Статті в журналах з теми "3-disubstituted oxindoles"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "3-disubstituted oxindoles".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.
Ortega-Martínez, Aitor, Cynthia Molina, Cristina Moreno-Cabrerizo, José Sansano, and Carmen Nájera. "Synthesis of 3,3-Disubstituted 2-Oxindoles by Deacylative Alkylation of 3-Acetyl-2-oxindoles." Synthesis 49, no. 23 (August 22, 2017): 5203–10. http://dx.doi.org/10.1055/s-0036-1590880.
Повний текст джерелаCui, Bao-Dong, Yong You, Jian-Qiang Zhao, Jian Zuo, Zhi-Jun Wu, Xiao-Ying Xu, Xiao-Mei Zhang, and Wei-Cheng Yuan. "3-Pyrrolyl-oxindoles as efficient nucleophiles for organocatalytic asymmetric synthesis of structurally diverse 3,3′-disubstituted oxindole derivatives." Chemical Communications 51, no. 4 (2015): 757–60. http://dx.doi.org/10.1039/c4cc08364d.
Повний текст джерелаDing, Zhengtian, and Wangqing Kong. "Synthesis of Carbonyl-Containing Oxindoles via Ni-Catalyzed Reductive Aryl-Acylation and Aryl-Esterification of Alkenes." Molecules 27, no. 18 (September 11, 2022): 5899. http://dx.doi.org/10.3390/molecules27185899.
Повний текст джерелаChen, Lin, Yong You, Ming-Liang Zhang, Jian-qiang Zhao, Jian Zuo, Xiao-Mei Zhang, Wei-Cheng Yuan та Xiao-Ying Xu. "Organocatalytic asymmetric Michael addition of 3-substituted oxindoles to α,β-unsaturated acyl phosphonates for the synthesis of 3,3′-disubstituted oxindoles with chiral squaramides". Organic & Biomolecular Chemistry 13, № 15 (2015): 4413–17. http://dx.doi.org/10.1039/c5ob00317b.
Повний текст джерелаCheng, Wen-Fu, Ling-Yan Chen, Fang-Fang Xu, Wei-Yu Lin, Xinfeng Ren, and Ya Li. "Organocatalytic asymmetric Michael addition between 3-subsituted oxindoles and enals catalyzed by camphor sulfonyl hydrazine." Organic & Biomolecular Chemistry 17, no. 4 (2019): 885–91. http://dx.doi.org/10.1039/c8ob02934b.
Повний текст джерелаRao, Madhuri P., Shubha S. Gunaga, Johannes Zuegg, Rambabu Pamarthi та Madhu Ganesh. "Highly regio- and diastereoselective [3 + 2]-cycloadditions involving indolediones and α,β-disubstituted nitroethylenes". Organic & Biomolecular Chemistry 17, № 42 (2019): 9390–402. http://dx.doi.org/10.1039/c9ob01429b.
Повний текст джерелаZhang, Chun-Lin, You-Feng Han та Song Ye. "N-Heterocyclic carbene-catalyzed β-addition of enals to 3-alkylenyloxindoles: synthesis of oxindoles with all-carbon quaternary stereocenters". Chemical Communications 55, № 55 (2019): 7966–69. http://dx.doi.org/10.1039/c9cc03099a.
Повний текст джерелаKrishnan, Shyam, and Brian M. Stoltz. "Preparation of 3,3-disubstituted oxindoles by addition of malonates to 3-halo-3-oxindoles." Tetrahedron Letters 48, no. 43 (October 2007): 7571–73. http://dx.doi.org/10.1016/j.tetlet.2007.08.131.
Повний текст джерелаLi, Man, Fu-Sheng He, Long-Shan Ji, Ya-Ting Gao, Xin Zhang, Zhuo Yu, Miao Fang, Jie Wu, and Yue-Qiu Gao. "Synthesis and biological evaluation of fluorinated 3,4-dihydroquinolin-2(1H)-ones and 2-oxindoles for anti-hepatic fibrosis." RSC Advances 11, no. 11 (2021): 5923–27. http://dx.doi.org/10.1039/d0ra09430g.
