Syntheses of 3-, 4-, and 5-O-feruloylquinic acids

被引：33

作者：

Dokli, Irena ^{[1
]}

Navarini, Luciano ^{[2
]}

Hamersak, Zdenko ^{[1
]}

机构：

[1] Rudjer Boskovic Inst, Div Organ Chem & Biochem, Zagreb 10002, Croatia

[2] Illycaffe Spa, I-34147 Trieste, Italy

来源：

TETRAHEDRON-ASYMMETRY | 2013年 / 24卷 / 13-14期

关键词：

CHLOROGENIC ACIDS; CAFFEINE;

D O I：

10.1016/j.tetasy.2013.06.002

中图分类号：

O61 [无机化学];

学科分类号：

070301 [无机化学];

摘要：

The efficient synthesis of 3-, 4-, and 5-O-feruloylquinic acids starting from D-(-)-quinic acid is described. Esterification of suitably protected quinic acid derivatives with 3-(4-acetoxy-3-methoxyphenyl)-acryloyl chloride and subsequent hydrolysis of all the protecting groups afforded the title products in overall yields of 33%, 15%, and 45%, respectively, (from quinic acid). (C) 2013 Elsevier Ltd. All rights reserved.

引用

页码：785 / 790

页数：6

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