/10.3390/md18040190.
Pełny tekst źródłaUruvakili, Anasuyamma, i 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, nr 12 (2019): 3275–84. http://dx.doi.org/10.1039/c9ob00232d.
Pełny tekst źródłaMacha, Lingamurthy, Deepak Singh, Hyong-Jin Rhee i Hyun-Joon Ha. "Lewis acid-mediated synthesis of mono- and tris-indole adducts from chiral aziridines". Organic & Biomolecular Chemistry 18, nr 46 (2020): 9473–82. http://dx.doi.org/10.1039/d0ob01865a.
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