Повний текст джерелаCao, An-Zhu, Yu-Ting Xiao, Yan-Chen Wu, Ren-Jie Song, Ye-Xiang Xie та Jin-Heng Li. "Copper-catalyzed C–H [3 + 2] annulation of N-substituted anilines with α-carbonyl alkyl bromides via C(sp3)–Br/C(sp2)–H functionalization". Organic & Biomolecular Chemistry 18, № 11 (2020): 2170–74. http://dx.doi.org/10.1039/d0ob00399a.
Повний текст джерелаXu, Lubin, Haohua Chen, Jian Liu, Lan Zhou, Qing Liu, Yu Lan, and Jian Xiao. "Chiral phosphoric acid-catalyzed asymmetric C(sp3)–H functionalization of biomass-derived 2,5-dimethylfuran via two sequential Cope-type rearrangements." Organic Chemistry Frontiers 6, no. 8 (2019): 1162–67. http://dx.doi.org/10.1039/c8qo01375f.
Повний текст джерелаLiu, Yong-Liang, Xiao-Ping Wang, Jie Wei, and Ya Li. "Synthesis of oxindoles bearing a stereogenic 3-fluorinated carbon center from 3-fluorooxindoles." Organic & Biomolecular Chemistry 20, no. 3 (2022): 538–52. http://dx.doi.org/10.1039/d1ob01964c.
Повний текст джерелаWang, Juanjuan, Danfeng Huang, Ke-Hu Wang, Xiansha Peng, Yingpeng Su, Yulai Hu, and Ying Fu. "Tin powder-promoted one-pot synthesis of 3-spiro-fused or 3,3′-disubstituted 2-oxindoles." Organic & Biomolecular Chemistry 14, no. 40 (2016): 9533–42. http://dx.doi.org/10.1039/c6ob01487a.
Повний текст джерелаNakazaki, Atsuo, Keitaro Miyagawa, and Toshio Nishikawa. "Diastereoselective Synthesis of 3,3-Disubstituted Oxindoles from N-Aryl-3-Chlorooxindoles Bearing C–N Axial Chirality via Nucleophilic Substitution." Synlett 26, no. 08 (February 24, 2015): 1116–20. http://dx.doi.org/10.1055/s-0034-1380266.
Повний текст джерелаDevi, Manju, Amol P. Jadhav, and Ravi P. Singh. "KOH-mediated stereoselective alkylation of 3-bromooxindoles for the synthesis of 3,3′-disubstituted oxindoles with two contiguous all carbon quaternary centres." New Journal of Chemistry 45, no. 19 (2021): 8445–48. http://dx.doi.org/10.1039/d0nj06283a.
Повний текст джерелаDeng, Fei, Shin A. Moteki, and Keiji Maruoka. "Catalytic Asymmetric Alkylation of 3-Aryl-Substituted Oxindoles to give 3,3-Disubstituted Oxindoles under Phase-Transfer Conditions." Asian Journal of Organic Chemistry 3, no. 4 (March 12, 2014): 395–98. http://dx.doi.org/10.1002/ajoc.201400011.
Повний текст джерелаFeng, Ting-Ting, Xuan Huang, Xiong-Li Liu, De-Hong Jing, Xiong-Wei Liu, Feng-Ming Guo, Ying Zhou, and Wei-Cheng Yuan. "Highly regioselective synthesis of 3-alkenyl-oxindole ring-fused 3,3′-disubstituted oxindoles via direct gamma-substitution of Morita–Baylis–Hillman carbonates of isatins with 3-substituted oxindoles." Org. Biomol. Chem. 12, no. 46 (October 2, 2014): 9366–74. http://dx.doi.org/10.1039/c4ob01523a.
Повний текст джерелаMeerakrishna, Ramakrishnan Suseela, Suresh Snoxma Smile, Mohanakumaran Athira, Venkata Surya Kumar Choutipalli, and Ponnusamy Shanmugam. "Diverse reactivity of isatin-based N,N′-cyclic azomethine imine dipoles with arynes: synthesis of 1′-methyl-2′-oxospiro [indene-1,3′-indolines] and 3-aryl-3-pyrazol-2-oxindoles." New Journal of Chemistry 44, no. 27 (2020): 11593–601. http://dx.doi.org/10.1039/d0nj01684e.
