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- W2005498047 abstract "The synthesis of fused furanosyl β-amino esters from protected sugar lactones is described, using the combination of a Wittig type reaction and 1,4-addition of benzylamine on the resulting glycosylidenes. This sequence of reactions afford either N-glycosyl-3-ulosonic acid esters, which are the β-analogues of anomeric sugar α-amino esters, or open-chain sugar β-enamino esters, when a retro-Michael reaction takes place after addition of benzylamine. Incorporation of the fused furanosyl β-amino ester 2a into a peptide chain is also described." @default.
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- W2005498047 date "2002-08-01" @default.
- W2005498047 modified "2023-10-03" @default.
- W2005498047 title "Facile synthesis of fused furanosyl β-amino acids from protected sugar lactones: incorporation into a peptide chain" @default.
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- W2005498047 doi "https://doi.org/10.1016/s0957-4166(02)00473-1" @default.
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