Abstract
Methyl 3,3-(ethylenedioxy)-6β-fluoro-5β-cholan-24-oate has been prepared starting from hyodeoxycholic acid and 3,3-(ethylenedioxy)-7(α and β)-fluorocholestan-22-al starting from stigmasterol, using diethylaminosulfur trifluoride as the fluorinating agent. These molecules will be used to synthesize analogs of the aminosterol antibiotic squalamine.
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