Use of a bulky phosphine of weak σ-donicity with palladium as a versatile and highly-active catalytic system: allylation and arylation coupling reactions at 10−1–10−4mol% catalyst loadings of ferrocenyl bis(difurylphosphine)/Pd-Reference-Cited by-同舟云学术

Use of a bulky phosphine of weak σ-donicity with palladium as a versatile and highly-active catalytic system: allylation and arylation coupling reactions at 10−1–10−4mol% catalyst loadings of ferrocenyl bis(difurylphosphine)/Pd

Published:2005-10 Issue:41 Volume:61 Page:9759-9766
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Hierso Jean-Cyrille,Fihri Aziz,Amardeil Régine,Meunier Philippe,Doucet Henri,Santelli Maurice

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference57 articles.

1. Researchers in This Field Still Have Many Challenges in Front of Them, but the Future is Indeed Very Bright

2. 5 Transition metals in organic synthesis

3. High-Turnover Palladium Catalysts in Cross-Coupling and Heck Chemistry: A Critical Overview

4. A Palladium−Ferrocenyl Tetraphosphine System as Catalyst for Suzuki Cross-Coupling and Heck Vinylation of Aryl Halides: Dynamic Behavior of the Palladium/Phosphine Species

5. Catalytic Efficiency of a New Tridentate Ferrocenyl Phosphine Auxiliary: Sonogashira Cross-Coupling Reactions of Alkynes with Aryl Bromides and Chlorides at Low Catalyst Loadings of 10-1 to 10-4 Mol %

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