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Synthesis and Biological Activities of N-( 4-SubstItuted-phenyl) -N'- (1 '-beta- D-glucopyranosyl) - thiourea

机译:N-(4-取代 - 苯基)-N'-(1'β-D-吡喃葡萄糖基) - 硫脲的合成和生物活性

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Six N-(4-substituted-phenyl)-N'-( 2 , 3', 4', 6'-tetra~Oacetyl-beta-D-glucopyranosyl)-thioureas(4)were synthesized by condensation of 4-substituted-anilines(2)with 2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl isothiocyanate(3)in ethanol under reflux,respectively,and also six N-(4-substituted-phenyl]-N'-(l'-beta-D-glucopyranosyl)-thioureas(5)after deacetylation. Their structures were confirmed by IR,~1 H NMR, ESI-MS spectral data and elemental analyses. The biological activities of thecompounds were investigated.
机译:通过4-取代的缩合合成六种(2,3',4',(2,3',4',6'-四乙酰β-D-吡喃葡萄糖基)-Thioureas(4)。苯胺(2)分别在回流下的乙醇中具有2,3,4,6-四-4-乙酰β-β-D-吡喃葡萄糖(3),还有六个(4-取代 - 苯基] -N' - 脱乙酰化后(L'-Beta-D-吡喃葡萄糖基) - 硫脲(5)。通过IR,〜1 H NMR,ESI-MS光谱数据和元素分析证实了它们的结构。研究了Checonds的生物活性。

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