Synfacts 2011(7): 0707-0707  
DOI: 10.1055/s-0030-1260491
Synthesis of Natural Products and Potential Drugs
© Georg Thieme Verlag Stuttgart ˙ New York

Synthesis of (+)-Lithospermic Acid

Contributor(s): Steven V. Ley, Kimberley A. Roper
D.-H. Wang, J.-Q. Yu*
The Scripps Research Institute, La Jolla, USA
Further Information

Publication History

Publication Date:
17 June 2011 (online)

Significance

(+)-Lithospermic acid was isolated in 1975 from Danshen, a herb traditionally used in the treatment of cardiovascular disorders among other medical conditions, and has recently been shown to have potent, nontoxic anti-HIV activity. The Ellman and Bergman groups completed the first total synthesis using a rhodium-catalyzed C-H activation-hydroarylation sequence (J. Am. Chem. Soc. 2005, 127, 13496). This route uses a rhodium-catalyzed C-H insertion reaction to form the dihydrofuran core, followed by a palladium-catalyzed C-H functionalization to unite the two fragments in a convergent fashion.