Literature DB >> 28098311

Transition metal-free direct trifluoromethylthiolation of indoles using trifluoromethanesulfonyl chloride in the presence of triphenylphosphine.

Kui Lu1, Zhijie Deng2, Ming Li1, Tianjiao Li2, Xia Zhao2.   

Abstract

A novel triphenylphosphine-mediated direct trifluoromethylthiolation of indole derivatives using trifluoromethanesulfonyl chloride as the SCF3 source was developed. Sodium iodide facilitated this transformation by generating iodine in situ which was found to accelerate this transformation. The use of a transition metal-free protocol, readily available reagents, and mild reaction conditions allowed this protocol to be easily scaled up.

Entities:  

Year:  2017        PMID: 28098311     DOI: 10.1039/c6ob02465c

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  4 in total

1.  Organophosphorus-Catalyzed Deoxygenation of Sulfonyl Chlorides: Electrophilic (Fluoroalkyl)sulfenylation by PIII /PV =O Redox Cycling.

Authors:  Avipsa Ghosh; Morgan Lecomte; Shin-Ho Kim-Lee; Alexander T Radosevich
Journal:  Angew Chem Int Ed Engl       Date:  2019-01-25       Impact factor: 15.336

2.  CF3SO2X (X = Na, Cl) as reagents for trifluoromethylation, trifluoromethylsulfenyl-, -sulfinyl- and -sulfonylation and chlorination. Part 2: Use of CF3SO2Cl.

Authors:  Hélène Chachignon; Hélène Guyon; Dominique Cahard
Journal:  Beilstein J Org Chem       Date:  2017-12-19       Impact factor: 2.883

3.  Tetrabutylammonium Iodide-Promoted Thiolation of Oxindoles Using Sulfonyl Chlorides as Sulfenylation Reagents.

Authors:  Xia Zhao; Aoqi Wei; Xiaoyu Lu; Kui Lu
Journal:  Molecules       Date:  2017-08-01       Impact factor: 4.411

4.  Metal-Free Trifluoromethylthiolation of Arylazo Sulfones.

Authors:  Ankun Li; Yuxuan Li; Junjie Liu; Jingqi Chen; Kui Lu; Di Qiu; Maurizio Fagnoni; Stefano Protti; Xia Zhao
Journal:  J Org Chem       Date:  2020-12-22       Impact factor: 4.354

  4 in total

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