Статті в журналах з теми "Indole N-alkylation"
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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 джерелаBhagwat, Shripad S., and Candido Gude. "N-alkylation of indole ring using Mitsunobu reaction." Tetrahedron Letters 35, no. 12 (March 1994): 1847–50. http://dx.doi.org/10.1016/s0040-4039(00)73177-7.
Повний текст джерелаShaikh, Iqbal N., Abdul Rahim, Shaikh Faazil, Syed Farooq Adil, Mohamed E. Assal, and Mohammad Rafe Hatshan. "BF3-OEt2 Catalyzed C3-Alkylation of Indole: Synthesis of Indolylsuccinimidesand Their Cytotoxicity Studies." Molecules 26, no. 8 (April 11, 2021): 2202. http://dx.doi.org/10.3390/molecules26082202.
Повний текст джерелаCai, Yue, Qing Gu, and 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, no. 33 (2018): 6146–54. http://dx.doi.org/10.1039/c8ob01863d.
Повний текст джерелаGharpure, Santosh J., and 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, no. 24 (2016): 5586–90. http://dx.doi.org/10.1039/c6ob00501b.
Повний текст джерелаSingh, Anil K., and Abera Asefa. "N‐Alkylation of Indole Compounds in Modified Wittig–Horner Reaction." Synthetic Communications 37, no. 9 (May 2007): 1491–94. http://dx.doi.org/10.1080/00397910701229073.
Повний текст джерелаMEROUR, J. Y., and F. COSSAIS. "ChemInform Abstract: Regioselective N-Alkylation of Methyl Indole-2-carboxylate." ChemInform 24, no. 46 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199346113.
Повний текст джерелаAlexy, Eric J., Tyler J. Fulton, Haiming Zhang, and Brian M. Stoltz. "Palladium-catalyzed enantioselective decarboxylative allylic alkylation of fully substituted N-acyl indole-derived enol carbonates." Chemical Science 10, no. 23 (2019): 5996–6000. http://dx.doi.org/10.1039/c9sc01726g.
Повний текст джерелаKról, Marek, Grzegorz Ślifirski, Jerzy Kleps, Piotr Podsadni, Ilona Materek, Anna E. Kozioł, and 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, no. 1 (December 28, 2022): 517. http://dx.doi.org/10.3390/ijms24010517.
Повний текст джерелаKarchava, A. V., I. S. Shuleva, A. A. Ovcharenko, and M. A. Yurovskaya. "2- and 3-phenylsulfonylindoles – synthetic equivalents of unsubstituted indole in N-alkylation reactions." Chemistry of Heterocyclic Compounds 46, no. 3 (July 2010): 291–301. http://dx.doi.org/10.1007/s10593-010-0504-3.
Повний текст джерелаCohen, Peter A., and Louis A. Cohen. "Correlation of the effects of alkyl substituents on the basicities of indoles." Canadian Journal of Chemistry 70, no. 1 (January 1, 1992): 282–84. http://dx.doi.org/10.1139/v92-039.
Повний текст джерелаLiu, Yanling, Xin Zhou, Deju Shang, Xiaohua Liu, and Xiaoming Feng. "N,N′-Dioxide–scandium(III) complex catalyzed highly enantioselective Friedel–Crafts alkylation of indole to alkylidene malonates." Tetrahedron 66, no. 7 (February 2010): 1447–57. http://dx.doi.org/10.1016/j.tet.2009.12.032.
Повний текст джерелаItoh, Toshiyuki, Hiroyuki Uehara, Koji Ogiso, Shun Nomura, Shuichi Hayase, and Motoi Kawatsura. "Alkylation of N-Protecting Group-free Indole with Vinyl Ketones Using Iron Salt Catalyst." Chemistry Letters 36, no. 1 (January 2007): 50–51. http://dx.doi.org/10.1246/cl.2007.50.
Повний текст джерелаTrost, Barry M., Elumalai Gnanamani, and Chao-I. Joey Hung. "Controlling Regioselectivity in the Enantioselective N-Alkylation of Indole Analogues Catalyzed by Dinuclear Zinc-ProPhenol." Angewandte Chemie International Edition 56, no. 35 (July 19, 2017): 10451–56. http://dx.doi.org/10.1002/anie.201705315.
