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Penicillic acid was isolated from Aspergillus sclerotiorum and converted into 6-iodo-α-pyran-2,5-diones using iodolactonization, a key intermediate for the synthesis of pectinolide F. Structures of penicillic acid and its iodolactonized product were confirmed by using NMR experiments.
Authors are thankful to the director of IIIM Jammu for the encouragement.
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