Efficient synthesis of (R)-ochratoxin alpha, the key precursor to the mycotoxin ochratoxin A
Two new routes for the synthesis of enantiomerically pure ochratoxin alpha ((3R)-OTα) are presented, which is the key intermediate for the synthesis of ochratoxin A (OTA) by coupling reaction with the amino acid l-phenylalanine. The key step of both routes is the one pot directed ortho-metalation/alkylation/ lactonization of unprotected and suitably functionalized aromatic carboxylic acids, using lithium tetramethylpiperidide (LTMP) and (R)-propylene oxide.
Lenz, Cesar Antonio,Rychlik, Michael
p. 883 - 886
(2013/02/25)
More Articles about upstream products of 1421840-17-6