A convenient one-step gingerol synthesis

被引：25

作者：

Fleming, SA ^{[1
]}

Dyer, CW ^{[1
]}

Eggington, J ^{[1
]}

机构：

[1] Brigham Young Univ, Dept Chem & Biochem, Provo, UT 84602 USA

来源：

SYNTHETIC COMMUNICATIONS | 1999年 / 29卷 / 11期

基金：

美国国家科学基金会;

关键词：

D O I：

10.1080/00397919908086182

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Racemic 6-gingerol can be obtained in a one-pot reaction by hexanal addition to the dianion of zingerone at low temperature. Similarly, addition of octanal or decanal to the dianion provides 8-gingerol or 10-gingerol, respectively. Acid treatment of the gingerols allows for formation of the corresponding shogaols.

引用

页码：1933 / 1939

页数：7

共 12 条

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