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  Facile Hydride Ion Abstraction from Enamines, Allylamines and Imines

Reetz, M. T., Stephan, W., & Maier, W. F. (1980). Facile Hydride Ion Abstraction from Enamines, Allylamines and Imines. Synthetic Communications, 10(11), 867-871. doi:10.1080/00397918008062771.

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Item Permalink: https://hdl.handle.net/21.11116/0000-000E-A5AA-8 Version Permalink: https://hdl.handle.net/21.11116/0000-000E-A5AB-7
Genre: Journal Article

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 Creators:
Reetz, M. T.1, Author           
Stephan, W.1, Author
Maier, W. F.1, Author
Affiliations:
1Philipps-Universität Marburg, Fachbereich Chemie, Hans-Meerwein-Straße, Marburg, ou_persistent22              

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 Abstract: The conversion of tertiary amines to iminium ions has been accomplished with such oxidants as mercuric acetate or trityl salts2. We wish to report that hydride ion abstraction can be applied to enamines, allylamines and imines. Treatment of 1 or 3 with trityl tetrafluoroborate (⊘ = phenyl) affords 2 in yields of 91% and 63%, respectively.

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Language(s): eng - English
 Dates: 1980-11-01
 Publication Status: Issued
 Pages: 5
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1080/00397918008062771
 Degree: -

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Title: Synthetic Communications
  Abbreviation : Synth. Commun.
Source Genre: Journal
 Creator(s):
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Publ. Info: [New York : M. Dekker]
Pages: - Volume / Issue: 10 (11) Sequence Number: - Start / End Page: 867 - 871 Identifier: ISSN: 0039-7911
CoNE: https://pure.mpg.de/cone/journals/resource/954925448758