Efficient synthesis of multifunctional furanoid C-glycoamino acid precursors
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文摘
Ready access to constrained, multifunctionalized, hydrolytically stable amino acids has been established by the synthesis of their direct precursors using 2,5-anhydro-3-azido-3-deoxy-d-altrose (a aaaformyl azido-C-glycofuranosideaaa), or its readily available, stable synthetic equivalent [(1R) and (1S)-2,5-anhydro-3-azido-4,6-O-benzylidene-3-deoxy-1-fluoro-1-O-methyl-d-altritol], as novel molecular scaffolds.

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