Library construction of stereochemically diverse isomers of spirooliganin: their total synthesis and antiviral activity. Issue 20 (21st April 2021)

• Record Type: Journal Article
• Authors: Wang, Ru-Bing; Ma, Shuang-Gang; Jamieson, Cooper S.; Gao, Rong-Mei; Liu, Yun-Bao; Li, Yong; Wang, Xiao-Jing; Li, Yu-Huan; Houk, Kendall N.; Qu, Jing; Yu, Shi-Shan
• Is Part Of: Chemical science. Volume 12:Issue 20(2021)
• Page Start: 7003
• Page End: 7011
• Publication Date: 2021-04-21
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d1sc01277k
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : Library construction of stereochemically diverse isomers to investigate the relationship between stereoconfiguration and anti-coxsackie virus B3 activity. Abstract : The construction of libraries of stereoisomers of natural products serves as an important approach to investigating the correlation between the stereostructure and biological activity. However, the total synthesis and isomerzation of polycyclic scaffolds with multiple chrial centers are rare. Spirooliganin (1 ), a new skeleton natural product isolated from the plant Illicium oligandrum, was structurally characterized by comprehensive analysis of NMR spectroscopic data and ECD which revealed an unprecedented 5–6–6–6–7 polycyclic framework with six chiral centers. Here we report a 17-step total synthesis to prepare a library of stereochemically diverse isomers of spirooliganin, including 16 diastereoisomers and 16 regioisomers. In addition to a regioselective hetero-Diels–Alder cycloaddition, the synthetic strategy involves a photo-induced stereoselective Diels–Alder reaction, which gives only the abnormal trans -fused product as rationalized by density functional theory calculations. Preliminary biological evaluation showed that spirooliganin and regioisomers 39 exhibited potent inhibition of Coxsackievirus B3. It also revealed the pharmacophore effect of the D-ring (16 R, 18 R, 24 R, and 26 R ) for their antiviral activities.