Title of article
Asymmetric synthesis of (−)-4-epi-shikimic acid
Author/Authors
Pornpakakul، نويسنده , , Surachai and Pritchard، نويسنده , , Robin G and Stoodley، نويسنده , , Richard J، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2000
Pages
4
From page
2691
To page
2694
Abstract
The major cycloadduct, arising from the Diels–Alder reaction of maleic anhydride and (1E)-(2′,3′,4′,6′-tetra-O-acetyl-β-d-glucopyranosyloxy)buta-1,3-diene, is converted into methyl 3-O-(β-d-glucopyranosyl)-4-epi-shikimate and into (−)-4-epi-shikimic acid in overall yields of 20 and 17% (based on the diene).
Keywords
asymmetric synthesis , carbohydrates , Diels–Alder reactions , shikimic acid and derivatives , regioselection
Journal title
Tetrahedron Letters
Serial Year
2000
Journal title
Tetrahedron Letters
Record number
1636983
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