Electron-Rich Trialkyl-Type Dihydro-KITPHOS Monophosphines: Efficient Ligands for Palladium-Catalyzed Suzuki–Miyaura Cross-Coupling. Comparison with Their Biaryl-Like KITPHOS Monophosphine Counterparts-Reference-Cited by-同舟云学术

Electron-Rich Trialkyl-Type Dihydro-KITPHOS Monophosphines: Efficient Ligands for Palladium-Catalyzed Suzuki–Miyaura Cross-Coupling. Comparison with Their Biaryl-Like KITPHOS Monophosphine Counterparts

Published:2013-02-20 Issue:6 Volume:32 Page:1773-1788
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Doherty Simon¹,Knight Julian G.¹,Ward Nicholas A. B.¹,Bittner Dror M.¹,Wills Corinne¹,McFarlane William¹,Clegg William¹,Harrington Ross W.¹

Affiliation:

1. NUCat, School of Chemistry, Bedson Building, Newcastle University, Newcastle upon Tyne NE1 7RU, U.K.

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om3011992

Reference165 articles.

1. 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

2. Biaryl Phosphane Ligands in Palladium-Catalyzed Amination

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

4. Dialkylbiaryl phosphines in Pd-catalyzed amination: a user's guide

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