应用天然产物 ›› 2015, Vol. 5 ›› Issue (5): 255-261.DOI: 10.1007/s13659-015-0073-3
Qi-Long Zhou1, Hui-Jing Wang1, Pei Tang1, Hao Song2, Yong Qin2
收稿日期:
2015-09-03
修回日期:
2015-09-22
出版日期:
2015-10-24
发布日期:
2018-02-11
通讯作者:
Pei Tang,e-mail:tangpei@cqu.edu.cn;Yong Qin,e-mail:yongqin@scu.edu.cn
基金资助:
Qi-Long Zhou1, Hui-Jing Wang1, Pei Tang1, Hao Song2, Yong Qin2
Received:
2015-09-03
Revised:
2015-09-22
Online:
2015-10-24
Published:
2018-02-11
Supported by:
摘要: 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.
Qi-Long Zhou, Hui-Jing Wang, Pei Tang, Hao Song, Yong Qin. Total Synthesis of Lignan Lactone(-)-Hinokinin[J]. 应用天然产物, 2015, 5(5): 255-261.
Qi-Long Zhou, Hui-Jing Wang, Pei Tang, Hao Song, Yong Qin. Total Synthesis of Lignan Lactone(-)-Hinokinin[J]. Natural Products and Bioprospecting, 2015, 5(5): 255-261.
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