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  Acid promoted radical-chain difunctionalization of styrenes with stabilized radicals and (N,O)-nucleophiles

Liu, S., & Klussmann, M. (2020). Acid promoted radical-chain difunctionalization of styrenes with stabilized radicals and (N,O)-nucleophiles. Chemical Communications, 56(10), 1557-1560. doi:10.1039/C9CC09369A.

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Item Permalink: https://hdl.handle.net/21.11116/0000-0005-DB4C-0 Version Permalink: https://hdl.handle.net/21.11116/0000-0005-DB4D-F
Genre: Journal Article

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 Creators:
Liu, Sensheng1, Author           
Klussmann, Martin1, Author           
Affiliations:
1Research Group Klußmann, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445608              

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 Abstract: A difunctionalization of alkenes through sequential addition of a radical and a nucleophile has been developed, which is suggested to proceed by a radical chain mechanism not requiring a catalyst. An electron transfer step to the oxidant benzoyl peroxide is facilitated by protonation with a strong acid.

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Language(s): eng - English
 Dates: 2019-12-022020-01-072020-01-072020-02-04
 Publication Status: Issued
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1039/C9CC09369A
 Degree: -

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Title: Chemical Communications
  Other : Chem. Commun.
Source Genre: Journal
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Publ. Info: Cambridge, UK : Royal Society of Chemistry
Pages: - Volume / Issue: 56 (10) Sequence Number: - Start / End Page: 1557 - 1560 Identifier: ISSN: 1359-7345
CoNE: https://pure.mpg.de/cone/journals/resource/954928495413