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  Novel 1,4-asymmetric induction in nucleophilic 1,2-additions to chiral γ-amino enals

Reetz, M. T., Wang, F., & Harms, K. (1991). Novel 1,4-asymmetric induction in nucleophilic 1,2-additions to chiral γ-amino enals. Journal of the Chemical Society, Chemical Communications, 1991(18), 1309-1311. doi:10.1039/C39910001309.

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Item Permalink: https://hdl.handle.net/21.11116/0000-000E-7B2B-9 Version Permalink: https://hdl.handle.net/21.11116/0000-000E-7B2C-8
Genre: Journal Article

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 Creators:
Reetz, M. T.1, Author           
Wang, Fan1, Author
Harms, K.1, Author
Affiliations:
1Philipps-Universität Marburg, Fachbereich Chemie, Hans-Meerwein-Straße, Marburg, ou_persistent22              

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 Abstract: y-Dibenzylamino enals 3a with the E-configuration derived from amino acids 1 react diastereoselectively with cuprates in an unexpected 1,2-manner, while the analogues 3b with the Z-configuration undergo diastereoselective additions with organolithium reagents.

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Language(s): eng - English
 Dates: 1991-06-251991
 Publication Status: Issued
 Pages: 3
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1039/C39910001309
 Degree: -

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Title: Journal of the Chemical Society, Chemical Communications
  Abbreviation : J. Chem. Soc., Chem. Commun.
Source Genre: Journal
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Affiliations:
Publ. Info: London : The Chemical Society
Pages: - Volume / Issue: 1991 (18) Sequence Number: - Start / End Page: 1309 - 1311 Identifier: ISSN: 0022-4936
CoNE: https://pure.mpg.de/cone/journals/resource/954925278588