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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 44, 2014 - Issue 15
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Original Articles

Metal-Free–Catalyzed Oxidative Trimerization of Indoles Using NaNO2 to Construct Quaternary Carbon Centers: Synthesis of 2-(1H-Indol-3-yl)-2,3′-biindolin-3-ones

Jun Xue Department of Chemistry and Chemical Engineering, Gannan Normal University, Ganzhou, Jiangxi, China
,
Yunhong Bao Department of Chemistry and Chemical Engineering, Gannan Normal University, Ganzhou, Jiangxi, China
,
Wenbing Qin Department of Chemistry and Chemical Engineering, Gannan Normal University, Ganzhou, Jiangxi, China
,
Jiayi Zhu Department of Chemistry and Chemical Engineering, Gannan Normal University, Ganzhou, Jiangxi, China
,
Yubo Kong Department of Chemistry and Chemical Engineering, Gannan Normal University, Ganzhou, Jiangxi, China
,
Hongen Qu Department of Chemistry and Chemical Engineering, Gannan Normal University, Ganzhou, Jiangxi, China
,
Zhengwang Chen Department of Chemistry and Chemical Engineering, Gannan Normal University, Ganzhou, Jiangxi, China
&
Liangxian Liu Department of Chemistry and Chemical Engineering, Gannan Normal University, Ganzhou, Jiangxi, ChinaCorrespondence[email protected]
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Pages 2215-2221 | Received 15 Sep 2013, Published online: 06 Jun 2014

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Ankita Khataniar, Abhichandan Das, Manash J Baruah, Kusum K Bania, Sanchaita Rajkhowa, Sami A Al-Hussain & Magdi EA Zaki. (2023) An Integrative Approach to Study the Inhibition of Providencia vermicola FabD Using C2-Quaternary Indolinones. Drug Design, Development and Therapy 17, pages 3325-3347.
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Articles from other publishers (10)

Airu Hashidoko, Taku Kitanosono, Yasuhiro Yamashita & Shū Kobayashi. (2024) Water vs. Organic Solvents: Water‐Controlled Divergent Reactivity of 2‐Substituted Indoles. Chemistry – An Asian Journal 19:5.
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Ballanki Trinadh & Baby Viswambharan. (2023) Potassium persulfate mediated oxidative dearomatization and C–H functionalization of indoles in water: Green and transition metal free approach for the synthesis of indolone derivatives. Tetrahedron 142, pages 133527.
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Yu Dong, Jun-Hu Qian, Xiang-Long Chen, Hui Jiang, Xue Li, Qiang Zhou, Ting Mei, Zhi-Chuan Shi, Zhong-Hui Li & Bing He. (2022) Metal-free synthesis of C2-quaternary indolinones by (NH 4 ) 2 S 2 O 8 mediated oxidative dearomatization of indoles . RSC Advances 12:33, pages 21022-21025.
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Manash J. Baruah, Anurag Dutta, Subir Biswas, Gautam Gogoi, Nazimul Hoque, Pradip K. Bhattacharyya & Kusum K. Bania. (2022) Fe 2 O 3 Nanocatalysts Supported on Zeolite-Y for the Selective Synthesis of C2 Di-Indolyl Indolones and Isatins . ACS Applied Nano Materials 5:1, pages 1446-1459.
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Li-Ting Cheng, Sheng-Qi Luo, Bor-Cherng Hong, Chia-Ling Chen, Wen-Shan Li & Gene-Hsiang Lee. (2020) Oxidative trimerization of indoles via water-assisted visible-light photoredox catalysis and the study of their anti-cancer activities . Organic & Biomolecular Chemistry 18:32, pages 6247-6252.
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Gaurav Shukla, Anjali Dahiya, Tipu Alam & Bhisma K. Patel. (2019) Visible Light‐Mediated C2‐Quaternarization of N‐Alkyl Indoles through Oxidative Dearomatization using Ir(III) Catalyst. Asian Journal of Organic Chemistry 8:12, pages 2243-2248.
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Sushobhan Mukhopadhyay & Sanjay Batra. (2019) Applications of Sodium Nitrite in Organic Synthesis. European Journal of Organic Chemistry 2019:38, pages 6424-6451.
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Xinpeng Jiang, Bingbin Zhu, Kai Lin, Guan Wang, Wei-Ke Su & Chuanming Yu. (2019) Metal-free synthesis of 2,2-disubstituted indolin-3-ones. Organic & Biomolecular Chemistry 17:8, pages 2199-2203.
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Bhaskar Deka, Mohit L. Deb, Ranjit Thakuria & Pranjal K. Baruah. (2018) I2/TBHP/cyclohexanone a novel catalyst system for the oxidative dearomatization of indoles to indolin-3-ones at room temperature under solvent-free condition. Catalysis Communications 106, pages 68-72.
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Jun Xue, Yunhong Bao, Wenbing Qin, Jiayi Zhu, Yubo Kong, Hongen Qu, Zhengwang Chen & Liangxian Liu. (2014) ChemInform Abstract: Metal‐Free‐Catalyzed Oxidative Trimerization of Indoles Using NaNO 2 to Construct Quaternary Carbon Centers: Synthesis of 2‐(1H‐Indol‐3‐yl)‐2,3′‐biindolin‐3‐ones. . ChemInform 45:49.
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