Efficient synthesis of (R)-ochratoxin alpha, the key precursor to the mycotoxin ochratoxin A
2013
Abstract Two new routes for the synthesis of enantiomerically pure ochratoxin alpha ((3 R )-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.
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