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- W2952575402 abstract "Catalytic and chemoselective glycosylation between novel “armed” and “disarmed” glycosyl p-trifluoromethylbenzylthio-p-trifluoromethylphenyl formimidates was effectively performed in the presence of a catalytic amount of TfOH and MS 4A in CH2Cl2 at -78 °C. In addition, it was noted that highly 1,2-cis or 1,2-trans stereoselective synthesis was established when the above glycosylation was carried out at -78 °C in tBuOMe or EtCN, respectively." @default.
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- W2952575402 date "2002-07-01" @default.
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- W2952575402 title "Catalytic and Chemoselective Glycosylation between “Armed” and “Disarmed” Glycosyl<i>p</i>-Trifluoromethylbenzylthio-<i>p</i>-trifluoromethylphenyl Formimidates" @default.
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- W2952575402 doi "https://doi.org/10.1246/cl.2002.746" @default.
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