Literatura académica sobre el tema "Indole N-alkylation"
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Artículos de revistas sobre el tema "Indole N-alkylation"
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 completoTesis sobre el tema "Indole N-alkylation"
Balestri, Lorenzo Jacopo Ilic. "SYNTHESIS OF ANTIFUNGAL COMPOUNDS". Doctoral thesis, Università di Siena, 2022. http://hdl.handle.net/11365/1203145.
Texto completoCharvieux, Aubin. "Autotransfert d’hydrogène catalysé par du nickel hétérogène pour la formation de liaisons C-C et C-N". Thesis, Lyon, 2019. http://www.theses.fr/2019LYSE1139.
Texto completoA wide range of nucleophiles could be alkylated through borrowing hydrogen methodology using alcohols as low toxicity alkylating agents. Advantageously, the only byproduct of these high atom economy reactions is water. In this context, nickel supported on silica-alumina (65 wt% Ni/SiO2-Al2O3) was used to create C-C bonds, particularly to perform the α-alkylation of ketones with alcohols, of which methanol. The full characterization of this catalyst was made, before and after use. Ni/SiO2-Al2O3 was found to be recyclable over 5 runs for the α-alkylation of acetophenone with benzyl alcohol. The cross-benzylation-methylation of acetophenone with methanol and benzyl alcohols was also studied. The α-benzylation of phenylacetonitrile by benzyl alcohol was performed with Ni/SiO2-Al2O3. This catalyst was also able to catalyse the N-alkylation of amides with alcohols. In this case, an important leaching of the catalyst in solution was observed. Finally, Ni/SiO2-Al2O3 was also efficient to catalyze an acceptorless dehydrogenative coupling, allowing the synthesis of an indole from aniline and a vicinal diol
Capítulos de libros sobre el tema "Indole N-alkylation"
Taber, Douglass F. "The Bradshaw/Bonjoch Synthesis of (-)-Anominine". En Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0097.
Texto completoTaber, Douglass. "Protection of Organic Functional Groups". En Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0011.
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