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The first synthesis of pyridinium N-benzoylguanidines by bismuth- and mercury-promoted guanylation of N-iminopyridinium ylide with thioureas

机译:铋和汞促进的N-亚氨基吡啶鎓内鎓盐与硫脲的胍基化反应首次合成吡啶鎓N-苯甲酰胍

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摘要

This work describes the first successful synthesis of five pyridinium N-benzoylguanidines. These new pyridinium ylides were prepared in moderate to good yields through the guanylation reaction of N-iminopyridinium ylide with N-benzoylthioureas, using both bismuth nitrate and mercury chloride as inorganic thiophiles. X-ray analysis of one pyridinium N-benzoylguanidine was investigated and the E configuration assigned. Intermolecular interactions of the type C-H center dot center dot center dot O and C-H center dot center dot center dot pi were observed in the solid state. The results related in this study represent the first description of a ylide as the nucleophilic partner in the guanylation reaction. (c) 2005 Elsevier Ltd. All rights reserved.
机译:这项工作描述了五个吡啶N-苯甲酰胍的首次成功合成。这些新的吡啶鎓叶立德是通过将硝酸亚氨基吡啶鎓叶立德与N-苯甲酰硫脲进行鸟嘌呤化反应,以硝酸铋和氯化汞为无机硫亲和剂,以中等至良好的产率制备的。研究了一种吡啶鎓N-苯甲酰胍的X射线分析,并确定了E构型。在固态下观察到C-H中心点中心点中心点O和C-H中心点中心点中心点pi的分子间相互作用。这项研究相关的结果代表了叶立德在鸟苷酸化反应中作为亲核伴侣的首次描述。 (c)2005 Elsevier Ltd.保留所有权利。

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