A key intermediate for the synthesis of Tyromycin A, a C‐20 tetrachlorodicarboxylic acid, was produced in six steps starting with the dimerization of methyl 10‐undecenoate which was obtained from a renewable resource, e.g. castor oil. The acyloin condensation product was then oxidized, transformed to the diene, followed by ozonization, chlorination and finally oxidation to the corresponding tetrachlorodicarboxylic acid.
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Steen et al. (2008) studied this question.
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