期刊
JOURNAL OF PHYSICAL ORGANIC CHEMISTRY
卷 32, 期 12, 页码 -出版社
WILEY
DOI: 10.1002/poc.4011
关键词
captodative olefins; DFT; Friedel-Crafts; IRC; Parr functions
资金
- Universidad Michoacana de San Nicolas de Hidalgo
- Consejo Nacional de Ciencia y Tecnologia [252239]
- Secretaria de Educacion Publica [PFCE-2017-10]
The regioselectivity of the conjugate addition between syringol (1) and the captodative olefin 3-(p-nitrobenzoyloxy)-but-3-en-2-one (2) is evaluated under diverse solvent and Lewis acid catalyst conditions, providing a mixture of the para/meta phenol adducts. Experimental results revealed for most of the trials that the para regioisomer is the major one. However, there is not a clear correlation between the regioselectivity of products and the polarity of the tested solvents. In this work, the reactivity descriptors and the reaction mechanism are studied in the framework of the density functional theory (DFT) to give insights about the reactivity and regioselectivity of this reaction. The Parr functions difference is used as the reactivity descriptor in each stage of the reaction explaining quite well the involved transition states. Overall, it is found that the reactivity of 1 is strongly influenced by the presence of the catalyst, while the regioselectivity of the products depends on both the catalyst and the polarity of the solvent, finding that, the meta adduct is highly dependent of the presence of nonpolar solvents.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据