首页> 外文期刊>Catalysis science & technology >DFT computational insight into Pd(0)-catalyzed oxidative cross-coupling of 1,2-allenyl ketones and aryl boronic acids: Pd(ii)-carbenoid intermediate versus π-allyl-Pd(ii) intermediate
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DFT computational insight into Pd(0)-catalyzed oxidative cross-coupling of 1,2-allenyl ketones and aryl boronic acids: Pd(ii)-carbenoid intermediate versus π-allyl-Pd(ii) intermediate

机译:DFT computational insight into Pd(0)-catalyzed oxidative cross-coupling of 1,2-allenyl ketones and aryl boronic acids: Pd(ii)-carbenoid intermediate versus π-allyl-Pd(ii) intermediate

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摘要

DFT calculations unveil that the Pd(0)-catalyzed oxidative cross-coupling of 1,2-allenyl ketones with aryl boronic acids may either occur via a Pd(ii)-carbenoid intermediate or a π-allyl-Pd(ii) intermediate, depending on the substituents on 1,2-allenyl ketones. The substituted substrate prefers to undergo the π-allyl-Pd(ii) intermediate mechanism over the Pd(ii)-carbenoid intermediate one, while the unsubstituted one reverses the preference. The calculations also show a new mechanism for the transformation of Pd(0) to the Pd(ii) complex and rationalize the reason for the non-excellent yield for the unsubstituted 1,2-allenyl ketone.
机译:DFT计算推出Pd(0)催化氧化交叉耦合的2-allenyl酮与芳基boronic酸可以通过一个发生钯(ii) -carbenoid中间或π-allyl-Pd (2)中间,这取决于取代基1, 2-allenyl酮。更愿意接受π-allyl-Pd (2)中间在Pd (2) -carbenoid机制中间的一个,而未被取代的逆转的偏好。显示一个新的机制的转变Pd (0) Pd (ii)复杂和合理化的客观性、产生的理由未被取代的1,2-allenyl酮。

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