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Synthesis of the Death-Cap Mushroom Toxin α-Amanitin
Kaveh Matinkhoo1, Alla Pryyma1, Mihajlo Todorovic1
1Chemistry Department , The University of British Columbia , 2036 Main Mall , Vancouver , British Columbia V6T-1Z1 , Canada.
Abstract:
α-Amanitin is an extremely toxic bicyclic octapeptide isolated from the death-cap mushroom, Amanita phalloides. As a potent inhibitor of RNA polymerase II, α-amanitin is toxic to eukaryotic cells. Recent interest in α-amanitin arises from its promise as a payload for antibody-drug conjugates. For over 60 years, A. phalloides has been the only source of α-amanitin. Here we report a synthesis of α-amanitin, which surmounts the key challenges for installing the 6-hydroxy-tryptathionine sulfoxide bridge, enantioselective synthesis of (2 S,3 R,4 R)-4,5-dihydroxy-isoleucine, and diastereoselective sulfoxidation.
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