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      Synthesis of natural ecteinascidins (ET-729, ET-745, ET-759B, ET-736, ET-637, ET-594) from cyanosafracin B.

      The Journal of Organic Chemistry
      Azocines, chemistry, Isoquinolines, chemical synthesis, Magnetic Resonance Spectroscopy, Mass Spectrometry, Quinones, Spectrophotometry, Infrared, Spectrum Analysis

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          Abstract

          The semisynthetic process initially described for the synthesis of 1 (ET-743) has been extended to the preparation of other natural ecteinascidins. For the synthesis of 2 (ET-729) a demethylation of a N-Me intermediate was carried out by a selective oxidation with MCPBA. Other natural ecteinascidins (ET-745, ET-759B, ET-736, ET-637, ET-594) were accessible from key intermediate 25. The described methodologies allow for the preparation of a wide variety of ecteinascidins by procedures that can be easily scaled up.

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