Artículos de revistas sobre el tema "Cycloaddition of pyrroles"
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Hu, Fan, Jerome Ng y Pauline Chiu. "Pyrroles as Dienes in (4+3) Cycloadditions". Synthesis 51, n.º 05 (6 de febrero de 2019): 1073–86. http://dx.doi.org/10.1055/s-0037-1611660.
Texto completoGao, Meng, Wenting Zhao, Hongyi Zhao, Ziyun Lin, Dongfeng Zhang y Haihong Huang. "An efficient and facile access to highly functionalized pyrrole derivatives". Beilstein Journal of Organic Chemistry 14 (20 de abril de 2018): 884–90. http://dx.doi.org/10.3762/bjoc.14.75.
Texto completoLi, Jin-Heng, De-Lie An y Jing-Hao Qin. "Recent Advances in Cycloaddition Reactions with Alkynes to Construct Heterocycles". Synthesis 52, n.º 24 (13 de octubre de 2020): 3818–36. http://dx.doi.org/10.1055/s-0040-1707355.
Texto completoSleziak, Róbert y Alžbeta Krutošíková. "Cycloaddition Reactions of Furo[2,3-b]pyrroles". Collection of Czechoslovak Chemical Communications 64, n.º 2 (1999): 321–28. http://dx.doi.org/10.1135/cccc19990321.
Texto completoMotornov, Vladimir A., Andrey A. Tabolin, Yulia V. Nelyubina, Valentine G. Nenajdenko y Sema L. Ioffe. "Copper-catalyzed [3 + 2]-cycloaddition of α-halonitroalkenes with azomethine ylides: facile synthesis of multisubstituted pyrrolidines and pyrroles". Organic & Biomolecular Chemistry 19, n.º 15 (2021): 3413–27. http://dx.doi.org/10.1039/d1ob00146a.
Texto completoKrutošíková, Alžbeta. "Synthesis and reactions of condensed furan derivatives". Collection of Czechoslovak Chemical Communications 55, n.º 3 (1990): 597–621. http://dx.doi.org/10.1135/cccc19900597.
Texto completoGuo, Tenglong, Quanbin Jiang y Zhengkun Yu. "Palladium-catalyzed oxidative annulation of in situ generated enones to pyrroles: a concise route to functionalized indoles". Organic Chemistry Frontiers 2, n.º 10 (2015): 1361–65. http://dx.doi.org/10.1039/c5qo00203f.
Texto completoKrutošíková, Alžbeta, Miloslava Dandárová, Juraj Alföldi y Jaroslav Kováč. "Addition and cycloaddition reactions of furo[3,2-b]pyrroles and their benzo[b] analogues: An NMR study of structure of products". Collection of Czechoslovak Chemical Communications 53, n.º 8 (1988): 1770–78. http://dx.doi.org/10.1135/cccc19881770.
Texto completoLakhlifi, Tahar, Ahmed Sedqui, Toufik Fathi, Bernard Laude y Jean-François Robert. "Double diastéréosélectivité de la cycloaddition dipolaire-1,3 d'ylures d'azométhine cycliques substitués". Canadian Journal of Chemistry 72, n.º 6 (1 de junio de 1994): 1417–23. http://dx.doi.org/10.1139/v94-178.
Texto completoZhou, Kai, Ming Bao, Jingjing Huang, Zhenghui Kang, Xinfang Xu, Wenhao Hu y Yu Qian. "Iron-catalyzed [3 + 2]-cycloaddition of in situ generated N-ylides with alkynes or olefins: access to multi-substituted/polycyclic pyrrole derivatives". Organic & Biomolecular Chemistry 18, n.º 3 (2020): 409–14. http://dx.doi.org/10.1039/c9ob02571e.
