A highly active and recyclable homogeneous NHC–palladium catalyst with pH- and light-sensitive tags for the Suzuki–Miyaura coupling reactions of aryl halides with arylboronic acids

RSC Advances ◽  
2016 ◽  
Vol 6 (50) ◽  
pp. 44475-44479 ◽  
Author(s):  
Guiyan Liu ◽  
Chengxin Liu ◽  
Xia Zhao ◽  
Jianhui Wang

A highly active and recyclable homogeneous NHC–palladium catalyst for the Suzuki–Miyaura coupling reactions is reported. By making use of the pH- and light-sensitive SP tags, the catalyst can be recovered and reused nine times.

RSC Advances ◽  
2021 ◽  
Vol 11 (43) ◽  
pp. 26883-26891
Author(s):  
Jairus L. Lamola ◽  
Paseka T. Moshapo ◽  
Cedric W. Holzapfel ◽  
Munaka Christopher Maumela

Efficient palladium catalyst systems consisting of bench-stable biaryl phosphacycles and Pd(OAc)2 are described for Suzuki–Miyaura cross-coupling reactions of a diverse array of aryl halides and arylboronic acids.


RSC Advances ◽  
2015 ◽  
Vol 5 (2) ◽  
pp. 1295-1300 ◽  
Author(s):  
Shaheen M. Sarkar ◽  
Md. Lutfor Rahman ◽  
Mashitah Mohd Yusoff

SBA-15 supported heterogeneous Pd-catalyst was prepared and applied towards Sonogashira and Suzuki–Miyaura cross-coupling reactions of activated and inactivated aryl halides to give the corresponding coupling products in up to 98% yield.


RSC Advances ◽  
2015 ◽  
Vol 5 (25) ◽  
pp. 19630-19637 ◽  
Author(s):  
Shaheen M. Sarkar ◽  
Md. Lutfor Rahman ◽  
Mashitah Mohd Yusoff

Pyridinyl functionalized MCM-48-supported Pd-catalyst efficiently (0.013–0.025 mol%) promoted Heck, Suzuki and Sonogashira cross-coupling reactions. Moreover, the catalyst was reused five times without significant loss of its activity.


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