Iron(II)-Catalyzed\nSynthesis of Nitrated Dihydropyrazole\nvia a Nitrification and C–H Activation/Cyclization Cascade\nReaction

A route for nitrification and C–H activation/cyclization\nof (<i>E</i>)-<i>N</i>-allyl-<i>N</i>′-benzylidenebenzenesulfonohydrazide and cobalt nitrate via\nan iron(II)-catalyzed cascade reaction to synthesize nitrated dihydropyrazoles\nhas been developed. The method features convenient operation and good\nfunctional group tolerance. In addition, it employs insensitive and\ninexpensive FeSO<sub>4</sub> as the catalyst and provides a direct\napproach for the preparation of dihydropyrazoles.

Publication Details

Journal
Figshare
Published
2024-11-07
DOI
https://doi.org/10.1021/acs.joc.4c00313.s001
Primary Topic
German History and Society
Type
article
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article

Iron(II)-Catalyzed\nSynthesis of Nitrated Dihydropyrazole\nvia a Nitrification and C–H Activation/Cyclization Cascade\nReaction

Figshare
German History and Society
article

Iron(II)-Catalyzed\nSynthesis of Nitrated Dihydropyrazole\nvia a Nitrification and C–H Activation/Cyclization Cascade\nReaction

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Abstract

A route for nitrification and C–H activation/cyclization\nof (<i>E</i>)-<i>N</i>-allyl-<i>N</i>′-benzylidenebenzenesulfonohydrazide and cobalt nitrate via\nan iron(II)-catalyzed cascade reaction to synthesize nitrated dihydropyrazoles\nhas been developed. The method features convenient operation and good\nfunctional group tolerance. In addition, it employs insensitive and\ninexpensive FeSO<sub>4</sub> as the catalyst and provides a direct\napproach for the preparation of dihydropyrazoles.

Figshare
Clean water and sanitation
Openalex Percentile: Top 46%
German History and Society
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Iron(II)-Catalyzed\nSynthesis of Nitrated Dihydropyrazole\nvia a Nitrification and C–H Activation/Cyclization Cascade\nReaction · Figshare (2024) | TGRS Research Map | TGRS