Повний текст джерелаDeng, Fei, Shin A. Moteki, and Keiji Maruoka. "ChemInform Abstract: Catalytic Asymmetric Alkylation of 3-Aryl-Substituted Oxindoles to Give 3,3-Disubstituted Oxindoles under Phase-Transfer Conditions." ChemInform 45, no. 45 (October 23, 2014): no. http://dx.doi.org/10.1002/chin.201445125.
Повний текст джерелаCui, Bao-Dong, Yong You, Jian-Qiang Zhao, Jian Zuo, Zhi-Jun Wu, Xiao-Ying Xu, Xiao-Mei Zhang, and Wei-Cheng Yuan. "ChemInform Abstract: 3-Pyrrolyl-Oxindoles as Efficient Nucleophiles for Organocatalytic Asymmetric Synthesis of Structurally Diverse 3,3′-Disubstituted Oxindole Derivatives." ChemInform 46, no. 23 (May 22, 2015): no. http://dx.doi.org/10.1002/chin.201523124.
Повний текст джерелаZuo, Jian, Zhi-Jun Wu, Jian-Qiang Zhao, Ming-Qiang Zhou, Xiao-Ying Xu, Xiao-Mei Zhang, and Wei-Cheng Yuan. "Preparation of 3-Sulfonylated 3,3-Disubstituted Oxindoles by the Addition of Sulfinate Salts to 3-Halooxindoles." Journal of Organic Chemistry 80, no. 1 (December 8, 2014): 634–40. http://dx.doi.org/10.1021/jo502270a.
Повний текст джерелаSong, Xiang-Jia, Hong-Xia Ren, Min Xiang, Chen-Yi Li, Ying Zou, Xia Li, Zhi-Cheng Huang, Fang Tian та Li-Xin Wang. "Organocatalytic Enantioselective Michael Addition between 3-(3-hydroxy-1H-pyrazol-1-yl)Oxindole and β-Nitrostyrene for the Preparation of Chiral Disubstituted Oxindoles". Journal of Organic Chemistry 85, № 14 (25 червня 2020): 9290–300. http://dx.doi.org/10.1021/acs.joc.9b03337.
Повний текст джерелаKaur, Jasneet, Anita Kumari, and Swapandeep Singh Chimni. "Grinding assisted, column chromatography free decarboxylative carbon-carbon bond formation: Greener synthesis of 3, 3-disubstituted oxindoles." Tetrahedron 73, no. 6 (February 2017): 802–8. http://dx.doi.org/10.1016/j.tet.2016.12.070.
Повний текст джерелаLee, Hyun Ju, Ko Hoon Kim, Se Hee Kim, and Jae Nyoung Kim. "Palladium-catalyzed oxidative arylation of trisubstituted olefin: an efficient synthesis of 3-(disubstituted)alkylidene-oxindoles." Tetrahedron Letters 54, no. 2 (January 2013): 170–75. http://dx.doi.org/10.1016/j.tetlet.2012.10.122.
Повний текст джерелаJia, Shi-Kun, Long-Long Song, Yu-Bing Lei, A. Gopi Krishna Reddy, Dong Xing, and Wen-Hao Hu. "A Rh(ii)-catalyzed three-component reaction of 3-diazooxindoles with N,N-disubstituted anilines and glyoxylates for the synthesis of 3-aryl-3-substituted oxindoles." Organic & Biomolecular Chemistry 14, no. 43 (2016): 10157–60. http://dx.doi.org/10.1039/c6ob01907b.
Повний текст джерелаZuo, Jian, Zhi-Jun Wu, Jian-Qiang Zhao, Ming-Qiang Zhou, Xiao-Ying Xu, Xiao-Mei Zhang, and Wei-Cheng Yuan. "ChemInform Abstract: Preparation of 3-Sulfonylated 3,3-Disubstituted Oxindoles by the Addition of Sulfinate Salts to 3-Halooxindoles." ChemInform 46, no. 22 (May 15, 2015): no. http://dx.doi.org/10.1002/chin.201522152.
