Artículos de revistas sobre el tema "Indole N-alkylation"
Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros
Consulte los 50 mejores artículos de revistas para su investigación sobre el tema "Indole N-alkylation".
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.
Yi, Zi-Juan, Jian-Ting Sun, Tian-Yu Yang, Xian-Yong Yu, Xiao-Li Han y Bang-Guo Wei. "Cu(OTf)2-catalyzed C3 aza-Friedel–Crafts alkylation of indoles with N,O-acetals". Organic & Biomolecular Chemistry 20, n.º 11 (2022): 2261–70. http://dx.doi.org/10.1039/d1ob02383g.
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 completoGardette, Daniel, Jean-Claude Gramain, Marie-Eve Lepage y Yves Troin. "Photocyclization of aryl enaminones. An efficient route to indole alkaloid synthons". Canadian Journal of Chemistry 67, n.º 2 (1 de febrero de 1989): 213–19. http://dx.doi.org/10.1139/v89-036.
Texto completoQiu, Zhongxuan, Rui Sun, Kun Yang y Dawei Teng. "Spiro Indane-Based Phosphine-Oxazolines as Highly Efficient P,N Ligands for Enantioselective Pd-Catalyzed Allylic Alkylation of Indoles and Allylic Etherification". Molecules 24, n.º 8 (21 de abril de 2019): 1575. http://dx.doi.org/10.3390/molecules24081575.
Texto completoWang, Chengyuan, Zhuopeng Li, Jiong Zhang y Xin-Ping Hui. "Asymmetric N-alkylation of indoles with isatins catalyzed by N-heterocyclic carbene: efficient synthesis of functionalized cyclic N,O-aminal indole derivatives". Organic Chemistry Frontiers 7, n.º 13 (2020): 1647–52. http://dx.doi.org/10.1039/d0qo00237b.
Texto completoKumar, Nivesh, Arindam Maity, Vipin R. Gavit y Alakesh Bisai. "A catalytic N-deacylative alkylation approach to hexahydropyrrolo[2,3-b]indole alkaloids". Chemical Communications 54, n.º 65 (2018): 9083–86. http://dx.doi.org/10.1039/c8cc04117b.
Texto completoDing, Zhenhua y Naohiko Yoshikai. "C2-Alkylation of N-pyrimidylindole with vinylsilane via cobalt-catalyzed C–H bond activation". Beilstein Journal of Organic Chemistry 8 (14 de septiembre de 2012): 1536–42. http://dx.doi.org/10.3762/bjoc.8.174.
Texto completoTrubitsõn, Dmitri, Jevgenija Martõnova, Kristin Erkman, Andrus Metsala, Jaan Saame, Kristjan Kõster, Ivar Järving, Ivo Leito y Tõnis Kanger. "Enantioselective N-Alkylation of Nitroindoles under Phase-Transfer Catalysis". Synthesis 52, n.º 07 (26 de noviembre de 2019): 1047–59. http://dx.doi.org/10.1055/s-0039-1690751.
Texto completoHuang, Bing-Bing, Liang Wu, Ren-Rong Liu, Ling-Ling Xing, Ren-Xiao Liang y Yi-Xia Jia. "Enantioselective Friedel–Crafts C2-alkylation of 3-substituted indoles with trifluoropyruvates and cyclic N-sulfonyl α-ketiminoesters". Organic Chemistry Frontiers 5, n.º 6 (2018): 929–32. http://dx.doi.org/10.1039/c7qo01014a.
Texto completoMérour, J. Y. y F. Cossais. "Regioselective N-Alkylation of Methyl Indole-2-carboxylate". Synthetic Communications 23, n.º 13 (julio de 1993): 1813–20. http://dx.doi.org/10.1080/00397919308011281.
Texto completoBhagwat, Shripad S. y Candido Gude. "N-alkylation of indole ring using Mitsunobu reaction". Tetrahedron Letters 35, n.º 12 (marzo de 1994): 1847–50. http://dx.doi.org/10.1016/s0040-4039(00)73177-7.
