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首页> 外文期刊>Chemical science >Dinuclear manganese alkoxide complexes as catalysts for C–N bond cleavage of simple tertiary N,N-dialkylamides to give esters
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Dinuclear manganese alkoxide complexes as catalysts for C–N bond cleavage of simple tertiary N,N-dialkylamides to give esters

机译:二核锰醇盐配合物作为简单叔N,N-二烷基酰胺的C-N键切割的催化剂给予酯

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Amide bonds are stable due to the resonance between the nitrogen lone pair and the carbonyl moiety, and therefore the chemical transformation of amides, especially tertiary amides, involving C–N bond fission is considered one of the most difficult organic reactions, unavoidably requiring harsh reaction conditions and strong acids or bases. We report the catalytic C–N bond cleavage of simple tertiary N , N -dialkylamides to give corresponding esters using a catalyst system (2 mol% based on Mn atoms) of a tetranuclear manganese alkoxide, [Mn(acac)(OEt)(EtOH)] _(4) ( 1c ), combined with four equivalents of 4,7-bis(dimethylamino)-1,10-phenanthroline ( L1 : Me _(2) N-Phen). Regarding the reaction mechanism, we isolated a dinuclear manganese complex, [Mn(acac)(OEt)(Phen)] _(2) ( 6c ), which was revealed as the catalytically active species for the esterification of tertiary amides.
机译:由于氮气缸对和羰基部分之间的共振,因此酰胺键是稳定的,因此酰胺的化学转化,尤其是叔酰胺,涉及C-N键裂变的化学转化被认为是最困难的有机反应之一,不可避免地需要恶劣的反应条件和强酸或碱。我们报告了简单叔镍N,N-二硫酰胺的催化C-N键切割,得到了四核锰醇醇盐的催化剂体系(2mol%)的相应酯[Mn(Acac)(OET)(EtOH )] _(4)(1c),与4当量的4,7-双(二甲基氨基)-1,10-菲咯啉(L1:Me _(2)n-pen)组合。关于反应机制,我们分离了核锰络合物,[Mn(Acac)(OET)(Ph)] _(2)(6C),其被揭示为催化活性物质,用于施用叔酰胺。

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