This work reveals efficient total synthesis of natural products from Salvia miltiorrhiza, highlighting C-H borylation and carbonylation techniques.
Herein we report a divergent strategy culminating in the first total synthesis of five terpene natural products isolated from Salvia miltiorrhiza. This approach features efficient construction of a functionalized tetralin core, a scalable route to a furan coupling partner, and a direct C-H borylation. An operationally simple HFIP-mediated benzylic C-H lactonization allowed late-stage diversification through Pd-catalyzed carbonylation and biaryl coupling, providing concise access to multiple natural products from a common intermediate.
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Strickland et al. (2025) studied this question.
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