Synthesis of D-Glucosamine-Modified Benzo[d][1,2]selenazol-3-(2H)-one Derivatives

Zhongwei Zhang School of Medicine and Pharmacy, Key Laboratory of Marine Drugs, Ministry of Education, Ocean University of China, Qingdao, China

Sumei Ren School of Medicine and Pharmacy, Key Laboratory of Marine Drugs, Ministry of Education, Ocean University of China, Qingdao, China

Shengbiao Wan School of Medicine and Pharmacy, Key Laboratory of Marine Drugs, Ministry of Education, Ocean University of China, Qingdao, China

Wei Li School of Medicine and Pharmacy, Key Laboratory of Marine Drugs, Ministry of Education, Ocean University of China, Qingdao, China

Tao Jiang School of Medicine and Pharmacy, Key Laboratory of Marine Drugs, Ministry of Education, Ocean University of China, Qingdao, ChinaCorrespondence[email protected]

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Yikuan Qi, Chunjun Qin, Shengyong Zhu & Jian Yin. (2023) Chemoselectivity of 3,3'-dithiobis(sulfosuccinimylpropionate)-based 3-mercaptopropionylation of amine-linked aminomonosaccharides. Journal of Carbohydrate Chemistry 42:1-3, pages 59-91.
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Anna Laskowska, Agata J. Pacuła-Miszewska, Magdalena Obieziurska-Fabisiak, Aneta Jastrzębska, Angelika Długosz-Pokorska, Katarzyna Gach-Janczak & Jacek Ścianowski. (2024) Synthesis of New Chiral β-Carbonyl Selenides with Antioxidant and Anticancer Activity Evaluation—Part I. Materials 17:4, pages 899.
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Qing‐Feng Xu‐Xu, Yuji Nishii, Yuta Uetake, Hidehiro Sakurai & Masahiro Miura. (2021) Synthesis of Benzoisoselenazolones via Rh(III)‐Catalyzed Direct Annulative Selenation by Using Elemental Selenium. Chemistry – A European Journal 27:71, pages 17952-17959.
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Hoi‐Ling Seng & Edward R. T. Tiekink. (2012) Anti‐cancer potential of selenium‐ and tellurium‐containing species: opportunities abound!. Applied Organometallic Chemistry 26:12, pages 655-662.
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Krikor Bijian, Zhongwei Zhang, Bin Xu, Su Jie, Bo Chen, Shengbiao Wan, JianHui Wu, Tao Jiang & Moulay A. Alaoui-Jamali. (2012) Synthesis and biological activity of novel organoselenium derivatives targeting multiple kinases and capable of inhibiting cancer progression to metastases. European Journal of Medicinal Chemistry 48, pages 143-152.
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Zhongwei Zhang, Sumei Ren, Shengbiao Wan, Wei Li & Tao Jiang. (2011) ChemInform Abstract: Synthesis of D‐Glucosamine‐Modified Benzo[d][1,2]selenazol‐3‐(2H)‐one Derivatives.. ChemInform 42:16.
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Synthesis of D-Glucosamine-Modified Benzo[d][1,2]selenazol-3-(2H)-one Derivatives

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Synthesis of D-Glucosamine-Modified Benzo[d][1,2]selenazol-3-(2H)-one Derivatives

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