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- W2004356188 abstract "The synthesis of (+-)-4-epi-acetomycin has been completed by the steroselective ester enolate (Carroll rearrangement of (E)-2-butenyl 2-methylacetoacetate, followed by ozonolysis and acetylation. The synthesis of (±)- acetomycin and its three diastereomers by a related route is also described." @default.
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- W2004356188 date "2005-05-01" @default.
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- W2004356188 title "Generation of attenuation correction map for hybrid PET by automated image registration" @default.
- W2004356188 doi "https://doi.org/10.1016/j.ics.2005.03.159" @default.
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