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Synthesis and characterization of N-glucosylated dithiadiazepine derivatives through carbon-sulfur bond formation

机译:通过碳-硫键的形成合成和表征N-葡萄糖基化的二硫杂二氮杂卓

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摘要

New 4,7-bis(arylamino)-2-tetra-O-acetyl-beta-D-glucopyranosylimino-1,3,5,6-dithiadiazepines were synthesized via reaction of N-tetra-O-acetyl-beta-D-glucopyranosyl isocyanodichloride with 1,6-diaryl-2,5-dithio-bis-ureas without using any catalyst. Thus, the synthesis of 7-membered heterocycles containing two sulfur and two nitrogen atoms through carbon-sulfur bond formation was explored. The chemical structures of these new compounds were elucidated by IR, H-1 NMR, C-13 NMR, mass spectral, and elemental analyses.
机译:通过N-四-O-乙酰基-β-D-的反应合成了新的4,7-双(芳基氨基)-2-四-O-乙酰基-β-D-吡喃葡萄糖基-1,3,5,6-二硫二氮杂ze。吡喃葡萄糖基异氰基二氯化物与1,6-二芳基-2,5-二硫代-双-脲的合成,无需使用任何催化剂。因此,探索了通过碳-硫键的形成合成包含两个硫和两个氮原子的7元杂环。通过IR,H-1 NMR,C-13 NMR,质谱和元素分析阐明了这些新化合物的化学结构。

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