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Iron(II) catalyzed reductive radical cyclization reactions of bromoacetals in the presence of NaBH4: optimization studies and mechanistic insights

机译:NaBH4存在下铁(II)催化溴缩醛的还原自由基环化反应:优化研究和机理研究

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摘要

5-Exo-trig radical reductive cyclization reactions of bromoacetals are catalyzed by iron in the presence of the reducing agent NaBH4. Both iron(II) and iron(III) were found to effectively mediate these reactions. As shown by cyclic voltammetry, iron(III) can be reduced to an iron(II) precatalyst before passing through an identical reaction mechanism in which monoelectronic activation of the substrate would occur by an anionic hydridoiron(I) complex. Further studies have established that both the substrate (iodo- vs bromo-derivative) and the precatalytic mixture are decisive in determining the reaction outcome. (C) 2016 Elsevier Ltd. All rights reserved.
机译:在还原剂NaBH4存在下,铁催化溴乙缩醛的5-Exo-trig自由基还原环化反应。发现铁(II)和铁(III)均可有效介导这些反应。如循环伏安法所示,在通过相同的反应机理之前,铁(III)可以还原为铁(II)预催化剂,在该反应机理中,阴离子氢化铁(I)络合物会发生底物的单电子活化。进一步的研究已经确定,底物(碘衍生物与溴衍生物)和预催化混合物均对确定反应结果具有决定性作用。 (C)2016 Elsevier Ltd.保留所有权利。

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