Abstract
The first stereo selective synthesis of 5-O-feruloyl-2-deoxy-d-ribono-γ-lactone was achieved by coupling reaction of substituted ferulic acid and hydroxy methyl ribono lactone and followed by deprotection of O-PMB. The spectroscopic data were compared with the reported values and a clear indication to the absolute stereochemistry of the natural 5-O-feruloyl-2-deoxy-d-ribono-γ-lactone.
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