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  Palladium-Catalysed Amination of Aryl- and Heteroaryl Halides Using tert-Butyl Tetraisopropylphosphorodiamidite as an Easily Accessible and Air-Stable Ligand

Roiban, G.-D., Mehler, G., & Reetz, M. T. (2014). Palladium-Catalysed Amination of Aryl- and Heteroaryl Halides Using tert-Butyl Tetraisopropylphosphorodiamidite as an Easily Accessible and Air-Stable Ligand. European Journal of Organic Chemistry, 2014(10), 2070-2076. doi:10.1002/ejoc.201301789.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0024-556A-3 Version Permalink: https://hdl.handle.net/11858/00-001M-0000-0024-55AF-7
Genre: Journal Article

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 Creators:
Roiban, Georghe-Doru1, 2, Author           
Mehler, Gerlinde1, Author           
Reetz, Manfred T.1, 2, Author           
Affiliations:
1Research Department Reetz, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445588              
2Philipps-Universität Marburg, Fachbereich Chemie, ou_persistent22              

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Free keywords: Amines; Amination; P ligands; Palladium; Homogeneous catalysis
 Abstract: The phosphorus compound tert-butyl tetraisopropylphosphorodiamidite, prepared from bis(diisopropylamino)chlorophosphine, is an excellent ligand for palladium-catalysed Buchwald–Hartwig amination of aryl- and heteroaryl chlorides and bromides. Based on its ready accessibility and air-stability, this amination protocol is a practical approach to the synthesis of industrially important aryl- and heteroarylamines

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Language(s): eng - English
 Dates: 2014-04
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1002/ejoc.201301789
 Degree: -

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Title: European Journal of Organic Chemistry
  Other : Eur. J. Org. Chem.
Source Genre: Journal
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Publ. Info: -
Pages: - Volume / Issue: 2014 (10) Sequence Number: - Start / End Page: 2070 - 2076 Identifier: ISSN: 1434-193X
CoNE: https://pure.mpg.de/cone/journals/resource/954926953810