Повний текст джерелаYou, Yong, Zhi-Jun Wu, Zhen-Hua Wang, Xiao-Ying Xu, Xiao-Mei Zhang, and Wei-Cheng Yuan. "Enantioselective Synthesis of 3,3-Disubstituted Oxindoles Bearing Two Different Heteroatoms at the C3 Position by Organocatalyzed Sulfenylation and Selenenylation of 3-Pyrrolyl-oxindoles." Journal of Organic Chemistry 80, no. 16 (August 12, 2015): 8470–77. http://dx.doi.org/10.1021/acs.joc.5b01491.
Повний текст джерелаWu, Chongyang, Guofeng Li, Wangsheng Sun, Ming Zhang, Liang Hong, and Rui Wang. "Organocatalytic Highly Enantioselective Monofluoroalkylation of 3-Bromooxindoles: Construction of Fluorinated 3,3′-Disubstituted Oxindoles and Their Derivatives." Organic Letters 16, no. 7 (March 18, 2014): 1960–63. http://dx.doi.org/10.1021/ol500517d.
Повний текст джерелаKim, Ko Hoon, Hye Ran Moon, Junseong Lee та Jae Nyoung Kim. "Palladium-Catalyzed Construction of Spirooxindoles by Arylative Cyclization of 3-(γ,δ-Disubstituted)allylidene-2-Oxindoles". Advanced Synthesis & Catalysis 357, № 4 (4 лютого 2015): 701–8. http://dx.doi.org/10.1002/adsc.201400965.
Повний текст джерелаLee, Hyun Ju, Ko Hoon Kim, Se Hee Kim, and Jae Nyoung Kim. "ChemInform Abstract: Palladium-Catalyzed Oxidative Arylation of Trisubstituted Olefin: An Efficient Synthesis of 3-(Disubstituted)alkylidene-oxindoles." ChemInform 44, no. 15 (March 25, 2013): no. http://dx.doi.org/10.1002/chin.201315107.
Повний текст джерелаKókai, Eszter, Gyula Simig, and Balázs Volk. "Literature Survey and Further Studies on the 3-Alkylation of N-Unprotected 3-Monosubstituted Oxindoles. Practical Synthesis of N-Unprotected 3,3-Disubstituted Oxindoles and Subsequent Transformations on the Aromatic Ring." Molecules 22, no. 1 (December 26, 2016): 24. http://dx.doi.org/10.3390/molecules22010024.
Повний текст джерелаChen, Lin, Yong You, Ming-Liang Zhang, Jian-qiang Zhao, Jian Zuo, Xiao-Mei Zhang, Wei-Cheng Yuan та Xiao-Ying Xu. "ChemInform Abstract: Organocatalytic Asymmetric Michael Addition of 3-Substituted Oxindoles to α,β-Unsaturated Acyl Phosphonates for the Synthesis of 3,3′-Disubstituted Oxindoles with Chiral Squaramides." ChemInform 46, № 34 (серпень 2015): no. http://dx.doi.org/10.1002/chin.201534147.
Повний текст джерелаPathan, Mohsinkhan Y., Santosh S. Chavan, Taufeekaslam M. Y. Shaikh, Shridhar H. Thorat, Rajesh G. Gonnade, and Shafeek A. R. Mulla. "Facile One-Pot Multi-Component Synthesis of Spirooxindoles and 3, 3’-Disubstituted Oxindoles via sp3 C-H Activation/Functionalization of Azaarenes." ChemistrySelect 2, no. 28 (September 29, 2017): 9147–52. http://dx.doi.org/10.1002/slct.201701507.
Повний текст джерелаZuo, Jian, Yu-Hua Liao, Xiao-Mei Zhang та Wei-Cheng Yuan. "Organocatalyzed Enantioselective Decarboxylative Stereoablation Reaction for the Construction of 3,3′-Disubstituted Oxindoles Using β-Ketoacids and 3-Halooxindoles". Journal of Organic Chemistry 77, № 24 (7 грудня 2012): 11325–32. http://dx.doi.org/10.1021/jo302048v.
