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March 3, 2026The Journal of Organic Chemistry4 citations

Photoinduced Tandem Cyclization of Unsaturated Hydrazones with CF 3 CH 2 I to Access Trifluoroethylated Tetrahydropyridazines and Dihydropyrazoles

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GYGuocheng YinChangzhou UniversityYCYangjian ChengMinjiang UniversitySYSheng YuChangzhou University

Key Points

  • Trifluoroethylated tetrahydropyridazines are synthesized using hydrazones and visible light.
  • The reaction achieved good functional group compatibility, indicating broad applicability in synthetic chemistry.
  • Observational analysis of trifluoroethylation and cyclization reactions with CF3CH2I was conducted under mild conditions.
  • These findings may enable the development of new trifluoroethylated compounds for pharmaceutical applications.

Abstract

A visible-light-mediated trifluoroethylation/cyclization reaction of N-homoallyl aldehyde hydrazones with 1,1,1-trifluoro-2-iodoethane (CF3CH2I) was developed for the synthesis of trifluoroethylated tetrahydropyridazines. The reaction was conducted under mild conditions with good functional group compatibility. Moreover, the synthesis of trifluoroethylated dihydropyrazoles was also achieved via the trifluoroethylation/cyclization of N-allyl aldehyde hydrazones with CF3CH2I.

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Cite This Study

Yin et al. (2026) studied this question.

synapsesocial.com/papers/69a75bcfc6e9836116a23ce0https://doi.org/10.1021/acs.joc.5c02897
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