Synthesis of a 3,4,5-trimethoxybenzoyl ester analogue of epigallocatechin-3-gallate (EGCG): A potential route to the natural product green tea catechin, EGCG
Nt. Zaveri, Synthesis of a 3,4,5-trimethoxybenzoyl ester analogue of epigallocatechin-3-gallate (EGCG): A potential route to the natural product green tea catechin, EGCG, ORG LETT, 3(6), 2001, pp. 843-846
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The synthesis of a trimethoxybenzoyl ester (D-ring) analogue of epigallocat
echin-3-gallate (EGCG) is described. The versatile synthesis route can be u
sed to synthesize A, B, and D ring analogues of EGCG and involves a key cyc
lization of the chalcone to the 3-flavene. This synthesis provides a possib
le route to the polyphenolic green tea natural product EGCG.