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Direct Trifluoromethylthiolation Reactions: The “Renaissance” of an Old Concept

European Journal of Organic Chemistry · 2014 · Vol. 2014(12) · pp. 2415–2428
Fabien ToulgoatSébastien AlazetThierry Billard

Abstract

Abstract Because of its high lipophilicity, the CF 3 S group has always interested chemists. However, strategies to introduce it into organic molecules have been, for the most part, reserved to specialized “fluorine chemists”. Recent published work has demystified these preconceived ideas by proposing new efficient methods or easy‐to‐handle reagents to enrich the toolbox of chemists. However, all these new concepts arise from the pioneering works of the past! In this review, we will do a “back to the future” by remembering the most significant results of the past and by presenting extensions and novelties of the present and for the future.

Fluorine in Organic ChemistrySulfur-Based Synthesis TechniquesChemical Synthesis and AnalysisThe RenaissanceToolboxChemistryLipophilicityWork (physics)Management scienceEpistemologyComputer scienceOrganic chemistryEngineering

Funding

  • Centre National de la Recherche Scientifique
Citations
401
FWCI
29.07
field-weighted impact
References
136
Percentile
100%
vs. same field & year
Citations per year
Cited by
Late stage trifluoromethylthiolation strategies for organic compounds
Organic & Biomolecular Chemistry · 2016 · 285 citations
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