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  C–H carbonylation: In situ acyl triflates ace it

Lee, Y. H., & Morandi, B. (2018). C–H carbonylation: In situ acyl triflates ace it. Nature Chemistry, 10(2), 116-117. doi:10.1038/nchem.2934.

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 Creators:
Lee, Yong Ho1, Author           
Morandi, Bill1, Author           
Affiliations:
1Research Group Morandi, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_2040309              

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Free keywords: Homogeneous catalysis; Synthetic chemistry methodology
 Abstract: A simple palladium catalyst has mediated the facile formation of aroyl triflates — an extremely reactive class of electrophiles. These intermediates, generated in situ, enable the Friedel–Crafts acylation of traditionally unreactive arenes, addressing a significant gap in C–H carbonylation methodology.

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Language(s): eng - English
 Dates: 2018-01-232018-02-01
 Publication Status: Published in print
 Pages: 2
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1038/nchem.2934
 Degree: -

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Title: Nature Chemistry
  Abbreviation : Nat. Chem.
Source Genre: Journal
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Publ. Info: London, UK : Nature Publishing Group
Pages: - Volume / Issue: 10 (2) Sequence Number: - Start / End Page: 116 - 117 Identifier: ISSN: 1755-4330
CoNE: https://pure.mpg.de/cone/journals/resource/1755-4330