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  Stereoselective [2,3]-sigmatropic rearrangement of chiral amine oxides derived from amino acids

Reetz, M. T., & Lauterbach, E. H. (1991). Stereoselective [2,3]-sigmatropic rearrangement of chiral amine oxides derived from amino acids. Tetrahedron Letters, 32(35), 4481-4482. doi:10.1016/0040-4039(91)80017-Z.

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Item Permalink: https://hdl.handle.net/21.11116/0000-000E-7B1D-9 Version Permalink: https://hdl.handle.net/21.11116/0000-000E-7B1E-8
Genre: Journal Article

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 Creators:
Reetz, M. T.1, Author           
Lauterbach, E. H.1, Author
Affiliations:
1Philipps-Universität Marburg, Fachbereich Chemie, Hans-Meerwein-Straße, Marburg, ou_persistent22              

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Free keywords: Amino acids; amine oxides; [2;3]-sigmatropic rearrangement; diastereoselectivity
 Abstract: Chiral γ-N,N-dibenzylamino, α,β-unsaturated esters 1 are oxidized by m-chloro perbenzoic acid to form the amine oxides 2 which undergo a [2,3]-sigmatropic rearrangement with complete 1,3-transfer of chirality.

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Language(s): eng - English
 Dates: 1991-05-281991
 Publication Status: Issued
 Pages: 2
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1016/0040-4039(91)80017-Z
 Degree: -

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Title: Tetrahedron Letters
  Abbreviation : Tetrahedron Lett.
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: Oxford : Pergamon
Pages: - Volume / Issue: 32 (35) Sequence Number: - Start / End Page: 4481 - 4482 Identifier: ISSN: 0040-4039
CoNE: https://pure.mpg.de/cone/journals/resource/954925448772