Повний текст джерелаTrost, Barry M., Elumalai Gnanamani, and Chao-I. Joey Hung. "Controlling Regioselectivity in the Enantioselective N-Alkylation of Indole Analogues Catalyzed by Dinuclear Zinc-ProPhenol." Angewandte Chemie 129, no. 35 (July 19, 2017): 10587–92. http://dx.doi.org/10.1002/ange.201705315.
Повний текст джерелаLiu, Yanling, Xin Zhou, Deju Shang, Xiaohua Liu, and Xiaoming Feng. "ChemInform Abstract: N,N′-Dioxide-Scandium(III) Complex Catalyzed Highly Enantioselective Friedel-Crafts Alkylation of Indole to Alkylidene Malonates." ChemInform 41, no. 24 (June 15, 2010): no. http://dx.doi.org/10.1002/chin.201024107.
Повний текст джерелаRossi, Sergio, Alessandra Puglisi, Laura Maria Raimondi, and Maurizio Benaglia. "Stereolithography 3D-Printed Catalytically Active Devices in Organic Synthesis." Catalysts 10, no. 1 (January 12, 2020): 109. http://dx.doi.org/10.3390/catal10010109.
Повний текст джерелаJorapur, Yogesh R., Jae Min Jeong, and Dae Yoon Chi. "Potassium carbonate as a base for the N-alkylation of indole and pyrrole in ionic liquids." Tetrahedron Letters 47, no. 14 (April 2006): 2435–38. http://dx.doi.org/10.1016/j.tetlet.2006.01.129.
Повний текст джерелаMino, Takashi, Shingo Komatsu, Kazuya Wakui, Haruka Yamada, Hiroaki Saotome, Masami Sakamoto, and 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, no. 6 (April 2010): 711–18. http://dx.doi.org/10.1016/j.tetasy.2010.03.039.
Повний текст джерелаGallo, Roger, and Mohamed Bourak. "Improving Regioselectivity under Phase Transfer Conditions: Effect of Chemical Parameters and Kinetic Study of Indole N-Alkylation." HETEROCYCLES 31, no. 3 (1990): 447. http://dx.doi.org/10.3987/com-88-4855.
Повний текст джерелаHong, Liang, Wangsheng Sun, Chunxia Liu, Lei Wang, and 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, no. 2 (January 11, 2010): 440–44. http://dx.doi.org/10.1002/chem.200902638.
Повний текст джерелаHong, Liang, Wangsheng Sun, Chunxia Liu, Lei Wang та 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, № 3 (14 січня 2010): 746. http://dx.doi.org/10.1002/chem.201090006.
Повний текст джерелаKuvshinova, Sofya S., Yulia V. Nelyubina, Vladimir A. Larionov, Daria V. Vorobyeva, Sergey N. Osipov та 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 (серпень 2021): 121899. http://dx.doi.org/10.1016/j.jorganchem.2021.121899.
Повний текст джерелаLi, Nai-Kai, Jun-Qi Zhang, Bing-Bing Sun, Hai-Yan Li, and Xing-Wang Wang. "Chiral Diphosphine–Palladium-Catalyzed Sequential Asymmetric Double-Friedel–Crafts Alkylation and N-Hemiketalization for Spiro-polycyclic Indole Derivatives." Organic Letters 19, no. 8 (April 13, 2017): 1954–57. http://dx.doi.org/10.1021/acs.orglett.7b00368.
Повний текст джерелаShi, Yan-Chao, Shou-Guo Wang, Qin Yin, and 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, no. 1 (2014): 39–43. http://dx.doi.org/10.1039/c3qo00008g.
Повний текст джерелаLodeiro, Carlos, Rufina Bastida, Emilia Bértolo, and 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, no. 3 (March 1, 2004): 437–47. http://dx.doi.org/10.1139/v03-214.
Повний текст джерелаHarkov, Stefan. "SYNTHESIS AND CONVERSION OF NEW POTENTIALLY BIOLOGICALLY ACTIVE 4-THIAZOLIDINONE DERIVATIVES WITH A TRIAZINOINDOLE FRAGMENT IN THE MOLECULES." KNOWLEDGE - International Journal 54, no. 4 (September 30, 2022): 677–81. http://dx.doi.org/10.35120/kij5404677h.
