Natural Products and Bioprospecting    2015, Vol. 5 Issue (5) : 255-261     DOI: 10.1007/s13659-015-0073-3
Original article |
Total Synthesis of Lignan Lactone(-)-Hinokinin
Qi-Long Zhou1, Hui-Jing Wang1, Pei Tang1, Hao Song2, Yong Qin2
1. Innovative Drug Research Centre, Chongqing University, Chongqing 401331, China;
2. Key Laboratory of Drug Targeting and Drug Delivery Systems of the Ministry of Education, West China School of Pharmacy, Sichuan University, Chengdu 610041, China
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Abstract  This research paper is aimed at studying the total synthesis of pharmacologically active lignan(-)-hinokinin. The synthesis features a three-step cascade reaction involving highly stereoselective Michael addition, anion-oxidative hydroxylation, and oxygen anion cyclization to construct the pivotal butyrolactonimidate intermediate.
Keywords Lignan      Hinokinin      Total synthesis      Cascade reaction     
Fund:We acknowledge grant supports from Chongqing University, and the Fundamental Research Funds for the Central Universities(Project No. 0236015202004).
Issue Date: 11 February 2018
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Qi-Long Zhou,Hui-Jing Wang,Pei Tang, et al. Total Synthesis of Lignan Lactone(-)-Hinokinin[J]. Natural Products and Bioprospecting, 2015, 5(5): 255-261.
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http://npb.kib.ac.cn/EN/10.1007/s13659-015-0073-3     OR     http://npb.kib.ac.cn/EN/Y2015/V5/I5/255
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