Literature DB >> 29024259

Selective Radical Fluorination of Tertiary Alkyl Halides at Room Temperature.

He Chen1, Zhonglin Liu1, Ying Lv2, Xinqiang Tan1, Haigen Shen1, Hai-Zhu Yu2, Chaozhong Li1,3.   

Abstract

Direct fluorination of tertiary alkyl bromides and iodides with Selectfluor is described. The halogen-exchange fluorination proceeds efficiently in acetonitrile at room temperature under metal-free conditions and exhibits a wide range of functional group compatibility. Furthermore, the reactions are highly selective in that alkyl chlorides and primary and secondary alkyl bromides remain intact. A radical mechanism is proposed for this selective fluorination.
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  alkyl halides; fluorination; halogen exchange; radicals; synthetic methods

Year:  2017        PMID: 29024259     DOI: 10.1002/anie.201708197

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  3 in total

1.  Manganese/bipyridine-catalyzed non-directed C(sp3)-H bromination using NBS and TMSN3.

Authors:  Kumar Sneh; Takeru Torigoe; Yoichiro Kuninobu
Journal:  Beilstein J Org Chem       Date:  2021-04-22       Impact factor: 2.883

Review 2.  Photosensitized direct C-H fluorination and trifluoromethylation in organic synthesis.

Authors:  Shahboz Yakubov; Joshua P Barham
Journal:  Beilstein J Org Chem       Date:  2020-09-03       Impact factor: 2.883

3.  A third generation of radical fluorinating agents based on N-fluoro-N-arylsulfonamides.

Authors:  Daniel Meyer; Harish Jangra; Fabian Walther; Hendrik Zipse; Philippe Renaud
Journal:  Nat Commun       Date:  2018-11-20       Impact factor: 14.919

  3 in total

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