Abstract
Abstract Alkyl di-(9-fluorenylmethyl) phosphates obtained via phosphitylation were found to be suitable for protection of phosphoric monoesters, which were generated by treatment of the triesters with DBU or triethylamine. This strategy and a hydroxyl protecting group, 2-[2-(levulinoyloxy)ethyl]benzoyl were applied to synthesis of a dioleoyl analog of PI(4,5)P 2 .
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