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  A Brønsted Acid Catalyzed Redox Arylation

Peng, B., Huang, X., Xie, L., & Maulide, N. (2014). A Brønsted Acid Catalyzed Redox Arylation. Angewandte Chemie, International Edition, 53(33), 8718-8721. doi:10.1002/anie.201310865.

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 Creators:
Peng, Bo1, Author              
Huang, Xueliang1, Author              
Xie, Langui1, Author              
Maulide, Nuno1, Author              
Affiliations:
1Research Group Maulide, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445614              

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Free keywords: CLAISEN REARRANGEMENT SEQUENCE; NUCLEOPHILIC ORTHO-ALLYLATION; SAUCY-MARBET REARRANGEMENT; C-H FUNCTIONALIZATION; CARBONYL-COMPOUNDS; ALPHA-ARYLATION; METAL-FREE; ELECTROPHILIC REARRANGEMENTS; EFFICIENT SYNTHESIS; ORGANIC-SYNTHESIS
 Abstract: A Brønsted acid catalyzed redox arylation of ynamides that employs aryl sulfoxides as the arylating agents is reported. This metal-free transformation proceeds at room temperature and efficiently affords α-arylated oxazolidinones in a redox-neutral, atom-economic fashion.

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Language(s): eng - English
 Dates: 2014-03-032014-08-11
 Publication Status: Published in print
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1002/anie.201310865
 Degree: -

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Title: Angewandte Chemie, International Edition
  Other : Angew. Chem., Int. Ed.
  Other : Angew. Chem. Int. Ed
  Other : Angewandte Chemie International Edition
  Abbreviation : Angew. Chem. Int. Ed
Source Genre: Journal
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Publ. Info: Weinheim, Deutschland : Viley-VCH
Pages: - Volume / Issue: 53 (33) Sequence Number: - Start / End Page: 8718 - 8721 Identifier: CoNE: https://pure.mpg.de/cone/journals/resource/1433-7851