Reversal of aryl bromide reactivity in Pd-catalysed aryl amination reactions promoted by a hemilabile aminophosphine ligand-Reference-Cited by-同舟云学术

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Reversal of aryl bromide reactivity in Pd-catalysed aryl amination reactions promoted by a hemilabile aminophosphine ligand

Published:2005-10 Issue:41 Volume:61 Page:9822-9826
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Parisel Sebastien L.,Adrio Luis Angel,Pereira Adriana Amoedo,Pérez Marta Marino,Vila José M.,Hii King Kuok (Mimi)

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference23 articles.

1. Monoligated Palladium Species as Catalysts in Cross-Coupling Reactions

2. Syntheses and Properties of Palladium Complexes Containing Phosphorus−Nitrogen−Phosphorus Ligands with a Tunable Hemilabile Site

3. Examining the effect of hemilabile donor groups in non-C2 symmetrical terdentate ligands

4. Phosphorus–nitrogen–phosphorus ligands: cooperative effects between nitrogen and phosphorus substituents on catalytic activity

5. Examination of Ligand Effects in the Heck Arylation Reaction

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