Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5275216 | Tetrahedron Letters | 2009 | 4 Pages |
Abstract
An unstable intermediate proepitheaflagallin B (2), a precursor of proepitheaflagallin (3), was isolated as an enzymatic oxidation product of (â)-epigallocatechin (1), and the structure of 2 was determined based on spectroscopic data. The structure and its decomposition revealed that the detailed production mechanism of proepitheaflagallin (3) via a bicyclo[3.2.1]octane-type intermediate was related to that of major black tea pigments, theaflavins.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yosuke Matsuo, Takashi Tanaka, Isao Kouno,