An Efficient Stereoselective Approach for the Synthesis of (+)-( 4S,5S)-Muricatacin

[摘要]：An efficient stereoselective total synthesis of (+)-(4S,5S)-muricatacin was accomplished in good yields from inexpensive, commercially available chemicals ((+)-diethyl tartrate (DET) and undecan-1-ol) by utilizing Mitsunobu and Julia-Kocienski reactions, Wittig homologation, Swern oxidation, and lactonization.

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