| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5167215 | Phytochemistry | 2007 | 8 Pages |
Abstract
Unstable precursors of epigallocatechin-3-O-gallate trimer were isolated after condensation with o-phenylenediamine. The results suggested that oxidative coupling of the galloyl group with the B-ring proceeds by a quinone dimerization mechanism.
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Authors
Yan Li, Takashi Tanaka, Isao Kouno,