Texto completoShaikh, Iqbal N., Abdul Rahim, Shaikh Faazil, Syed Farooq Adil, Mohamed E. Assal y Mohammad Rafe Hatshan. "BF3-OEt2 Catalyzed C3-Alkylation of Indole: Synthesis of Indolylsuccinimidesand Their Cytotoxicity Studies". Molecules 26, n.º 8 (11 de abril de 2021): 2202. http://dx.doi.org/10.3390/molecules26082202.
Texto completoCai, Yue, Qing Gu y Shu-Li You. "Chemoselective N–H functionalization of indole derivatives via the Reissert-type reaction catalyzed by a chiral phosphoric acid". Organic & Biomolecular Chemistry 16, n.º 33 (2018): 6146–54. http://dx.doi.org/10.1039/c8ob01863d.
Texto completoGharpure, Santosh J. y Santosh K. Nanda. "Stereoselective synthesis of thiazino[4,3-a]indoles using the thia-Pictet–Spengler reaction of indoles bearing N-tethered thiols and vinylogous thiocarbonates". Organic & Biomolecular Chemistry 14, n.º 24 (2016): 5586–90. http://dx.doi.org/10.1039/c6ob00501b.
Texto completoSingh, Anil K. y Abera Asefa. "N‐Alkylation of Indole Compounds in Modified Wittig–Horner Reaction". Synthetic Communications 37, n.º 9 (mayo de 2007): 1491–94. http://dx.doi.org/10.1080/00397910701229073.
Texto completoMEROUR, J. Y. y F. COSSAIS. "ChemInform Abstract: Regioselective N-Alkylation of Methyl Indole-2-carboxylate." ChemInform 24, n.º 46 (20 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199346113.
Texto completoAlexy, Eric J., Tyler J. Fulton, Haiming Zhang y Brian M. Stoltz. "Palladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates". Chemical Science 10, n.º 23 (2019): 5996–6000. http://dx.doi.org/10.1039/c9sc01726g.
Texto completoKról, Marek, Grzegorz Ślifirski, Jerzy Kleps, Piotr Podsadni, Ilona Materek, Anna E. Kozioł y Franciszek Herold. "The Synthesis and Absolute Configuration of Enantiomeric Pure (R)- and (S)-3-(piperidin-3-yl)-1H-Indole Derivatives". International Journal of Molecular Sciences 24, n.º 1 (28 de diciembre de 2022): 517. http://dx.doi.org/10.3390/ijms24010517.
Texto completoKarchava, A. V., I. S. Shuleva, A. A. Ovcharenko y M. A. Yurovskaya. "2- and 3-phenylsulfonylindoles – synthetic equivalents of unsubstituted indole in N-alkylation reactions". Chemistry of Heterocyclic Compounds 46, n.º 3 (julio de 2010): 291–301. http://dx.doi.org/10.1007/s10593-010-0504-3.
Texto completoCohen, Peter A. y Louis A. Cohen. "Correlation of the effects of alkyl substituents on the basicities of indoles". Canadian Journal of Chemistry 70, n.º 1 (1 de enero de 1992): 282–84. http://dx.doi.org/10.1139/v92-039.
Texto completoLiu, Yanling, Xin Zhou, Deju Shang, Xiaohua Liu y Xiaoming Feng. "N,N′-Dioxide–scandium(III) complex catalyzed highly enantioselective Friedel–Crafts alkylation of indole to alkylidene malonates". Tetrahedron 66, n.º 7 (febrero de 2010): 1447–57. http://dx.doi.org/10.1016/j.tet.2009.12.032.
Texto completoItoh, Toshiyuki, Hiroyuki Uehara, Koji Ogiso, Shun Nomura, Shuichi Hayase y Motoi Kawatsura. "Alkylation of N-Protecting Group-free Indole with Vinyl Ketones Using Iron Salt Catalyst". Chemistry Letters 36, n.º 1 (enero de 2007): 50–51. http://dx.doi.org/10.1246/cl.2007.50.
