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.

Detalles Bibliográficos
Autores principales: Goldfuss, Bernd, Löschmann, Thomas, Kop-Weiershausen, Tina, Neudörfl, Jörg, Rominger, Frank
Formato: Texto
Lenguaje:English
Publicado: Beilstein-Institut 2006
Materias:
Full Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1479457/
https://www.ncbi.nlm.nih.gov/pubmed/16573833
http://dx.doi.org/10.1186/1860-5397-2-7
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author Goldfuss, Bernd
Löschmann, Thomas
Kop-Weiershausen, Tina
Neudörfl, Jörg
Rominger, Frank
author_facet Goldfuss, Bernd
Löschmann, Thomas
Kop-Weiershausen, Tina
Neudörfl, Jörg
Rominger, Frank
author_sort Goldfuss, Bernd
collection PubMed
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.
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spelling pubmed-14794572006-06-16 A superior P-H phosphonite: Asymmetric allylic substitutions with fenchol-based palladium catalysts Goldfuss, Bernd Löschmann, Thomas Kop-Weiershausen, Tina Neudörfl, Jörg Rominger, Frank Beilstein J Org Chem Full Research Paper 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. Beilstein-Institut 2006-03-30 /pmc/articles/PMC1479457/ /pubmed/16573833 http://dx.doi.org/10.1186/1860-5397-2-7 Text en Copyright © 2006, Goldfuss et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Goldfuss, Bernd
Löschmann, Thomas
Kop-Weiershausen, Tina
Neudörfl, Jörg
Rominger, Frank
A superior P-H phosphonite: Asymmetric allylic substitutions with fenchol-based palladium catalysts
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
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1479457/
https://www.ncbi.nlm.nih.gov/pubmed/16573833
http://dx.doi.org/10.1186/1860-5397-2-7
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