318949-09-6Relevant articles and documents
Methods in synthesis of flavonoids. Part 2: High yield access to both enantiomers of catechin
Nay,Monti,Nuhrich,Deffieux,Merillon,Vercauteren
, p. 9049 - 9051 (2000)
Resolution of racemic synthetic tetra-O-benzylcatechin 2 is described, through the formation of esters S and 6 derived from dibenzoyl-L-tartaric acid. The diastereoisomer of the natural series 6 was separated by crystallization, the other one being an oil. This process allowed us to prepare enantiomerically pure (+)-catechin 8 in high yield. The pure isomer in the ent-series 9 could be obtained, following the same scheme of reactions. (C) 2000 Elsevier Science Ltd.