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  Multiply chiral phosphite/phosphonite ligands: tuning enantioselectivity by choice of diastereomers

Reetz, M. T., & Maiwald, P. (2002). Multiply chiral phosphite/phosphonite ligands: tuning enantioselectivity by choice of diastereomers. Comptes Rendus Chimie, 5(4), 341-344. doi:10.1016/S1631-0748(02)01381-4.

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 Creators:
Reetz, M. T.1, Author           
Maiwald, P.1, Author           
Affiliations:
1Research Department Reetz, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445588              

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Free keywords: asymmetric catalysis; phosphites; phosphonites; transition metals; enantioselectivity
 Abstract: Starting from commercially available (S)-1-(2- bromophenyl)ethanol, novel phosphite/phosphonite ligands have been prepared in which a BINOL moiety is attached to each phosphorus centre. The four diasteromeric ligands were tested in Cu-catalysed conjugate addition of Et2Zn, Pd-catalysed allylic substitution and Rh-catalysed hydrogenation. Very different results regarding activity and enantioselectivity as a function of the particular diastereomer were observed. (C) 2002 Academie des sciences / Editions scientifiques et medicales Elsevier SAS.

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Language(s): eng - English
 Dates: 2002-04
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 19872
DOI: 10.1016/S1631-0748(02)01381-4
ISI: 000177497200018
 Degree: -

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Title: Comptes Rendus Chimie
  Alternative Title : C. R. Chim.
Source Genre: Journal
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Publ. Info: -
Pages: - Volume / Issue: 5 (4) Sequence Number: - Start / End Page: 341 - 344 Identifier: ISSN: 1631-0748