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  Allylic Amination of Alkenes with Iminothianthrenes to Afford Alkyl Allylamines

Cheng, Q., Chen, J., Lin, S., & Ritter, T. (2020). Allylic Amination of Alkenes with Iminothianthrenes to Afford Alkyl Allylamines. Journal of the American Chemical Society, 142(41), 17287-17293. doi:10.1021/jacs.0c08248.

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Genre: Journal Article

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 Creators:
Cheng, Qiang1, Author              
Chen, Junting1, Author              
Lin, Songyun1, Author              
Ritter, Tobias1, Author              
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1Research Department Ritter, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_2040308              

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 Abstract: Allylic C–H amination is currently accomplished with (sulfon)amides or carbamates. Here we show the first allylic amination that can directly afford alkyl allylamines, enabled by the reactivity of thianthrene-based nitrogen sources that can be prepared from primary amines in a single step.

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Language(s): eng - English
 Dates: 2020-07-312020-10-012020-10-14
 Publication Status: Published in print
 Pages: 7
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1021/jacs.0c08248
 Degree: -

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Title: Journal of the American Chemical Society
  Other : JACS
  Abbreviation : J. Am. Chem. Soc.
Source Genre: Journal
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Publ. Info: Washington, DC : American Chemical Society
Pages: - Volume / Issue: 142 (41) Sequence Number: - Start / End Page: 17287 - 17293 Identifier: ISSN: 0002-7863
CoNE: https://pure.mpg.de/cone/journals/resource/954925376870