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Yongan Liu

Researcher at Chinese Academy of Sciences

Publications -  10
Citations -  250

Yongan Liu is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Trifluoromethyl & Sulfonyl. The author has an hindex of 6, co-authored 10 publications receiving 141 citations.

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Arenesulfonyl Fluoride Synthesis via Copper-Catalyzed Fluorosulfonylation of Arenediazonium Salts.

TL;DR: A general and practical copper-catalyzed fluorosulfonylation reaction of a wide range of abundant arenediazonium salts to smoothly prepare various arenesulfonyl fluorides using the 1,4-diazabicyclo(sulfur dioxide) adduct as a convenient sulfonyl source in combination with KHF2 as an ideal fluorine source and without the need for additional oxidants.
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Trifluoromethylfluorosulfonylation of Unactivated Alkenes Using Readily Available Ag(O2CCF2SO2F) and N‐fluorobenzenesulfonimide

TL;DR: A novel intermolecular radical trifluoromethyl and sulfonyl groups in the products originate from Ag(O2 CCF2 SO2 F) and N-fluorobenzenesulfonimide (NFSI).
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Intermolecular oxidative radical fluoroalkylfluorosulfonylation of unactivated alkenes with (fluoroalkyl)trimethylsilane, silver fluoride, sulfur dioxide and N-fluorobenzenesulfonimide

TL;DR: An intermolecular oxidative radical fluoroalkylfluorosulfonylation reaction of unactivated alkenes with convenient and commercially available (fluoroalkyl)trimethylsilane, silver fluoride, sulfur dioxide and N-fluorobenzenesulfonimide (NFSI) is described in this article.
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Zinc‐Mediated Intermolecular Reductive Radical Fluoroalkylsulfination of Unsaturated Carbon–Carbon Bonds with Fluoroalkyl Bromides and Sulfur Dioxide

TL;DR: A versatile and general zinc-mediated intermolecular reductive radical fluoroalkylsulfination of unsaturated C-C bonds has been developed using readily available fluoroalksyl bromides and 1,4-diazabicyclo[ 2.2.2]octane-bis(sulfur dioxide) adduct with wide substrate scope and excellent functional group tolerance.
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Oxidative Radical Intermolecular Trifluoromethylthioarylation of Styrenes by Arenediazonium Salts and Copper(I) Trifluoromethylthiolate

TL;DR: An efficient oxidative radical intermolecular trifluoromethylthioarylation of styrenes with arenediazonium salts and copper(I) trifLUorometHylthiolate under mild conditions is described for the first time.