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Merck

A new synthetic strategy for catechin-class polyphenols: concise synthesis of (-)-epicatechin and its 3-O-gallate.

Chemical communications (Cambridge, England) (2012-07-14)
Sven Stadlbauer, Ken Ohmori, Fumihiko Hattori, Keisuke Suzuki
RESUMEN

Concise synthesis of (-)-epicatechin and its 3-O-gallate is described, illustrating efficacy of the new strategy for catechin-class polyphenols based on assembly of lithiated fluorobenzene and epoxy alcohol followed by a pyran cyclization. 1,3,5-Trifluorobenzene serves as the A-ring equivalent for functionalization and the pyran annulation.

MATERIALES
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Sigma-Aldrich
1,3,5-Trifluorobenzene, 97%
Sigma-Aldrich
(−)-Epicatechin gallate, ≥98% (HPLC), from green tea
Epicatechin gallate, primary reference standard