1. Combined inorganic base promoted N-addition/[2,3]-sigmatropic rearrangement to construct homoallyl sulfur-containing pyrazolones
- Author
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Xiao-Li Du, Jin-Yan Liang, Xiao-Li Xu, Ming-gang Zhao, Yue-Hua Wu, and Shou-Jie Shen
- Subjects
chemistry.chemical_classification ,Annulation ,Base (chemistry) ,Sulfonium ,General Chemical Engineering ,2,3-sigmatropic rearrangement ,Regioselectivity ,02 engineering and technology ,General Chemistry ,010402 general chemistry ,021001 nanoscience & nanotechnology ,01 natural sciences ,Medicinal chemistry ,0104 chemical sciences ,chemistry.chemical_compound ,chemistry ,Propargyl ,Pyrazolones ,Rearrangement reaction ,0210 nano-technology - Abstract
The first sequentially combined inorganic base promoted N-addition/[2,3]-sigmatropic rearrangement reaction of α-alkylidene pyrazolinones and propargyl sulfonium salts has been reported to construct homoallyl sulfur-containing pyrazolones with moderate to excellent yields. α-Alkylidene pyrazolinones function as N-nucleophilic agents distinguished from the reported C-addition reactions. Propargyl sulfonium salts were first involved in the [2,3]-sigmatropic rearrangement protocol differentiated from the well-established annulation reactions. The excellent regioselectivity, the broad scope of substrates, gram-scale synthesis and convenient transformation embody the synthetic superiority of this cascade process.
- Published
- 2019
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