A chemoenzymatic and enantioselective total synthesis of the resorcylic acid lactone L-783,290, the trans -isomer of L-783,277
The structure, 5, assigned to the resorcylic acid lactone L-783,290 has been prepared for the first time and in a modular fashion using a Heck reaction to link the readily available fragments 8 and 14. Chemoenzymatic methods were used to prepare the latter fragment, in enantiopure form, from chlorobenzene.
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