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Stereoselective organocatalyzed glycosylations – thiouracil thioureas and monothiophthalimide act as Brønsted acid catalysts at low loadings

机译:立体选择性有机催化的糖基化反应–硫尿嘧啶硫脲和单硫邻苯二甲酰亚胺在低负荷下充当布朗斯台德酸催化剂

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摘要

Thiouracil catalyzes stereoselective glycosylations with galactals in loadings as low as 0.1 mol%. It is proposed that in these glycosylations thiouracil, monothiophthalimide, and the previously reported catalyst, Schreiner's thiourea, do not operate via a double H-bonding mechanism but rather by Brønsted acid/base catalysis. In addition to the synthesis of 2-deoxyglycosides and glycoconjugates, we report the first organocatalytic synthesis of 1,1′-linked trehalose-type sugars.
机译:硫脲嘧啶以低至0.1 mol%的负载量催化半乳糖的立体选择性糖基化反应。建议在这些糖基化反应中,硫氧尿嘧啶,单硫代邻苯二甲酰亚胺和先前报道的催化剂Schreiner的硫脲不通过双重H键机理而是通过布朗斯台德酸/碱催化作用。除了2-脱氧糖苷和糖缀合物的合成,我们还报道了1,1'-连接的海藻糖型糖的首次有机催化合成。

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