Effect of 2-Substituents on Allyl-Supported Precatalysts for the Suzuki–Miyaura Reaction: Relating Catalytic Efficiency to the Stability of Palladium(I) Bridging Allyl Dimers-Reference-Cited by-同舟云学术

Effect of 2-Substituents on Allyl-Supported Precatalysts for the Suzuki–Miyaura Reaction: Relating Catalytic Efficiency to the Stability of Palladium(I) Bridging Allyl Dimers

Published:2014-12-30 Issue:1 Volume:34 Page:381-394
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Hruszkewycz Damian P.¹,Guard Louise M.¹,Balcells David²,Feldman Nicola¹,Hazari Nilay¹,Tilset Mats²

Affiliation:

1. The Department of Chemistry, Yale University, P.O. Box 208107, New Haven, Connecticut 06520, United States and

2. Centre for Theoretical and Computational Chemistry (CTCC), Department of Chemistry, University of Oslo, P.O. Box 1033 Blindern, 0315 Oslo, Norway

Funder

American Chemical Society Petroleum Research Fund

Norwegian Research Council

Marie Curie Fellowship

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om501250y

Reference91 articles.

1. Evolution of a Fourth Generation Catalyst for the Amination and Thioetherification of Aryl Halides

2. Well-Defined N-Heterocyclic Carbenes−Palladium(II) Precatalysts for Cross-Coupling Reactions

3. The Development of Versatile Methods for Palladium-Catalyzed Coupling Reactions of Aryl Electrophiles through the Use of P(t-Bu)3 and PCy3 as Ligands

4. Surveying Sterically Demanding N-Heterocyclic Carbene Ligands with Restricted Flexibility for Palladium-catalyzed Cross-Coupling Reactions

5. Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands

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