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• W2079657957 endingPage "10620" @default.
• W2079657957 startingPage "10603" @default.
• W2079657957 abstract "The “naked sugar” (+)-(1R, 4R)-7-oxabicyclo[2.2.1]hept-5-en-one((+)-2) has been converted to D-lividosamine ((+)-1: 3-deoxy-D-glucosamine) and derivatives via (+)-2-chloro-2,3-dideoxy-5,6-O-isopropylidene-D-arabino-hexono-1,4-lactone ((+)-33) and (+)-2-azido-2,3-dideoxy-5,6-O-isopropylidene-D-ribo-hexono-1,4-lactone ((+)-34) in a highly stereoselective fashion. Similarly, 2-acetamido-2,3-dideoxy-D-arabino-hexose and derivatives were derived from the “naked sugar” (−)-(1S,4S-7-oxabicyclo[2.2.1]-hept-5-en-2-one ((−)-2) via the double hydroxylation of the CC double bond in (−)-N-benzyl-N-[(1R,2S,4S)-6-bromo-7-oxabicyclo[2.2.1]hept-5-en-2-endo-yl] amine ((−)-40)." @default.
• W2079657957 created "2016-06-24" @default.
• W2079657957 creator A5059812669 @default.
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• W2079657957 creator A5040796329 @default.
• W2079657957 date "1992-11-01" @default.
• W2079657957 modified "2023-10-09" @default.
• W2079657957 title "Total asymmetric syntheses of d-lividosamine and 2-acetamido-2,3-dideoxy-d-arabino-hexose derivatives." @default.
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• W2079657957 doi "https://doi.org/10.1016/s0040-4020(01)88357-5" @default.
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