Abstract
Natural products with heterocyclic core units are ample and widespread in nature, with many compounds exhibiting promising therapeutic properties. Penipanoid A (1) is a triazole based natural product isolated from the marine sediment derived fungus Penicillium Aneum SD-44 and exhibits the cytotoxicity and antimicrobial activity. Structurally, it features a 1,2,4-triazole motif. Herein, we report an efficient total synthesis of Penipanoid A (1) by a multi-component reaction involving formation of a triazole ring system as the key fragment starting from 4-methoxyphenyl acetic acid. Deprotection of the methoxy protected compound 2 provided the required natural product 1.
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