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

Authors
Citation
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
Citations number
61
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANIC LETTERS
ISSN journal
15237060 → ACNP
Volume
3
Issue
6
Year of publication
2001
Pages
843 - 846
Database
ISI
SICI code
1523-7060(20010322)3:6<843:SOA3EA>2.0.ZU;2-9
Abstract
[GRAPHICS] 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.