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  Meerwein-type Bromoarylation with Arylthianthrenium Salts

Cai, Y., & Ritter, T. (2022). Meerwein-type Bromoarylation with Arylthianthrenium Salts. Angewandte Chemie, International Edition, 61(47): e202209882. doi:10.1002/anie.202209882.

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 Creators:
Cai, Yuan1, Author           
Ritter, Tobias1, Author           
Affiliations:
1Research Department Ritter, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_2040308              

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Free keywords: Arylthianthrenium Salts; Bromoarylation of Alkenes; Late-Stage Functionalization; Meerwein Arylation
 Abstract: Herein, we report a photocatalyzed Meerwein-type bromoarylation of alkenes with stable arylthianthrenium salts, formed by site-selective C−H thianthrenation. This protocol can be applied to late-stage functionalization of a variety of biomolecules that are difficult to access by other aryl coupling reagents. Halogen introduction allows for a variety of follow-up transformations, affording numerous biologically active skeletons.

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Language(s): eng - English
 Dates: 2022-07-062022-09-072022-11-21
 Publication Status: Issued
 Pages: 5
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1002/anie.202209882
 Degree: -

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Title: Angewandte Chemie, International Edition
  Abbreviation : Angew. Chem., Int. Ed.
Source Genre: Journal
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Publ. Info: Weinheim : Wiley-VCH
Pages: - Volume / Issue: 61 (47) Sequence Number: e202209882 Start / End Page: - Identifier: ISSN: 1433-7851
CoNE: https://pure.mpg.de/cone/journals/resource/1433-7851