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• W2040666564 startingPage "1044" @default.
• W2040666564 abstract "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." @default.
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• W2040666564 date "2010-02-01" @default.
• W2040666564 modified "2023-10-16" @default.
• W2040666564 title "A chemoenzymatic and enantioselective total synthesis of the resorcylic acid lactone L-783,290, the trans-isomer of L-783,277" @default.
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• W2040666564 doi "https://doi.org/10.1016/j.tetlet.2009.12.067" @default.
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