Synthesis of Natural Rubrolides B, I, K, L, M, O and Analogues

نویسندگان

چکیده

Abstract The chlorinated natural products, rubrolides B, I, K, L, M and O analogues were synthesized in only five steps employing a robust divergent synthetic strategy. synthesis is performed without using protecting groups starting from key intermediate, which can be commercially available tetronic acid two steps. Selective halogenation vinylogous aldol condensation enable the efficient of highly halogenated occurring as well to build up compound library for antiviral antibiofilm testing. All compounds then tested their activity against influenza A virus strains p H1N1 H3N2 activity. Naturally showed promising activities.

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ژورنال

عنوان ژورنال: European Journal of Organic Chemistry

سال: 2021

ISSN: ['1434-193X', '1099-0690']

DOI: https://doi.org/10.1002/ejoc.202100526