Publication | Closed Access
Synthesis of Natural Ecteinascidins (ET-729, ET-745, ET-759B, ET-736, ET-637, ET-594) from Cyanosafracin B
75
Citations
46
References
2003
Year
Selective OxidationOther Natural EcteinascidinsBiosynthesisBioorganic ChemistryBiochemistryCyanosafracin BNatural EcteinascidinsNatural SciencesMedicineMolecular BiologyOrganic ChemistrySynthetic ChemistryPharmacologyPharmaceutical ChemistrySemisynthetic ProcessEnantioselective SynthesisDrug DiscoveryNatural Product Synthesis
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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