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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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ĿǰµÄÑо¿Ä¿±êÊÇ¿ª·¢Ò»ÖÖÄÜÖÐÊÔ¹æÄ£µÄºÏ³É·½·¨£¬ÒÑÌá¸ß(¡À)-DSS, (¡À)-IDHP, and (¡À)-DBZµÄÉú²úÂÊ£¬Í¬Ê±£¬ÎªÂÌÉ«ºÏ³É¹ý³ÌѰÕÒ¶¾ÐÔ¸üСµÄ´ß»¯¼Á¡£¶øÇÒ£¬ÎÒÃÇҲΪ(¡À)-IDHP ºÍ (¡À)-DBZµÄÊÖÐÔ²ð·Ö¿ª·¢ÁËÒ»ÖÖ·½·¨£¬´Ó¶øµÃµ½¹âѧ´¿¶ÈµÄ R-IDHP, S-IDHP, R-DBZ, ºÍ S-DBZµÄͬ·ÖÒì¹¹Ìå¡£
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