Texto completoTrost, Barry M., Elumalai Gnanamani y Chao-I. Joey Hung. "Controlling Regioselectivity in the Enantioselective N-Alkylation of Indole Analogues Catalyzed by Dinuclear Zinc-ProPhenol". Angewandte Chemie International Edition 56, n.º 35 (19 de julio de 2017): 10451–56. http://dx.doi.org/10.1002/anie.201705315.
Texto completoTrost, Barry M., Elumalai Gnanamani y Chao-I. Joey Hung. "Controlling Regioselectivity in the Enantioselective N-Alkylation of Indole Analogues Catalyzed by Dinuclear Zinc-ProPhenol". Angewandte Chemie 129, n.º 35 (19 de julio de 2017): 10587–92. http://dx.doi.org/10.1002/ange.201705315.
Texto completoLiu, Yanling, Xin Zhou, Deju Shang, Xiaohua Liu y Xiaoming Feng. "ChemInform Abstract: N,N′-Dioxide-Scandium(III) Complex Catalyzed Highly Enantioselective Friedel-Crafts Alkylation of Indole to Alkylidene Malonates." ChemInform 41, n.º 24 (15 de junio de 2010): no. http://dx.doi.org/10.1002/chin.201024107.
Texto completoRossi, Sergio, Alessandra Puglisi, Laura Maria Raimondi y Maurizio Benaglia. "Stereolithography 3D-Printed Catalytically Active Devices in Organic Synthesis". Catalysts 10, n.º 1 (12 de enero de 2020): 109. http://dx.doi.org/10.3390/catal10010109.
Texto completoJorapur, Yogesh R., Jae Min Jeong y Dae Yoon Chi. "Potassium carbonate as a base for the N-alkylation of indole and pyrrole in ionic liquids". Tetrahedron Letters 47, n.º 14 (abril de 2006): 2435–38. http://dx.doi.org/10.1016/j.tetlet.2006.01.129.
Texto completoMino, Takashi, Shingo Komatsu, Kazuya Wakui, Haruka Yamada, Hiroaki Saotome, Masami Sakamoto y Tsutomu Fujita. "N-Aryl indole-derived C–N bond axially chiral phosphine ligands: synthesis and application in palladium-catalyzed asymmetric allylic alkylation". Tetrahedron: Asymmetry 21, n.º 6 (abril de 2010): 711–18. http://dx.doi.org/10.1016/j.tetasy.2010.03.039.
Texto completoGallo, Roger y Mohamed Bourak. "Improving Regioselectivity under Phase Transfer Conditions: Effect of Chemical Parameters and Kinetic Study of Indole N-Alkylation". HETEROCYCLES 31, n.º 3 (1990): 447. http://dx.doi.org/10.3987/com-88-4855.
Texto completoHong, Liang, Wangsheng Sun, Chunxia Liu, Lei Wang y Rui Wang. "Asymmetric Organocatalytic N-Alkylation of Indole-2-carbaldehydes with α,β-Unsaturated Aldehydes: One-Pot Synthesis of Chiral Pyrrolo[1,2-a]indole-2-carbaldehydes". Chemistry - A European Journal 16, n.º 2 (11 de enero de 2010): 440–44. http://dx.doi.org/10.1002/chem.200902638.
Texto completoHong, Liang, Wangsheng Sun, Chunxia Liu, Lei Wang y Rui Wang. "Asymmetric Organocatalytic N-Alkylation of Indole-2-carbaldehydes with α,β-Unsaturated Aldehydes: One-Pot Synthesis of Chiral Pyrrolo[1,2-a]indole-2-carbaldehydes". Chemistry - A European Journal 16, n.º 3 (14 de enero de 2010): 746. http://dx.doi.org/10.1002/chem.201090006.