Texto completoLin, Zhang-qi, Chao-dong Li, Zi-chun Zhou, Shuai Xue, Jian-rong Gao, Qing Ye y Yu-jin Li. "Copper(II)-Promoted Oxidation/[3+2]Cycloaddition/Aromatization Cascade: Efficient Synthesis of Tetrasubstituted NH-Pyrrole from Chalcones and Iminodiacetates". Synlett 30, n.º 12 (12 de junio de 2019): 1442–46. http://dx.doi.org/10.1055/s-0039-1689972.
Texto completoLi, Chengjie, Martin Fechtel, Yaqing Feng y Bernhard Kräutler. "Corroles programmed for regioselective cycloaddition chemistry — synthesis of a bisadduct with C60-fullerene". Journal of Porphyrins and Phthalocyanines 16, n.º 05n06 (mayo de 2012): 556–63. http://dx.doi.org/10.1142/s108842461250054x.
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 completoXie, Ying, Tengfei Chen, Shaomin Fu, Xing-Shu Li, Yuanfu Deng, Huanfeng Jiang y Wei Zeng. "Pd-Catalyzed [3+2] cycloaddition of ketoimines with alkynes via directed sp3 C–H bond activation". Chem. Commun. 50, n.º 73 (2014): 10699–702. http://dx.doi.org/10.1039/c4cc04676e.
Texto completoWang, Hai-Ying, Ming Bao, Bo Jiang y Liang Li. "Base-mediated isocyanide-based three-component reactions: divergent synthesis of spiro-substituted furans and pyrroles". RSC Advances 6, n.º 8 (2016): 6459–66. http://dx.doi.org/10.1039/c5ra25408f.
Texto completoSalehi, Parvin, Zahra Tanbakouchian, Noushin Farajinia-Lehi y Morteza Shiri. "Cascade synthesis of 2,4-disulfonylpyrroles by the sulfonylation/[2 + 3]-cycloaddition reactions of gem-dibromoalkenes with arylsulfonyl methyl isocyanides". RSC Advances 11, n.º 22 (2021): 13292–96. http://dx.doi.org/10.1039/d0ra10451e.
Texto completoZhou, Ming-Bo, Rui Pi, Fan Teng, Yang Li y Jin-Heng Li. "Ring-opening formal hetero-[5+2] cycloaddition of 1-tosyl-2,3-dihydro-1H-pyrroles with terminal alkynes: entry to 1-tosyl-2,3-dihydro 2,3-dihydro-1H-azepines". Chemical Communications 55, n.º 75 (2019): 11295–98. http://dx.doi.org/10.1039/c9cc05082e.
Texto completoIto, S., Y. Tokimaru y K. Nozaki. "Isoquinolino[4,3,2-de]phenanthridine: synthesis and its use in 1,3-dipolar cycloadditions to form nitrogen-containing polyaromatic hydrocarbons". Chemical Communications 51, n.º 1 (2015): 221–24. http://dx.doi.org/10.1039/c4cc06643j.
Texto completoBoudriga, Sarra, Mohiedinne Askri, Mohamed Rammah y Karin Monnier-Jobé. "Reaction of 2-Benzoyl-1,2-Dihydroisoquinoline-1-Carbonitrile Tetrafluoroborate Salt with 2-Arylmethylene-1,3-Indanediones. Regio- and Stereochemistry of the Reaction. Formation of Spiro Compounds". Journal of Chemical Research 2003, n.º 4 (abril de 2003): 208–10. http://dx.doi.org/10.3184/030823403103173499.
Texto completoLi, Qing, Chuan-Jin Hou, Yun-Ze Hui, Yan-Jun Liu, Rui-Feng Yang y Xiang-Ping Hu. "Tridentate P,N,N-ligand promoted copper-catalyzed [3 + 2] cycloaddition of propargylic esters with β-enamino esters: synthesis of highly functionalized pyrroles". RSC Advances 5, n.º 104 (2015): 85879–83. http://dx.doi.org/10.1039/c5ra19304d.
Texto completoWang, Kai-Kai, Yan-Xin Xie, Yan-Li Li, Rongxiang Chen y Zhan-Yong Wang. "Dearomative [3 + 2] cycloaddition reaction of nitrobenzothiophenes with nonstabilized azomethine ylides". RSC Advances 10, n.º 48 (2020): 28720–24. http://dx.doi.org/10.1039/d0ra05687a.
