Fe-Catalyzed tandem cyclization for the synthesis of 3-nitrofurans from homopropargylic alcohols and Al(NO3)3·9H2O

Literature Information

Publication Date 2018-07-02
DOI 10.1039/C8OB01184B
Impact Factor 3.876
Authors

Ting Wang, Yong Jiang, Yanyan Wang, Rulong Yan


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Abstract

Al(NO3)3路9H2O as a nitro source for the synthesis of 3-nitrofurans from homopropargylic alcohols through Fe-catalyzed tandem cyclization is described. In this transformation, the substituted nitrofurans are obtained through nitration and cyclization. The substrate homopropargylic alcohols with different groups participate smoothly in this process and the desired substituted nitrofurans were obtained in moderate yields.

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Organic & Biomolecular Chemistry

Organic & Biomolecular Chemistry
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