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(¡À)-¦Â-(3,4-Dihydroxyphenyl) lactic acid ((¡À)-DSS) and its derivatives have recently attracted considerable interest due to their potential pharmaceutical activities for anti-oxidation,1 anticoagulance, 2 anti-myocardial ischemia,3 anti-inflammation,4 and anti-neoplasticism.5 Our previous studies6 on distribution and metabolites of Danshen (Salvia miltiorrhiza bunge) and Danshen dripping pills (a patented traditional Chinese medicine consisting of radix salvia miltiorrhizae, radix notoginseng, and borneolum syntheticum) with rabbits suggested that compounds 2 and 3 (Figure 1) might play a key role in the patent medicine of Danshen. Along with studies on the correlation of (¡À)-DSS, (¡À)-IDHP, and (¡À)-DBZ in vivo and their pharmacokinetics and pharmacodynamics, a considerable number of methods to synthesize substituted (¡À)-DSS and their key intermediates7 have been investigated. For example, we developed a synthesis process (Scheme 1),8 which was based on a previously published strategy;9,12 the process involved five steps resulting in an overall yield of only 12%. To improve its yield and avoid using toxic mercury catalysts, an alternative route10 was utilized. However, its overall yield of 18% was also not satisfied for large-scale production. In addition, asymmetric synthesis of IDHP and DBZ was developed by our group,11 but its high cost made it economically not viable for large-scale production. Therefore, there still remain challenges for the production of these derivatives in quality and quantity sufficient for pharmaceutical applications. The aim of the present studies was to develop a pilot-scale synthetic method which can deliver higher yields for the (¡À)-DSS, (¡À)-IDHP, and (¡À)-DBZ production. The use of less toxic catalysts was also investigated for a greener process. Furthermore, we developed a method for chiral separation of (¡À)-IDHP and (¡À)-DBZ to give an optical purity (>99% ee) isomer of R-IDHP, S-IDHP, R-DBZ, and S-DBZ. |
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