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首页> 外文期刊>Canadian Journal of Chemistry >Hetero-Diels-Alder reactions involving Fe(CO)3-coordinated dienal and formyltrimethylenemethane catalyzed by Lewis acids - A theoretical study
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Hetero-Diels-Alder reactions involving Fe(CO)3-coordinated dienal and formyltrimethylenemethane catalyzed by Lewis acids - A theoretical study

机译:路易斯酸催化的Fe(CO)3配位二烯和甲酰三亚甲基甲烷的杂Diels-Alder反应-理论研究

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摘要

The hetero-Diels-Alder reactions of butadiene with Fe(CO)3-coordinated formylbutadiene and formyltrimethyle-nemethane catalyzed by Lewis acids have been theoretically studied through density functional calculations. The results obtained show that, for the reaction with (formylbutadiene)Fe(CO)3, the kinetically most favourable product is the one corresponding to the attack of butadiene on the s-cis conformer of the formylbutadiene fragment when the reaction is catalyzed by BF3, and the one corresponding to the attack on the s-trans conformer when the catalyst is TiCl4. On the other hand, for the reaction with (formyltrimethylenemethane)Fe(CO)3 catalyzed by BF3, the product corresponding to the attack on the s-trans conformer is predicted to be favoured. These results have been interpreted through an energy decomposition analysis of the potential-energy barriers.
机译:通过密度泛函计算,从理论上研究了丁二烯与Fe(CO)3-配位的甲酰基丁二烯和路易斯三酸催化的甲酰基三甲基-neane甲烷的杂Diels-Alder反应。所得结果表明,对于与(甲酰基丁二烯)Fe(CO)3的反应,动力学上最有利的产物是当BF 3催化反应时,对应于丁二烯对甲酰基丁二烯片段的s-顺式构象的攻击的产物。 ,和对应于当催化剂为TiCl4时对s-反式构象异构体的攻击。另一方面,对于与被BF 3催化的(甲酰基三亚甲基甲烷)Fe(CO)3的反应,预计对与反式构象异构体的进攻相对应的产物是有利的。通过对势能垒的能量分解分析来解释这些结果。

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