Повний текст джерелаWang, Shuai, Yao-Bin Shen, Long-Fei Li, Bin Qiu, Liping Yu, Qing Liu, and 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, no. 22 (November 7, 2019): 8904–8. http://dx.doi.org/10.1021/acs.orglett.9b03011.
Повний текст джерелаBHAGWAT, S. S., and 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, no. 30 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199430115.
Повний текст джерелаBora, Darshana, Stephy Elza John, Mary Sravani Galla, Manda Sathish та 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 (грудень 2022): 112783. http://dx.doi.org/10.1016/j.mcat.2022.112783.
Повний текст джерелаMayer, Szabolcs, András Keglevich, Csilla Sepsey Für, Hedvig Bölcskei, Viktor Ilkei, Péter Keglevich, and László Hazai. "Results in Chemistry of Natural Organic Compounds. Synthesis of New Anticancer Vinca Alkaloids and Flavone Alkaloids." Chemistry 2, no. 3 (August 10, 2020): 714–26. http://dx.doi.org/10.3390/chemistry2030046.
Повний текст джерелаMottinelli, Marco, Mathew P. Leese, and 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 (September 6, 2017): 1871–78. http://dx.doi.org/10.3762/bjoc.13.182.
Повний текст джерелаCrich, David, and 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, no. 2 (June 11, 2010): no. http://dx.doi.org/10.1002/chin.200002192.
Повний текст джерелаLing, Li, Jing Cao, Jianfeng Hu, and Hao Zhang. "Copper-catalyzed N-alkylation of indoles by N-tosylhydrazones." RSC Advances 7, no. 45 (2017): 27974–80. http://dx.doi.org/10.1039/c7ra03765a.
Повний текст джерелаGao, Yadong, Jianhua Li, Songlin Bai, Daoquan Tu, Chao Yang, Zhiwen Ye, Bingcheng Hu, Xiangbing Qi, and Chao Jiang. "Direct synthesis of annulated indoles through palladium-catalyzed double alkylations." Organic Chemistry Frontiers 7, no. 9 (2020): 1149–57. http://dx.doi.org/10.1039/d0qo00135j.
Повний текст джерелаChen, Jian-Ping, Wen-Wen Chen, Yi Li, and 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, no. 11 (2015): 3363–70. http://dx.doi.org/10.1039/c5ob00063g.
Повний текст джерелаSiddiki, S. M. A. Hakim, Kenichi Kon, and Ken-ichi Shimizu. "Selective N-alkylation of indoles with primary alcohols using a Pt/HBEA catalyst." Green Chemistry 17, no. 1 (2015): 173–77. http://dx.doi.org/10.1039/c4gc01419g.
Повний текст джерелаMino, Takashi, Kenji Nishikawa, Moeko Asano, Yamato Shima, Toshibumi Ebisawa, Yasushi Yoshida, and 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, no. 31 (2016): 7509–19. http://dx.doi.org/10.1039/c6ob01354f.
Повний текст джерелаFink, David M. "Cesium Carbonate Promoted N-Alkylation of Indoles." Synlett, no. 13 (2004): 2394–96. http://dx.doi.org/10.1055/s-2004-832836.
Повний текст джерелаZhang, Lvye, Binqiang Wu, Zhangtao Chen, Jinjin Hu, Xiaofei Zeng, and Guofu Zhong. "Chiral phosphoric acid catalyzed enantioselective N-alkylation of indoles with in situ generated cyclic N-acyl ketimines." Chemical Communications 54, no. 66 (2018): 9230–33. http://dx.doi.org/10.1039/c8cc05073b.
Повний текст джерелаHu, Miao, Yong Jiang, Nan Sun, Baoxiang Hu, Zhenlu Shen, Xinquan Hu, and Liqun Jin. "Nickel-catalyzed C3-alkylation of indoles with alcohols via a borrowing hydrogen strategy." New Journal of Chemistry 45, no. 22 (2021): 10057–62. http://dx.doi.org/10.1039/d1nj01581h.
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