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- W2036735568 abstract "A stereocontrolled synthesis of two diastereomeric C1-C22 fragments of spirastrellolide A consistent with reported spectroscopic data has been achieved to aid in a complete configurational assignment of this structurally novel and potent antimitotic natural product. A highly convergent coupling of two enantiomeric C1-C10 methyl ketone fragments with an enantiopure C11-C22 spiroketal aldehyde produced the C1-C22 fragments with a longest linear sequence of 13 steps from commercially available starting materials." @default.
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- W2036735568 date "2006-03-14" @default.
- W2036735568 modified "2023-10-01" @default.
- W2036735568 title "Synthesis of Spirastrellolide A Fragments for Structure Elucidation" @default.
- W2036735568 doi "https://doi.org/10.1055/s-2006-933144" @default.
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