Texto completoKuvshinova, Sofya S., Yulia V. Nelyubina, Vladimir A. Larionov, Daria V. Vorobyeva, Sergey N. Osipov y Dmitry A. Loginov. "Half-sandwich complexes of group 9 metals with N,Nʹ-ligands for CF3-carbenoid alkylation of N-(pyrimidin-2-yl)indole". Journal of Organometallic Chemistry 946-947 (agosto de 2021): 121899. http://dx.doi.org/10.1016/j.jorganchem.2021.121899.
Texto completoLi, Nai-Kai, Jun-Qi Zhang, Bing-Bing Sun, Hai-Yan Li y Xing-Wang Wang. "Chiral Diphosphine–Palladium-Catalyzed Sequential Asymmetric Double-Friedel–Crafts Alkylation and N-Hemiketalization for Spiro-polycyclic Indole Derivatives". Organic Letters 19, n.º 8 (13 de abril de 2017): 1954–57. http://dx.doi.org/10.1021/acs.orglett.7b00368.
Texto completoShi, Yan-Chao, Shou-Guo Wang, Qin Yin y Shu-Li You. "N-alkylation of indole via ring-closing metathesis/isomerization/Mannich cascade under ruthenium/chiral phosphoric acid sequential catalysis". Org. Chem. Front. 1, n.º 1 (2014): 39–43. http://dx.doi.org/10.1039/c3qo00008g.
Texto completoLodeiro, Carlos, Rufina Bastida, Emilia Bértolo y Adolfo Rodríguez. "A new family of NxOy pyridine-containing macrocycles: Synthesis and characterization of their Y(III), Ln(III), Zn(II), and Cd(II) coordination compounds". Canadian Journal of Chemistry 82, n.º 3 (1 de marzo de 2004): 437–47. http://dx.doi.org/10.1139/v03-214.
Texto completoHarkov, Stefan. "SYNTHESIS AND CONVERSION OF NEW POTENTIALLY BIOLOGICALLY ACTIVE 4-THIAZOLIDINONE DERIVATIVES WITH A TRIAZINOINDOLE FRAGMENT IN THE MOLECULES". KNOWLEDGE - International Journal 54, n.º 4 (30 de septiembre de 2022): 677–81. http://dx.doi.org/10.35120/kij5404677h.
Texto completoWang, Shuai, Yao-Bin Shen, Long-Fei Li, Bin Qiu, Liping Yu, Qing Liu y Jian Xiao. "N-Alkylation-Initiated Redox-Neutral [5 + 2] Annulation of 3-Alkylindoles with o-Aminobenzaldehydes: Access to Indole-1,2-Fused 1,4-Benzodiazepines". Organic Letters 21, n.º 22 (7 de noviembre de 2019): 8904–8. http://dx.doi.org/10.1021/acs.orglett.9b03011.
Texto completoBHAGWAT, S. S. y C. GUDE. "ChemInform Abstract: Thromboxane Receptor Antagonism Combined with Thromboxane Synthase Inhibition. Part 8. N-Alkylation of the Indole Ring Using the Mitsunobu Reaction." ChemInform 25, n.º 30 (19 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199430115.
Texto completoBora, Darshana, Stephy Elza John, Mary Sravani Galla, Manda Sathish y Nagula Shankaraiah. "Rh(III)-catalysed site-selective alkylation of β-carbolines/isoquinolines and tandem C H/C N functionalization to construct indolizine-indole frameworks". Molecular Catalysis 533 (diciembre de 2022): 112783. http://dx.doi.org/10.1016/j.mcat.2022.112783.
Texto completoMayer, Szabolcs, András Keglevich, Csilla Sepsey Für, Hedvig Bölcskei, Viktor Ilkei, Péter Keglevich y László Hazai. "Results in Chemistry of Natural Organic Compounds. Synthesis of New Anticancer Vinca Alkaloids and Flavone Alkaloids". Chemistry 2, n.º 3 (10 de agosto de 2020): 714–26. http://dx.doi.org/10.3390/chemistry2030046.
