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Formal Total Synthesis of (–)-Raphidecursinol B

✍ Scribed by Sanjit Kumar Das; Sajal Kumar Das; Gautam Panda


Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
245 KB
Volume
2010
Category
Article
ISSN
1434-193X

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✦ Synopsis


Abstract

An efficient enantioselective formal total synthesis of antimalarial natural product (–)‐raphidecursinol B along with its all stereoisomers is described from commercially available 3,4,5‐trimethoxybenzaldehyde using the Sharpless asymmetric dihydroxylation, regioselective α‐tosylation, epoxide opening and Mitsunobu reaction as the key reaction steps.


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