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Two strategies demonstrate expedient and concise routes for the synthesis of heptamethyllithospermate from readily available starting materials. Moreover, these two strategies were applied successfully in a total synthesis of (+)-lithospermic acid with an anti-HIV activity.

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The firrst asymmetric syntheses of (+)-(R)-methyl lactate 3 (>99%ee) was completed in four steps with an overall yield of 75% from commercially available 3,4-dimethoxybenzaldehyde.

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This page is a summary of: Synthesis of anti-HIV lithospermic acid by two diverse strategies, Organic & Biomolecular Chemistry, January 2012, Royal Society of Chemistry,
DOI: 10.1039/c2ob25575h.
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