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  Reagent control in the aldol addition of chiral boron enolates based on the 2,5-diphenylborolane ligand system

Reetz, M. T., Rivadeneira, E., & Niemeyer, C. (1990). Reagent control in the aldol addition of chiral boron enolates based on the 2,5-diphenylborolane ligand system. Tetrahedron Letters, 31(27), 3863-3866. doi:10.1016/S0040-4039(00)97489-6.

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Item Permalink: https://hdl.handle.net/21.11116/0000-000E-7CCB-3 Version Permalink: https://hdl.handle.net/21.11116/0000-000E-7CCC-2
Genre: Journal Article

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Reetz, M. T.1, Author           
Rivadeneira, E.1, Author
Niemeyer, C.1, Author
Affiliations:
1Philipps-Universität Marburg, Fachbereich Chemie, Hans-Meerwein-Straße, Marburg, ou_persistent22              

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 Abstract: Thioesters can be O-borylated using optically active chloro-2,5-diphenylborolane to produce chiral boron enolates which show complete reagent control in aldol additions to chiral α-amino aldehydes.
Boron enolates of the type 2 add to chiral α-amino aldehydes with essentially complete reagent control to form aldol adducts.

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Language(s): eng - English
 Dates: 1990-05-051990
 Publication Status: Issued
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1016/S0040-4039(00)97489-6
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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: 31 (27) Sequence Number: - Start / End Page: 3863 - 3866 Identifier: ISSN: 0040-4039
CoNE: https://pure.mpg.de/cone/journals/resource/954925448772