Total syntheses of anticancer Abietane Diterpenoids, (±)-Royleanone and (±)-Inuroyleanol via Lewis acid catalyzed Hydroarylation

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Abstract

Herein we report a Lewis acid-catalyzed intramolecular hydroarylation strategy enabling an efficient synthesis of [6,6,6]-fused abietane diterpenoids sharing a trans-decalin motif. Using bismuth(III) triflate as an efficient metal triflate, the key intermediates were prepared in high yields, facilitating concise total syntheses of royleanone (1a) and inuroyleanone (1c), showcasing a scalable approach to complex natural product frameworks.

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Kakde, B. N., Noskar, S., Bag, S., & Bisai, A. (2025). Total syntheses of anticancer Abietane Diterpenoids, (±)-Royleanone and (±)-Inuroyleanol via Lewis acid catalyzed Hydroarylation. Tetrahedron Letters, 168. https://doi.org/10.1016/j.tetlet.2025.155715

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