The stereoselective synthesis of the C6-C18 fragment of scytophycin C employing a novel synthetic methodology.

[摘要]：A novel synthetic approach towards the stereoselective synthesis of the C(6)-C(18) fragment (I) of the antitumor agent scytophycin C is described. The synthesis involves Marouka allylation, base-catalyzed intramol. conjugate addn., Wittig olefination, and a tandem allylation.

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