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First Total Synthesis of Gaylussacin and Its Stilbene Derivatives.

作者信息

Song Injae, Lim Hyewon, Chun Simin, Lee Seok Beom, Huh Jungmoo, Oh Dong-Chan, Hong Suckchang

机构信息

Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.

Natural Products Research Institute, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.

出版信息

J Nat Prod. 2021 Apr 23;84(4):1366-1372. doi: 10.1021/acs.jnatprod.1c00173. Epub 2021 Mar 18.

Abstract

Gaylussacin (), a stilbene glucoside, has been isolated from and is used in Korean folk medicine. Although it was first isolated in 1972, the synthesis of gaylussacin has never been reported. Herein, we report the first total synthesis of gaylussacin in six steps with an overall yield of 23.8%, as well as the synthesis of its derivatives. Structurally, gaylussacin contains a carboxylic acid and a glycoside along with a free phenol on the same benzene ring, making selective functionalization for the synthesis of difficult. Heck cross-coupling was employed as a key step to introduce the stilbene moiety. Glycosylation followed by global deprotection provided natural product .

摘要

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