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Synthesis and reactivity of novel sulfur pentafluorides-Effect of the SF5 group on reactivity of nitrobenzenes in nucleophilic substitution

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    0474386 - ÚOCHB 2018 RIV GB eng J - Journal Article
    Beier, Petr
    Synthesis and reactivity of novel sulfur pentafluorides-Effect of the SF5 group on reactivity of nitrobenzenes in nucleophilic substitution.
    Phosphorus, Sulfur and Silicon and the Related Elements. Roč. 192, č. 2 (2017), s. 212-215. ISSN 1042-6507. E-ISSN 1563-5325.
    [International Symposium on the Organic Chemistry of Sulfur (ISOCS) /27./. Jena, 26.07.2016-29.07.2016]
    Institutional support: RVO:61388963
    Keywords : nucleophilic substitution * sulfur * fluorine * reaction rate
    OECD category: Organic chemistry
    Impact factor: 0.674, year: 2017

    The latest achievements in the synthesis of aromatic and heteroaromatic pentafluorosulfanyl-substituted compounds by nucleophilic substitution approach are summarized. The effect of the SF5 group on relative reactivities in a model vicarious nucleophilic substitution (VNS) is, reported. The pentafluorosulfanyl group was found to activate nitrobenzenes for VNS more strongly than trifluoromethyl or cyano groups.
    Permanent Link: http://hdl.handle.net/11104/0271448

     
     
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