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https://doi.org/10.1039/b712591g
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Cite Journal: Chem. Commun. |  Publication Date: Jan 1, 2008 |
 Citations: 68 |
Affiliation: Peking University
Under pre-activation glycosylation conditions, the 4,6-di-O-acetyl-N-acetyloxazolidinone protected donor afforded either excellent beta- or alpha-stereoselectivity simply by means of the addition of hindered base TTBP or the absence of base, leading to the controllable stereochemistry of coupling reactions.
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