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首页> 外文期刊>The Journal of Organic Chemistry >Facile Entry into Triazole Fused Heterocycles viaSuffamidate Derived Azido-alkynes
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Facile Entry into Triazole Fused Heterocycles viaSuffamidate Derived Azido-alkynes

机译:通过氨基磺酸盐衍生的叠氮基炔烃轻松地进入三唑融合杂环

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摘要

Direct synthesis of condensed triazoles from diversesulfamidates by ring opening of sulfamidates with sodiumazide followed by one-pot propargylation and cycloadd-ition furnished title compounds. The methodology ingeneral has been demonstrated on diverse sulfamidatesderived from amino acids, amino acid derivatives, andcarbohydrates to obtain diverse triazole fused scaffolds.In one example, a condensed triazole containing aminoacid has been synthesized by ring opening of a sulfarni-date derivative with propargyl amine.
机译:通过用叠氮化钠将氨基磺酸盐开环,然后一锅炔丙基化和环加成标题化合物,可以从多种氨基磺酸盐直接合成缩合三唑。通用的方法论已被证明可用于衍生自氨基酸,氨基酸衍生物和碳水化合物的多种氨基磺酸盐,以获得多种三唑稠合的支架。在一个实例中,通过将磺胺日期衍生物与炔丙基胺开环合成了含氨基酸的稠合三唑。

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