中文版 | English
Title

Asymmetric synthesis of chiral (thio)chromanes and exploration on their structure-activity relationship in macrophages

Author
Corresponding AuthorWang, Zihao; Wang, Mingfu
Publication Years
2023-10-11
DOI
Source Title
EISSN
2046-2069
Volume13Issue:43
Abstract
["A CuCl/(R,R)-Ph-BPE-catalyzed enantioselective hydroallylation of 2H-chromenes and 2H-thiochromenes with allylic phosphate electrophiles is developed, which enables highly efficient and atom-economical asymmetric access to a series of 4-allyl chromanes and thiochromanes in high yields (up to 91%) with excellent enantioselectivities (up to 99% ee). These valuable chiral chromane and thiochromane products can serve as crucial intermediates for accessing bioactive compounds containing oxygen and sulfur atoms. In addition, the antioxidant and anti-inflammatory effects of various chromanes and thiochromanes were investigated in RAW 264.7 macrophages. The chromanes and thiochromanes exhibited significant inhibitory effects on the production of reactive oxygen species (ROS) and the secretion of pro-inflammatory cytokines, including interleukin-6 (IL-6) and tumor necrosis factor-alpha (TNF-alpha). These findings indicate that the newly synthesized chromanes and thiochromanes hold promise as potential lead compounds for the development of antioxidant and anti-inflammatory drugs.","A CuCl/(R,R)-Ph-BPE-catalyzed enantioselective hydroallylation of 2H-(thio)chromenes is developed, which enables access to a series of 4-allyl (thio)chromanes in high yields (up to 91%) with excellent enantioselectivities (up to 99% ee)."]
URL[Source Record]
Indexed By
Language
English
SUSTech Authorship
Others
Funding Project
This work was supported by Shenzhen Science and Technology Program (ZDSYS20220117155800001), Health@InnoHK Initiative Fund of the Hong Kong Special Administrative Region Government (ITC RC/IHK/4/7), and Shenzhen Basic Research Program for Shenzhen Virtual[ZDSYS20220117155800001] ; Shenzhen Science and Technology Program[ITC RC/IHK/4/7] ; Health@InnoHK Initiative Fund of the Hong Kong Special Administrative Region Government[2021Szvup132]
WOS Research Area
Chemistry
WOS Subject
Chemistry, Multidisciplinary
WOS Accession No
WOS:001083235000001
Publisher
Data Source
Web of Science
Citation statistics
Document TypeJournal Article
Identifierhttp://kc.sustech.edu.cn/handle/2SGJ60CL/582915
DepartmentDepartment of Chemistry
Affiliation
1.Univ Hong Kong, Sch Biol Sci, Hong Kong 999077, Peoples R China
2.Southern Univ Sci & Technol, Dept Chem, Shenzhen 518055, Peoples R China
3.Shenzhen Univ, Inst Adv Study, Shenzhen Key Lab Food Nutr & Hlth, Shenzhen 518060, Peoples R China
4.Hong Kong Baptist Univ, Dept Chem, Hong Kong 999077, Peoples R China
5.Hong Kong Baptist Univ, Sch Chinese Med, Hong Kong 999077, Peoples R China
6.Hong Kong Baptist Univ, Ctr Chinese Herbal Med Drug Dev, Hong Kong 999077, Peoples R China
First Author AffilicationDepartment of Chemistry
Recommended Citation
GB/T 7714
Zhang, Xiao,Zhou, Qian,Zhou, Yue,et al. Asymmetric synthesis of chiral (thio)chromanes and exploration on their structure-activity relationship in macrophages[J]. RSC ADVANCES,2023,13(43).
APA
Zhang, Xiao,Zhou, Qian,Zhou, Yue,Wang, Zihao,Wang, Jun,&Wang, Mingfu.(2023).Asymmetric synthesis of chiral (thio)chromanes and exploration on their structure-activity relationship in macrophages.RSC ADVANCES,13(43).
MLA
Zhang, Xiao,et al."Asymmetric synthesis of chiral (thio)chromanes and exploration on their structure-activity relationship in macrophages".RSC ADVANCES 13.43(2023).
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