Synthetic Studies on Ecteinascidin 743

来源 :The 24th International Society of Heterocyclic Chemistry Con | 被引量 : 0次 | 上传用户:a67273271
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The key intermediate ofecteinascidin 743[1] was efficiently synthesized from sesamol in 11 steps and 25% overall yield.The key steps are a Noyori reduction, a diastereoselective Claisen rearrangement,[2] and cyclization of an acyliminium salt.
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