Total synthesis of 1-oxomiltirone via Suzuki coupling

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Abstract

Abietane diterpenes and miltirone series have shown important activities and for medical purposes in order to achieve the total synthesis of 1-oxomiltrone 1 and miltirone 4, a versatile intermediate 6 was found. The compound 6 could be used as a precursor A-B-C rings with different oxidative degrees in selected abietane diterpenes when synthesized through high yield Suzuki reaction and subsequent cyclization, and total synthesis of 1-oxomiltirone (1) has been achieved. [Figure not available: see fulltext.].

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Li, C. M., Geng, H. C., Li, M. M., Xu, G., Ling, T. J., & Qin, H. B. (2013). Total synthesis of 1-oxomiltirone via Suzuki coupling. Natural Products and Bioprospecting, 3(3), 117–120. https://doi.org/10.1007/s13659-013-0034-7

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