Texto completoPrasad, Pulaganti Vijaya, Medi Shanker, Avudoddi Venkanna, Marapala Kumara Swamy, K. Gopichand y Pallapothula Venkateswar Rao. "Synthesis of functionalized pyrroles and fused pyrroles through intermolecular [3 + 2] cycloaddition reaction". Synthetic Communications 48, n.º 9 (27 de marzo de 2018): 1040–44. http://dx.doi.org/10.1080/00397911.2018.1433301.
Texto completoGerster, Holger y Gerhard Maas. "Diverse Reactivities of Acetylenic Iminium Salts Toward 1,3-Oxazolium-5-olates (Münchnones)". Zeitschrift für Naturforschung B 63, n.º 4 (1 de abril de 2008): 384–94. http://dx.doi.org/10.1515/znb-2008-0405.
Texto completoKoçak, Ramazan y Arif Daştan. "Synthesis of dibenzosuberenone-based novel polycyclic π-conjugated dihydropyridazines, pyridazines and pyrroles". Beilstein Journal of Organic Chemistry 17 (15 de marzo de 2021): 719–29. http://dx.doi.org/10.3762/bjoc.17.61.
Texto completoChen, Xiu-Yu, Hui Zheng, Ying Han, Jing Sun y Chao-Guo Yan. "The unique reactivity of 5,6-unsubstituted 1,4-dihydropyridine in the Huisgen 1,4-diploar cycloaddition and formal [2 + 2] cycloaddition". Beilstein Journal of Organic Chemistry 19 (29 de junio de 2023): 982–90. http://dx.doi.org/10.3762/bjoc.19.73.
Texto completoSleziak, Robert y Alzbeta Krutosikova. "ChemInform Abstract: Cycloaddition Reactions of Furo[2,3-b]pyrroles." ChemInform 30, n.º 31 (14 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199931048.
Texto completoRastogi, Namrata, Lalita Devi, Poornima Mishra y Ayushi Pokhriyal. "Organo-photocatalytic Synthesis of Functionalized Pyrroles from 2H-Azirines and α-Substituted Nitroalkenes". SynOpen 06, n.º 03 (23 de agosto de 2022): 198–207. http://dx.doi.org/10.1055/s-0042-1751360.
Texto completoKalmode, Hanuman P., Kamlesh S. Vadagaonkar, Kaliyappan Murugan y Atul C. Chaskar. "A multicomponent pathway-inspired regioselective synthesis of 2,3,4-trisubstituted 1H-pyrroles via [3+2] cycloaddition reaction". New Journal of Chemistry 39, n.º 6 (2015): 4631–39. http://dx.doi.org/10.1039/c5nj00302d.
Texto completoShibata, Miki, Ryuichi Fuchigami, Ryota Kotaka, Kosuke Namba y Keiji Tanino. "Acid-catalyzed [4+3] cycloaddition reaction of N-nosyl pyrroles". Tetrahedron 71, n.º 26-27 (julio de 2015): 4495–99. http://dx.doi.org/10.1016/j.tet.2015.02.071.
Texto completoMoiseev, S. V. y N. V. Vasil'ev. "Synthesis and cycloaddition of N-substituted pyrroles with polyfluorinated substituents". Russian Chemical Bulletin 54, n.º 8 (agosto de 2005): 1948–53. http://dx.doi.org/10.1007/s11172-006-0063-z.
Texto completoMarkitanov, Yuriy N., Vadim M. Timoshenko, Eduard B. Rusanov y Yuriy G. Shermolovich. "[3+2] Cycloaddition reactions of 1-substituted 3,3,3-trifluoropropenes with isonitriles – synthesis of pyrroles and pyrrolines". Chemistry of Heterocyclic Compounds 57, n.º 3 (marzo de 2021): 253–60. http://dx.doi.org/10.1007/s10593-021-02901-x.
