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  Enantioselective addition of chirally modified methyltitanium reagents to aromatic aldehydes

Reetz, M. T., Kükenhöhner, T., & Weinig, P. (1986). Enantioselective addition of chirally modified methyltitanium reagents to aromatic aldehydes. Tetrahedron Letters, 27(47), 5711-5714. doi:10.1016/S0040-4039(00)85307-1.

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Item Permalink: https://hdl.handle.net/21.11116/0000-000E-7E51-A Version Permalink: https://hdl.handle.net/21.11116/0000-000E-7E52-9
Genre: Journal Article

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 Creators:
Reetz, M. T.1, Author           
Kükenhöhner, T.1, Author
Weinig, P.1, Author
Affiliations:
1Philipps-Universität Marburg, Fachbereich Chemie, Hans-Meerwein-Straße, Marburg, ou_persistent22              

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 Abstract: N-Sulfonylated derivatives of norephedrine are excellent ligands for chirally modified methyltitanium reagents, the latter reacting enantioselectively with aromatic aldehydes (ee ~ 90%) to form R-configurated carbinols.

The oligomeric form of 2 reacts enantioselectively with aromatic aldehydes to form having ee ~ 90%.

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Language(s): eng - English
 Dates: 1986-08-291986
 Publication Status: Issued
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1016/S0040-4039(00)85307-1
 Degree: -

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Title: Tetrahedron Letters
  Abbreviation : Tetrahedron Lett.
Source Genre: Journal
 Creator(s):
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Publ. Info: Oxford : Pergamon
Pages: - Volume / Issue: 27 (47) Sequence Number: - Start / End Page: 5711 - 5714 Identifier: ISSN: 0040-4039
CoNE: https://pure.mpg.de/cone/journals/resource/954925448772