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- W2950164552 abstract "The extensive ring-expansion strategy for the synthesis of oxepene 19, oxocane 23, and oxonene 28, which correspond to the D (E), I and F ring fragments of ciguatoxin (1), respectively, has been established. Chemoenzymatic asymmetric acylation of the meso alcohols using lipase AK provided a simple entry of the enantiomeric building blocks." @default.
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- W2950164552 date "2010-08-04" @default.
- W2950164552 modified "2023-09-25" @default.
- W2950164552 title "ChemInform Abstract: Extensive Ring-Expansion Strategy for the Enantioselective Synthesis of the Medium Ring Ethers, Oxepene, Oxocane, and Oxonene, of Ciguatoxin." @default.
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- W2950164552 doi "https://doi.org/10.1002/chin.199721252" @default.
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