Texto completoWang, Zhen-Hua, Tong Zhang, Li-Wen Shen, Xiu Yang, Yan-Ping Zhang, Yong You, Jian-Qiang Zhao y Wei-Cheng Yuan. "Diverse Synthesis of Fused Polyheterocyclic Compounds via [3 + 2] Cycloaddition of In Situ-Generated Heteroaromatic N-Ylides and Electron-Deficient Olefins". Molecules 28, n.º 11 (29 de mayo de 2023): 4410. http://dx.doi.org/10.3390/molecules28114410.
Texto completoJones, Raymond C. F., Kevin J. Howard, John R. Nichols y John S. Snaith. "Annulation of dihydroimidazoles: a 1,3-dipolar cycloaddition route to pyrrolo[1,2-a]imidazoles, pyrrolidines and pyrroles". Journal of the Chemical Society, Perkin Transactions 1, n.º 13 (1998): 2061–72. http://dx.doi.org/10.1039/a802048e.
Texto completoFuchigami, Ryuichi, Kosuke Namba y Keiji Tanino. "Concise [4+3] cycloaddition reaction of pyrroles leading to tropinone derivatives". Tetrahedron Letters 53, n.º 43 (octubre de 2012): 5725–28. http://dx.doi.org/10.1016/j.tetlet.2012.07.130.
Texto completoEddaif, A., S. Kitane, M. Soufiaoui y P. Mison. "Cycloaddition dipolaire −1,3 sur des 2H-pyrroles: synthèse de quelques dérivés de pyrazolino- et isoxazolino- [5,6-e] pyrroles". Tetrahedron Letters 32, n.º 30 (julio de 1991): 3709–10. http://dx.doi.org/10.1016/s0040-4039(00)79774-7.
Texto completoGaleev, Andrew R., Anna A. Moroz, Maksim V. Dmitriev y Andrey N. Maslivets. "Cycloaddition of Huisgen 1,4-dipoles: synthesis and rapid epimerization of functionalized spiropyrido[2,1-b][1,3]oxazine-pyrroles and related products". RSC Advances 12, n.º 1 (2022): 578–87. http://dx.doi.org/10.1039/d1ra08384h.
Texto completoKim, Ikyon, Hee-Kyung Na, Kyung Kim, Sun Kim y Ge Lee. "A Novel [3+2] Dipolar Cycloaddition Approach to Hexahydrobenzofuro[3,2-b]pyrroles". Synlett 2008, n.º 13 (15 de julio de 2008): 2069–71. http://dx.doi.org/10.1055/s-2008-1077951.
Texto completoKim, Yongju, Jonghoon Kim y Seung Bum Park. "Regioselective Synthesis of Tetrasubstituted Pyrroles by 1,3-Dipolar Cycloaddition and Spontaneous Decarboxylation". Organic Letters 11, n.º 1 (enero de 2009): 17–20. http://dx.doi.org/10.1021/ol8022193.
Texto completoCox, Joshua B. y John L. Wood. "Synthetic studies toward longeracemine: The intramolecular [4+2] cycloaddition of 3H-pyrroles". Tetrahedron 74, n.º 35 (agosto de 2018): 4539–49. http://dx.doi.org/10.1016/j.tet.2018.07.024.
Texto completoShibata, Miki, Ryuichi Fuchigami, Ryota Kotaka, Kosuke Namba y Keiji Tanino. "ChemInform Abstract: Acid-Catalyzed [4 + 3] Cycloaddition Reaction of N-Nosyl Pyrroles." ChemInform 46, n.º 42 (octubre de 2015): no. http://dx.doi.org/10.1002/chin.201542132.
Texto completoIvan, Beatrice-Cristina, Stefania-Felicia Barbuceanu, Camelia Mia Hotnog, Adriana Iuliana Anghel, Robert Viorel Ancuceanu, Mirela Antonela Mihaila, Lorelei Irina Brasoveanu et al. "New Pyrrole Derivatives as Promising Biological Agents: Design, Synthesis, Characterization, In Silico, and Cytotoxicity Evaluation". International Journal of Molecular Sciences 23, n.º 16 (9 de agosto de 2022): 8854. http://dx.doi.org/10.3390/ijms23168854.
