Добірка наукової літератури з теми "Indole N-alkylation"
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Статті в журналах з теми "Indole N-alkylation"
Yi, Zi-Juan, Jian-Ting Sun, Tian-Yu Yang, Xian-Yong Yu, Xiao-Li Han, and Bang-Guo Wei. "Cu(OTf)2-catalyzed C3 aza-Friedel–Crafts alkylation of indoles with N,O-acetals." Organic & Biomolecular Chemistry 20, no. 11 (2022): 2261–70. http://dx.doi.org/10.1039/d1ob02383g.
Повний текст джерелаTrubitsõn, Dmitri, and Tõnis Kanger. "Enantioselective Catalytic Synthesis of N-alkylated Indoles." Symmetry 12, no. 7 (July 17, 2020): 1184. http://dx.doi.org/10.3390/sym12071184.
Повний текст джерелаGardette, Daniel, Jean-Claude Gramain, Marie-Eve Lepage, and Yves Troin. "Photocyclization of aryl enaminones. An efficient route to indole alkaloid synthons." Canadian Journal of Chemistry 67, no. 2 (February 1, 1989): 213–19. http://dx.doi.org/10.1139/v89-036.
Повний текст джерелаQiu, Zhongxuan, Rui Sun, Kun Yang, and 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, no. 8 (April 21, 2019): 1575. http://dx.doi.org/10.3390/molecules24081575.
Повний текст джерелаWang, Chengyuan, Zhuopeng Li, Jiong Zhang, and 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, no. 13 (2020): 1647–52. http://dx.doi.org/10.1039/d0qo00237b.
Повний текст джерелаKumar, Nivesh, Arindam Maity, Vipin R. Gavit, and Alakesh Bisai. "A catalytic N-deacylative alkylation approach to hexahydropyrrolo[2,3-b]indole alkaloids." Chemical Communications 54, no. 65 (2018): 9083–86. http://dx.doi.org/10.1039/c8cc04117b.
Повний текст джерелаDing, Zhenhua, and Naohiko Yoshikai. "C2-Alkylation of N-pyrimidylindole with vinylsilane via cobalt-catalyzed C–H bond activation." Beilstein Journal of Organic Chemistry 8 (September 14, 2012): 1536–42. http://dx.doi.org/10.3762/bjoc.8.174.
Повний текст джерелаTrubitsõn, Dmitri, Jevgenija Martõnova, Kristin Erkman, Andrus Metsala, Jaan Saame, Kristjan Kõster, Ivar Järving, Ivo Leito, and Tõnis Kanger. "Enantioselective N-Alkylation of Nitroindoles under Phase-Transfer Catalysis." Synthesis 52, no. 07 (November 26, 2019): 1047–59. http://dx.doi.org/10.1055/s-0039-1690751.
Повний текст джерелаHuang, Bing-Bing, Liang Wu, Ren-Rong Liu, Ling-Ling Xing, Ren-Xiao Liang та Yi-Xia Jia. "Enantioselective Friedel–Crafts C2-alkylation of 3-substituted indoles with trifluoropyruvates and cyclic N-sulfonyl α-ketiminoesters". Organic Chemistry Frontiers 5, № 6 (2018): 929–32. http://dx.doi.org/10.1039/c7qo01014a.
Повний текст джерелаMérour, J. Y., and F. Cossais. "Regioselective N-Alkylation of Methyl Indole-2-carboxylate." Synthetic Communications 23, no. 13 (July 1993): 1813–20. http://dx.doi.org/10.1080/00397919308011281.
Повний текст джерелаДисертації з теми "Indole N-alkylation"
Balestri, Lorenzo Jacopo Ilic. "SYNTHESIS OF ANTIFUNGAL COMPOUNDS." Doctoral thesis, Università di Siena, 2022. http://hdl.handle.net/11365/1203145.
Повний текст джерелаCharvieux, 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.
Повний текст джерелаA 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
Частини книг з теми "Indole N-alkylation"
Taber, Douglass F. "The Bradshaw/Bonjoch Synthesis of (-)-Anominine." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0097.
Повний текст джерелаTaber, Douglass. "Protection of Organic Functional Groups." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0011.
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