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- W2949673591 abstract "Abstract Methyl 5- acetamido-7,8,9-tri -O- acetyl-4-azido-2,3-didehydro-2,3,4,5-tetradeoxy- d -glycero- d -talo- nonulopyranosonate with N-bromosuccinimide in methanol gave methyl (methyl 5- acetamido-7,8,9-tri -O- acetyl-4-azido-3-bromo-3,4,5-trideoxy-α- d -glycero- d -talo- nonulopyranosid)onate and methyl (methyl 5- acetamido-7,8,9-tri -O- acetyl-4-azido-3-bromo-3,4,5-trideoxy-β- d -glycero- d -talo- nonulopyranosid)onate , which on reductive acetylation with H 2 PdC in acetic anhydride-ethyl acetate yielded the corresponding 4-acetamido analogues. Debromination with Bu 3 SnH AIBN in toluene, followed by hydrolysis, gave methyl 4-acetamido-N-acetyl-4-deoxy-α-and β-4-epi-neuraminic acids." @default.
- W2949673591 created "2019-06-27" @default.
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- W2949673591 date "2010-08-12" @default.
- W2949673591 modified "2023-09-25" @default.
- W2949673591 title "ChemInform Abstract: Synthesis of Methyl 4-Acetamido-N-acetyl-4-deoxy-α- and β-4- epi-neuraminic Acids." @default.
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- W2949673591 doi "https://doi.org/10.1002/chin.199609246" @default.
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