Повний текст джерелаKim, Ko Hoon, Hye Ran Moon, Junseong Lee та Jae Nyoung Kim. "ChemInform Abstract: Palladium-Catalyzed Construction of Spirooxindoles by Arylative Cyclization of 3-(γ,δ-Disubstituted)allylidene-2-Oxindoles." ChemInform 46, № 31 (16 липня 2015): no. http://dx.doi.org/10.1002/chin.201531140.
Повний текст джерелаWu, Chongyang, Guofeng Li, Wangsheng Sun, Ming Zhang, Liang Hong, and Rui Wang. "ChemInform Abstract: Organocatalytic Highly Enantioselective Monofluoroalkylation of 3-Bromooxindoles: Construction of Fluorinated 3,3′-Disubstituted Oxindoles and Their Derivatives." ChemInform 45, no. 37 (August 28, 2014): no. http://dx.doi.org/10.1002/chin.201437132.
Повний текст джерелаLiu, Xiong-Wei, Zhen Yao, Guan-Lian Wang, Zhi-Yong Chen, Xiong-Li Liu, Min-Yi Tian, Qi-Di Wei, Ying Zhou, and Jian-Fei Zhang. "Efficient 1,6-addition reactions of 3-substituted oxindoles: Access to isoxazole-fused 3,3′-disubstituted oxindole scaffolds and hexahydro-1h-pyrido[2,3-b]indol-2-one scaffolds." Synthetic Communications 48, no. 12 (May 23, 2018): 1454–64. http://dx.doi.org/10.1080/00397911.2018.1454475.
Повний текст джерелаZhou, Rong, Rongfang Liu, Kai Zhang, Ling Han, Honghui Zhang, Wenchao Gao та Ruifeng Li. "Metal-free formal carbon–halogen bond insertion: facile syntheses of 3-halo 3,3′-disubstituted oxindoles and spirooxindole-γ-butyrolactones". Chemical Communications 53, № 51 (2017): 6860–63. http://dx.doi.org/10.1039/c7cc03765a.
Повний текст джерелаMoon, Hye Ran, Ko Hoon Kim, Junseong Lee та Jae Nyoung Kim. "Synthesis of 3-(γ,δ-Disubstituted)allylidene-2-Oxindoles from Isatins by Wittig Reaction with Morita-Baylis-Hillman Bromides". Bulletin of the Korean Chemical Society 36, № 1 (січень 2015): 219–25. http://dx.doi.org/10.1002/bkcs.10053.
Повний текст джерелаOhmatsu, Kohsuke, Yuichiro Ando, and Takashi Ooi. "Asymmetric Substitution at the Tetrasubstituted Chiral Carbon: Catalytic Ring-Opening Alkylation of Racemic 2,2-Disubstituted Aziridines with 3-Substituted Oxindoles." Journal of the American Chemical Society 135, no. 50 (December 10, 2013): 18706–9. http://dx.doi.org/10.1021/ja411647x.
Повний текст джерелаWang, Dong-Chao, Hai-Xia Wang, Er-Jun Hao, Xiao-Han Jiang, Ming-Sheng Xie, Gui-Rong Qu, and Hai-Ming Guo. "Synthesis of 3,3-Disubstituted Oxindoles Containing a 3-(4-Aminobut-2-ynyl) Unit via Domino Heck-Sonogashira Reaction in Water." Advanced Synthesis & Catalysis 358, no. 3 (January 18, 2016): 494–99. http://dx.doi.org/10.1002/adsc.201500887.
Повний текст джерелаZuo, Jian, Yu-Hua Liao, Xiao-Mei Zhang та Wei-Cheng Yuan. "ChemInform Abstract: Organocatalyzed Enantioselective Decarboxylative Stereoablation Reaction for the Construction of 3,3′-Disubstituted Oxindoles Using β-Ketoacids and 3-Halooxindoles." ChemInform 44, № 22 (13 травня 2013): no. http://dx.doi.org/10.1002/chin.201322114.
