A superior P-H phosphonite: Asymmetric allylic substitutions with fenchol-based palladium catalysts
The fenchol-based P-H phosphonite BIFOP-H exeeds with 65% ee other monodentate ligands in the Pd-catalyzed substitution of 1-phenyl-2-propenyl acetate with dimethylmalonate.
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
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Beilstein-Institut
2006-03-01
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Series: | Beilstein Journal of Organic Chemistry |
Online Access: | https://doi.org/10.1186/1860-5397-2-7 |
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author | Bernd Goldfuss Thomas Löschmann Tina Kop-Weiershausen Jörg Neudörfl Frank Rominger |
author_facet | Bernd Goldfuss Thomas Löschmann Tina Kop-Weiershausen Jörg Neudörfl Frank Rominger |
author_sort | Bernd Goldfuss |
collection | DOAJ |
description | The fenchol-based P-H phosphonite BIFOP-H exeeds with 65% ee other monodentate ligands in the Pd-catalyzed substitution of 1-phenyl-2-propenyl acetate with dimethylmalonate. |
first_indexed | 2024-12-22T09:38:06Z |
format | Article |
id | doaj.art-ecc71fb553ce491fbdb5cc34b8c78b10 |
institution | Directory Open Access Journal |
issn | 1860-5397 |
language | English |
last_indexed | 2024-12-22T09:38:06Z |
publishDate | 2006-03-01 |
publisher | Beilstein-Institut |
record_format | Article |
series | Beilstein Journal of Organic Chemistry |
spelling | doaj.art-ecc71fb553ce491fbdb5cc34b8c78b102022-12-21T18:30:46ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972006-03-0121710.1186/1860-5397-2-71860-5397-2-7A superior P-H phosphonite: Asymmetric allylic substitutions with fenchol-based palladium catalystsBernd Goldfuss0Thomas Löschmann1Tina Kop-Weiershausen2Jörg Neudörfl3Frank Rominger4Institut für Organische Chemie, Universität zu Köln, Greinstraße 4, D-50939 Köln, GermanyDottikon Exclusive Synthesis, Hembrunnstrasse 17, CH-5605 Dottikon, SwitzerlandInstitut für Organische Chemie, Universität zu Köln, Greinstraße 4, D-50939 Köln, GermanyInstitut für Organische Chemie, Universität zu Köln, Greinstraße 4, D-50939 Köln, GermanyX-ray analysesThe fenchol-based P-H phosphonite BIFOP-H exeeds with 65% ee other monodentate ligands in the Pd-catalyzed substitution of 1-phenyl-2-propenyl acetate with dimethylmalonate.https://doi.org/10.1186/1860-5397-2-7 |
spellingShingle | Bernd Goldfuss Thomas Löschmann Tina Kop-Weiershausen Jörg Neudörfl Frank Rominger A superior P-H phosphonite: Asymmetric allylic substitutions with fenchol-based palladium catalysts Beilstein Journal of Organic Chemistry |
title | A superior P-H phosphonite: Asymmetric allylic substitutions with fenchol-based palladium catalysts |
title_full | A superior P-H phosphonite: Asymmetric allylic substitutions with fenchol-based palladium catalysts |
title_fullStr | A superior P-H phosphonite: Asymmetric allylic substitutions with fenchol-based palladium catalysts |
title_full_unstemmed | A superior P-H phosphonite: Asymmetric allylic substitutions with fenchol-based palladium catalysts |
title_short | A superior P-H phosphonite: Asymmetric allylic substitutions with fenchol-based palladium catalysts |
title_sort | superior p h phosphonite asymmetric allylic substitutions with fenchol based palladium catalysts |
url | https://doi.org/10.1186/1860-5397-2-7 |
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