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  Non-chelation-control in nucleophilic additions to chiral α- and β-alkoxy aldehydes

Reetz, M. T., & Kesseler, K. (1984). Non-chelation-control in nucleophilic additions to chiral α- and β-alkoxy aldehydes. Journal of the Chemical Society, Chemical Communications, 1984(16), 1079-1080. doi:10.1039/C39840001079.

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Item Permalink: https://hdl.handle.net/21.11116/0000-000E-7FE1-6 Version Permalink: https://hdl.handle.net/21.11116/0000-000E-7FE2-5
Genre: Journal Article

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 Creators:
Reetz, Manfred T.1, Author           
Kesseler, Kurt1, Author
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1Philipps-Universität Marburg, Fachbereich Chemie, Hans-Meerwein-Straße, Marburg, ou_persistent22              

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 Abstract: The addition of two equivalents of gaseous BF3 to to α- and β-alkoxy aldehydes having a centre of chirality at the α-position leads to doubly complexed species which react diastereoselectively with silyl enol ethers and allylsilanes to provide non-chelation-controlled adducts.

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Language(s): eng - English
 Dates: 1984
 Publication Status: Issued
 Pages: 2
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1039/C39840001079
 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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Publ. Info: London : The Chemical Society
Pages: - Volume / Issue: 1984 (16) Sequence Number: - Start / End Page: 1079 - 1080 Identifier: ISSN: 0022-4936
CoNE: https://pure.mpg.de/cone/journals/resource/954925278588