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Stereoselective synthesis of the densely functionalized C1-C9 fragment of amphidinolides C and F
Authors:Debendra K Mohapatra  Pavankumar Dasari  Rita Pal
Institution:a Organic Chemistry Division-I, Indian Institute of Chemical Technology (CSIR), Hyderabad 500 007, India
b Organic Chemistry Division, National Chemical Laboratory (CSIR), Pune 411 008, India
Abstract:The synthesis of the C1-C9 subunit of amphidinolides C and F is described. Key steps include tandem Sharpless asymmetric dihydroxylation-SN2 cyclization reaction, Lewis acid-mediated epoxide opening, Wittig reaction, and Wacker oxidation.
Keywords:Amphidinolide C and F  Cytotoxic  Tandem dihydroxylation-SN2  Wittig reaction  Wacker oxidation
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