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- W2950481503 abstract "Synthesis of Segment C of tautomycin was accomplished from 2 D-sugar derivatives. New heteroconjugate addition strategy allowed stereocontrolled syntheses of the 2 sub-segments, C-1 and C-2, and 3 other diastereoisomers of the latter. Sub-segments were coupled between sulfone carbanion and epoxide electrophile to furnish the spiro ring moiety of the target compound." @default.
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- W2950481503 date "1995-03-01" @default.
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- W2950481503 title "Synthesis of Segment C of Tautomycin" @default.
- W2950481503 doi "https://doi.org/10.1055/s-1995-4937" @default.
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