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An Approach to P = N Bond Formation: Straightforward Synthesis of Arylurea-Derived Phosphazenes via Condensation of Ph3P = O with N-Monosubstituted Arylureas

机译:P = N键形成的方法:通过N-单叠取代的芳脲的凝结通过PH3P = O的浓缩来直接合成芳基脲衍生的磷酸

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摘要

The Hendrickson's reagent-mediated formation of the P=N bond provides access to arylurea-derived phosphazenes compounds using readily available /V-monosubstituted arylureas and Ph3P=O. Various functional groups were tolerated to give arylurea-derived phosphazenes in the yield of 71-93%. The reaction also provides an alternative strategy for constructing compounds containing P=N bond. In this transformation, the Hendrickson's reagent unprecedented selectively reacts with the free amine group instead of the oxygen atom of N-monosubstituted arylurea. In addition, we found that thioureas could act as an effective thionating agent by converting Ph3P= O to Ph3P=S.
机译:亨德里克森(Hendrickson)的p = n键的试剂介导的形成提供了使用易于可用的 /v单溶剂构成的芳脲和pH3p = o的芳基脲衍生的磷酸化合物的访问。 可耐受各种官能团的产量为71-93%。 该反应还提供了构建包含p = n键的化合物的替代策略。 在这种转化中,亨德里克森的试剂前所未有地与自由胺基团反应,而不是n-单叠取代的芳基脲的氧原子。 此外,我们发现Thioureas可以通过将PH3P = O转换为PH3P = S来充当有效的毒剂。

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