Texto completoMottinelli, Marco, Mathew P. Leese y Barry V. L. Potter. "Accessing simply-substituted 4-hydroxytetrahydroisoquinolines via Pomeranz–Fritsch–Bobbitt reaction with non-activated and moderately-activated systems". Beilstein Journal of Organic Chemistry 13 (6 de septiembre de 2017): 1871–78. http://dx.doi.org/10.3762/bjoc.13.182.
Texto completoCrich, David y Xianhai Huang. "ChemInform Abstract: Reaction of Tryptophan Derivatives with N-Phenylselenyl Phthalimide: The Nature of the Kinetic and Thermodynamic Hexahydropyrrolo[2,3-b]indole Products. Alkylation of Tryptophan with Inversion of Configuration." ChemInform 31, n.º 2 (11 de junio de 2010): no. http://dx.doi.org/10.1002/chin.200002192.
Texto completoLing, Li, Jing Cao, Jianfeng Hu y Hao Zhang. "Copper-catalyzed N-alkylation of indoles by N-tosylhydrazones". RSC Advances 7, n.º 45 (2017): 27974–80. http://dx.doi.org/10.1039/c7ra03765a.
Texto completoGao, Yadong, Jianhua Li, Songlin Bai, Daoquan Tu, Chao Yang, Zhiwen Ye, Bingcheng Hu, Xiangbing Qi y Chao Jiang. "Direct synthesis of annulated indoles through palladium-catalyzed double alkylations". Organic Chemistry Frontiers 7, n.º 9 (2020): 1149–57. http://dx.doi.org/10.1039/d0qo00135j.
Texto completoChen, Jian-Ping, Wen-Wen Chen, Yi Li y Ming-Hua Xu. "A highly diastereoselective Friedel–Crafts reaction of indoles with isatin-derived N-sulfinyl ketimines towards the efficient synthesis of chiral tetrasubstituted 3-indolyl-3-aminooxindoles". Organic & Biomolecular Chemistry 13, n.º 11 (2015): 3363–70. http://dx.doi.org/10.1039/c5ob00063g.
Texto completoSiddiki, S. M. A. Hakim, Kenichi Kon y Ken-ichi Shimizu. "Selective N-alkylation of indoles with primary alcohols using a Pt/HBEA catalyst". Green Chemistry 17, n.º 1 (2015): 173–77. http://dx.doi.org/10.1039/c4gc01419g.
Texto completoMino, Takashi, Kenji Nishikawa, Moeko Asano, Yamato Shima, Toshibumi Ebisawa, Yasushi Yoshida y Masami Sakamoto. "Chiral N-1-adamantyl-N-trans-cinnamylaniline type ligands: synthesis and application to palladium-catalyzed asymmetric allylic alkylation of indoles". Organic & Biomolecular Chemistry 14, n.º 31 (2016): 7509–19. http://dx.doi.org/10.1039/c6ob01354f.
Texto completoFink, David M. "Cesium Carbonate Promoted N-Alkylation of Indoles". Synlett, n.º 13 (2004): 2394–96. http://dx.doi.org/10.1055/s-2004-832836.
Texto completoZhang, Lvye, Binqiang Wu, Zhangtao Chen, Jinjin Hu, Xiaofei Zeng y Guofu Zhong. "Chiral phosphoric acid catalyzed enantioselective N-alkylation of indoles with in situ generated cyclic N-acyl ketimines". Chemical Communications 54, n.º 66 (2018): 9230–33. http://dx.doi.org/10.1039/c8cc05073b.
Texto completoHu, Miao, Yong Jiang, Nan Sun, Baoxiang Hu, Zhenlu Shen, Xinquan Hu y Liqun Jin. "Nickel-catalyzed C3-alkylation of indoles with alcohols via a borrowing hydrogen strategy". New Journal of Chemistry 45, n.º 22 (2021): 10057–62. http://dx.doi.org/10.1039/d1nj01581h.
Texto completo