Texto completoEDDAIF, A., S. KITANE, M. SOUFIAOUI y P. MISON. "ChemInform Abstract: 1,3-Dipolar Cycloaddition Reaction with 2H-Pyrroles: Synthesis of Some Pyrazolino- and Isoxazolino(5,6-e)pyrrole Derivatives." ChemInform 23, n.º 18 (22 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199218076.
Texto completoJONES, R. C. F., K. J. HOWARD, J. R. NICHOLS y J. S. SNAITH. "ChemInform Abstract: Annulation of Dihydroimidazoles: A 1,3-Dipolar Cycloaddition Route to Pyrrolo[1,2-a]imidazoles, Pyrrolidines and Pyrroles." ChemInform 29, n.º 49 (18 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199849147.
Texto completoZhu, Guodong, Shiqi Wu, Xiaoze Bao, Longchen Cui, Yanpeng Zhang, Jingping Qu, Hongbo Chen y Baomin Wang. "Asymmetric [3+2] cycloaddition of 3-amino oxindole-based azomethine ylides with α,β-ynones: a straightforward approach to spirooxindoles incorporating 2,5-dihydropyrroles and pyrroles". Chemical Communications 53, n.º 34 (2017): 4714–17. http://dx.doi.org/10.1039/c7cc01653k.
Texto completoLin, Zhang-qi, Chao-dong Li, Jun-yi Su, Wen-jie Niu, Jian-rong Gao y Yu-jin Li. "Sequential Cu(II)-promoted oxidation/[3 + 2] cycloaddition/aromatization tandem reaction for the synthesis of 2-substituted benzo[f]isoindole-4,9-dione". Canadian Journal of Chemistry 98, n.º 11 (noviembre de 2020): 690–96. http://dx.doi.org/10.1139/cjc-2019-0108.
Texto completoEfremova, Mariia M., Alexander S. Novikov, Rafael R. Kostikov, Taras L. Panikorovsky, Andrey V. Ivanov y Alexander P. Molchanov. "Regio- and diastereoselectivity of the cycloaddition of nitrones with N-propadienylindole and pyrroles". Tetrahedron 74, n.º 1 (enero de 2018): 174–83. http://dx.doi.org/10.1016/j.tet.2017.11.056.
Texto completoJones, Raymond C. F., John R. Nichols y Michael T. Cox. "Annulation of imidazolines: A 1,3-dipolar cycloaddition route to pyrroloimidazoles, pyrrolidines and pyrroles". Tetrahedron Letters 31, n.º 16 (enero de 1990): 2333–36. http://dx.doi.org/10.1016/0040-4039(90)80221-7.
Texto completoWang, Zheng, Ying Shi, Xiaoyan Luo, De-Man Han y Wei-Ping Deng. "Direct synthesis of pyrroles via 1,3-dipolar cycloaddition of azomethine ylides with ynones". New Journal of Chemistry 37, n.º 6 (2013): 1742. http://dx.doi.org/10.1039/c3nj00067b.
Texto completoJursic, Branko S. "Cycloaddition extrusion reactions in the preparation of pyrroles. A DFT-AM1 theoretical study". Journal of Molecular Structure: THEOCHEM 365, n.º 1 (junio de 1996): 55–61. http://dx.doi.org/10.1016/0166-1280(95)04468-x.
Texto completoLiu, Jianquan, Zhongxue Fang, Qian Zhang, Qun Liu y Xihe Bi. "Silver-Catalyzed Isocyanide-Alkyne Cycloaddition: A General and Practical Method to Oligosubstituted Pyrroles". Angewandte Chemie 125, n.º 27 (6 de mayo de 2013): 7091–95. http://dx.doi.org/10.1002/ange.201302024.
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