Повний текст джерелаYou, Yong, Zhi-Jun Wu, Jian-Feng Chen, Zhen-Hua Wang, Xiao-Ying Xu, Xiao-Mei Zhang та Wei-Cheng Yuan. "Organocatalytic Asymmetric Michael Addition of 3-Pyrrolyloxindoles to β-Phthalimidonitroethene for the Synthesis of 3,3′-Disubstituted Oxindoles Bearing Contiguous 3,α,β-Triamino Functionality". Journal of Organic Chemistry 81, № 13 (17 червня 2016): 5759–65. http://dx.doi.org/10.1021/acs.joc.6b00896.
Повний текст джерелаMORENO-CABRERIZO, CRISTINA, AITOR ORTEGA-MARTÍNEZ, CYNTHIA MOLINA, CARMEN NÁJERA, and JOSÉ M. SANSANO. "Deacylative alkylation (DaA) of N-methyl-3-acetyl-2-oxindole for the synthesis of symmetrically 3,3-disubstituted 2-oxindoles. An access gate to anticancer agents and natural products." Anais da Academia Brasileira de Ciências 90, no. 1 suppl 2 (2018): 1089–99. http://dx.doi.org/10.1590/0001-3765201820170783.
Повний текст джерелаOhmatsu, Kohsuke, Yuichiro Ando, and Takashi Ooi. "ChemInform Abstract: Asymmetric Substitution at the Tetrasubstituted Chiral Carbon: Catalytic Ring-Opening Alkylation of Racemic 2,2-Disubstituted Aziridines with 3-Substituted Oxindoles." ChemInform 45, no. 27 (June 20, 2014): no. http://dx.doi.org/10.1002/chin.201427114.
Повний текст джерелаWang, Dong-Chao, Hai-Xia Wang, Er-Jun Hao, Xiao-Han Jiang, Ming-Sheng Xie, Gui-Rong Qu, and Hai-Ming Guo. "Cover Picture: Synthesis of 3,3-Disubstituted Oxindoles Containing a 3-(4-Aminobut-2-ynyl) Unit via Domino Heck-Sonogashira Reaction in Water (Adv. Synth. Catal. 3/2016)." Advanced Synthesis & Catalysis 358, no. 3 (February 2, 2016): 506. http://dx.doi.org/10.1002/adsc.201600052.
Повний текст джерелаWang, Xiaogang, Jin Zhang, Yuan He, Di Chen, Chao Wang, Fangzhou Yang, Weitao Wang, Yangmin Ma та Michal Szostak. "Ruthenium(II)-Catalyzed Ortho-C–H Alkylation of Naphthylamines with Diazo Compounds for Synthesis of 2,2-Disubstituted π-Extended 3-Oxindoles in Water". Organic Letters 22, № 13 (19 червня 2020): 5187–92. http://dx.doi.org/10.1021/acs.orglett.0c01811.
Повний текст джерелаPiemontesi, Cyril, Qian Wang, and Jieping Zhu. "Synthesis of 3,3-disubstituted oxindoles by one-pot integrated Brønsted base-catalyzed trichloroacetimidation of 3-hydroxyoxindoles and Brønsted acid-catalyzed nucleophilic substitution reaction." Organic & Biomolecular Chemistry 11, no. 9 (2013): 1533. http://dx.doi.org/10.1039/c2ob27196f.
Повний текст джерелаPiemontesi, Cyril, Qian Wang, and Jieping Zhu. "ChemInform Abstract: Synthesis of 3,3-Disubstituted Oxindoles by One-Pot Integrated Broensted Base-Catalyzed Trichloroacetimidation of 3-Hydroxyoxindoles and Broensted Acid-Catalyzed Nucleophilic Substitution Reaction." ChemInform 44, no. 29 (July 1, 2013): no. http://dx.doi.org/10.1002/chin.201329113.
Повний текст джерелаKim, Su Yeon, Sangku Lee, Gieun Kim, Beom Kyu Min та Jae Nyoung Kim. "Synthesis of 3-(β,δ-Disubstituted)allylidene-2-oxindoles by SN 2′ Reaction of Phosphorous Ylides with Carbonates of Isatin-derived Moritas-Baylis-Hillman Adducts". Bulletin of the Korean Chemical Society 38, № 9 (21 липня 2017): 1097–100. http://dx.doi.org/10.1002/bkcs.11193.
Повний текст джерела