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α-亚烷基吡唑啉酮与炔丙基锍盐的区域选择性N-加成/取代反应构建含烯丙硫基的吡唑啉酮

Regioselective N-Addition/Substitution Reaction of α-Alkylidene Pyrazolinones with Propargyl Sulfonium Salts to Construct Allylthio-Containing Pyrazolones.

作者信息

Shen Shou-Jie, Du Xiao-Li, Xu Xiao-Li, Zhao Ming-Gang, Liang Jin-Yan

出版信息

J Org Chem. 2019 Oct 4;84(19):12520-12531. doi: 10.1021/acs.joc.9b02029. Epub 2019 Sep 20.

Abstract

The regioselective N-addition/substitution reaction between α-alkylidene pyrazolinones and propargyl sulfonium salts has been developed to construct functionalized allylthio-containing pyrazolones with moderate to excellent yields. α-Alkylidene pyrazolinones act as N-nucleophilic agents which are distinguished from reported C-nucleophilic reactions. Excellent regioselectivity, readily available starting materials, the broad range of substrates, gram-scale synthesis, and simple operation illustrate the synthetic advantages of this new reaction pathway.

摘要

已开发出α-亚烷基吡唑啉酮与炔丙基锍盐之间的区域选择性N-加成/取代反应,以中等至优异的产率构建功能化的含烯丙硫基吡唑啉酮。α-亚烷基吡唑啉酮作为N-亲核试剂,这与已报道的C-亲核反应不同。优异的区域选择性、易于获得的起始原料、广泛的底物范围、克级规模的合成以及操作简单,说明了这种新反应途径的合成优势。

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