Mechanistic Insights into the Pd-Catalyzed Intermolecular Asymmetric Allylic Dearomatization of Multisubstituted Pyrroles: Understanding the Remarkable Regio- and Enantioselectivity
Zheng C(郑超); Zhuo CX(卓春祥); You SL(游书力)
刊名J. Am. Chem. Soc.
2014
卷号136期号:46页码:16251-16259
其他题名钯催化多取代吡咯的分子间不对称烯丙基去芳构化的机理考察: 理解反应优异的区域选择性与对映选择性
通讯作者郑超 ; 游书力
英文摘要In this article we report a comprehensive density functional theory study on the Pd-catalyzed intermolecular asymmetric allylic dearomatization reactions of multisubstituted pyrroles. The calculated results are in line with the previous experimental observations (J. Am. Chem. Soc. 2014, 136, 6590), and the remarkable regio- and enantioselectivity are well explained. Of all the potential nudeophilic sites around the multisubstituted pyrrole ring, the reaction always occurs at the position where the HOMO of the molecule distributes most significantly. In contrast to the common view on the enantioselectivity of the Pd-catalyzed asymmetric allylic substitution reactions, we find that the steric interaction between the nucleophile and the chiral ligand does not have the dominating effect on the enantioselectivity of the reaction. Instead, the interaction between the allyl moiety and the incoming nucleophile plays an important role in the enantioselectivity-determining process.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1021/ja5080135
语种英语
内容类型期刊论文
源URL[http://ir.sioc.ac.cn/handle/331003/39130]  
专题上海有机化学研究所_金属有机化学国家重点实验室
作者单位中科院上海有机化学研究所
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Zheng C,Zhuo CX,You SL. Mechanistic Insights into the Pd-Catalyzed Intermolecular Asymmetric Allylic Dearomatization of Multisubstituted Pyrroles: Understanding the Remarkable Regio- and Enantioselectivity[J]. J. Am. Chem. Soc.,2014,136(46):16251-16259.
APA 郑超,卓春祥,&游书力.(2014).Mechanistic Insights into the Pd-Catalyzed Intermolecular Asymmetric Allylic Dearomatization of Multisubstituted Pyrroles: Understanding the Remarkable Regio- and Enantioselectivity.J. Am. Chem. Soc.,136(46),16251-16259.
MLA 郑超,et al."Mechanistic Insights into the Pd-Catalyzed Intermolecular Asymmetric Allylic Dearomatization of Multisubstituted Pyrroles: Understanding the Remarkable Regio- and Enantioselectivity".J. Am. Chem. Soc. 136.46(2014):16251-16259.
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