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Original Articles

Total synthesis of 6′-hydroxyjusticidin A

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Pages 322-326 | Received 18 Jul 2011, Accepted 22 Dec 2011, Published online: 01 Mar 2012

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Sheng-Peng Wang, Yuan-Feng Tong, Li Li, Song Wu & Yan Qi. (2013) The synthesis of justicidinoside B and its atropisomer. Journal of Asian Natural Products Research 15:6, pages 644-649.
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Articles from other publishers (6)

Kai Wei, Yucui Sun, Yiren Xu, Wen Hu, Ying Ma, Yi Lu, Wen Chen & Hongbin Zhang. (2022) Total synthesis of justicidin B, justicidin E, and taiwanin C: A general and flexible approach toward the synthesis of natural arylnaphthalene lactone lignans. Frontiers in Chemistry 10.
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Cetin Bayrak, Gulsah Yildizhan, Namik Kilinc, Serdar Durdagi & Abdullah Menzek. (2021) Synthesis and Aldose Reductase Inhibition Effects of Novel N ‐Benzyl‐4‐Methoxyaniline Derivatives . Chemistry & Biodiversity 19:1.
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Yang Zhao, Chuen-Fai Ku, Xin-Ya Xu, Nga-Yi Tsang, Yu Zhu, Chen-Liang Zhao, Kang-Lun Liu, Chuang-Chuang Li, Lijun Rong & Hong-Jie Zhang. (2021) Stable Axially Chiral Isomers of Arylnaphthalene Lignan Glycosides with Antiviral Potential Discovered from Justicia procumbens . The Journal of Organic Chemistry 86:8, pages 5568-5583.
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Bharti Rajesh Kumar Shyamlal, Lalit Yadav, Mohit K. Tiwari, Manas Mathur, Jaroslav I. Prikhodko, Irina V. Mashevskaya, Dharmendra K. Yadav & Sandeep Chaudhary. (2020) Synthesis, Bioevaluation, Structure-Activity Relationship and Docking Studies of Natural Product Inspired (Z)-3-benzylideneisobenzofuran-1(3H)-ones as Highly Potent antioxidants and Antiplatelet agents. Scientific Reports 10:1.
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Dipakranjan Mal & Joyeeta Roy. (2015) A regioselective facile synthesis of furo[3,4-b]carbazolones: application to the total synthesis of mafaicheenamine E and claulansine D. Org. Biomol. Chem. 13:22, pages 6344-6352.
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Sheng-Peng Wang, Yuan-Feng Tong, Dong-Mei Wang, Nan Wang, Zheng Yan, Ping Huang & Song Wu. (2014) Synthesis and cytotoxicity evaluation of a novel justicidin G analogue and its phosphate ester. Chinese Chemical Letters 25:7, pages 1044-1046.
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