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- W2169487263 abstract "An efficient method for the stereoselective synthesis of 2-amino-2-deoxy-d-arabinose and 2-deoxy-d-ribose is described.The key step in this method was accomplished by the nucleophilic addition of methyl isocyanoacetate to 2,3-O-isopropylidene-d-glyceraldehyde with high erythro-selectivity (nearly 100%).Subsequent intermolecular cyclization predominantly gave the desired oxazoline derivative (trans-form), in which two new chiral centers were formed. The oxazoline derivative was efficiently converted to both 2-amino-2-deoxy-d-arabinose and 2-deoxy-d-ribose." @default.
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- W2169487263 date "1985-01-01" @default.
- W2169487263 modified "2023-10-17" @default.
- W2169487263 title "Stereoselective synthesis of 2-amino-2-deoxy-D-arabinose and 2-deoxy-D-ribose." @default.
- W2169487263 doi "https://doi.org/10.1271/bbb1961.49.1435" @default.
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