Streamlined Synthesis of Ellagitannins: Site-Selective Functionalization of the Glucose Core and Stereodivergent Construction of the Hexahydroxydiphenoic Groups

被引:3
作者
Ueda, Yoshihiro [1 ]
Kawabata, Takeo [2 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Interdisciplinary Res Ctr Catalyt Chem, Tsukuba, Ibaraki 3058565, Japan
[2] Int Univ Hlth & Welf, Dept Pharmaceut Sci, Okawa, Fukuoka 8318501, Japan
基金
日本学术振兴会;
关键词
ellagitannin; glucose; site-selective functionalization; stereodivergentreaction; TOTAL CHEMICAL-SYNTHESIS; NONCOVALENT INTERACTIONS; DIMERIC ELLAGITANNIN; PLANT POLYPHENOLS; CHEMISTRY; ACYLATION; INHIBITION; CATALYSTS; TANNINS;
D O I
10.1021/acs.jafc.4c07615
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Ellagitannins are a class of plant polyphenols with a structural diversity of around 1000. Because those with attractive biological activities have been reported, synthetic studies have been performed. The purpose of this perspective is to provide an outlook toward future developments on ellagitannin chemistry and medicinal applications by overviewing synthetic studies. In particular, we summarize recent synthetic efforts of ellagitannins via functionalization of the glucose core and stereodivergent construction of the characteristic hydroxydiphenoic groups. The development of chemical probes utilizing natural ellagitannins is also introduced.
引用
收藏
页码:24191 / 24197
页数:7
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