five

A Formal Synthesis of (-)-Cephalotaxine

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https://figshare.com/articles/dataset/A_Formal_Synthesis_of_Cephalotaxine/2927236
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An enantioselective formal synthesis of the alkaloid (−)-cephalotaxine has been completed, using an alkylidene carbene 1,5-CH insertion reaction as a key step to construct the spiro[4.4]azanonane core D/E-ring system. A Heck-type cyclization was used to close the tetrahydroazepine C-ring and a selective epoxidation−rearrangement sequence was used to elaborate the E-ring.
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2016-02-27
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