Pyrazole-tethered arylphosphine ligands for Suzuki reactions of aryl chlorides: how important is chelation?

2004 ◽  
Vol 45 (52) ◽  
pp. 9525-9528 ◽  
Author(s):  
Anuradha Mukherjee ◽  
Amitabha Sarkar
Keyword(s):  
Aryl Chlorides ◽  
Suzuki Reactions

General and User-friendly Method for Suzuki Reactions with Aryl Chlorides

Synlett ◽  
2001 ◽  
Vol 2001 (02) ◽  
pp. 0290-0292 ◽  
Author(s):  
Alois Fürstner ◽  
Andreas Leitner
Keyword(s):  
Aryl Chlorides ◽  
Suzuki Reactions ◽  
User Friendly

Microwave-Promoted Suzuki Reactions of Aryl Chlorides in Aqueous Media

2005 ◽  
Vol 70 (6) ◽  
pp. 2332-2334 ◽  
Author(s):  
Guobin Miao ◽  
Ping Ye ◽  
Libing Yu ◽  
Carmen M. Baldino
Keyword(s):  
Aqueous Media ◽  
Aryl Chlorides ◽  
Suzuki Reactions

In situ generated palladium catalysts bearing 1,3-dialkylperimidin-2-yline ligands for Suzuki reactions of aryl chlorides

2004 ◽  
Vol 217 (1-2) ◽  
pp. 37-40 ◽  
Author(s):  
İsmail Özdemir ◽  
Bülent Alıcı ◽  
Nevin Gürbüz ◽  
Engin Çetinkaya ◽  
Bekir Çetinkaya
Keyword(s):  
Palladium Catalysts ◽  
Aryl Chlorides ◽  
Suzuki Reactions

scholarly journals Microwave-Promoted Suzuki Reactions of Aryl Chlorides in Aqueous Media.

ChemInform ◽  
2005 ◽  
Vol 36 (33) ◽  
Author(s):  
Guobin Miao ◽  
Ping Ye ◽  
Libing Yu ◽  
Carmen M. Baldino
Keyword(s):  
Aqueous Media ◽  
Aryl Chlorides ◽  
Suzuki Reactions

scholarly journals Bulky Di(1-adamantyl)phosphinous Acid-Ligated Pd(II) Precatalysts for Suzuki Reactions of Unreactive Aryl Chlorides

ACS Omega ◽  
2021 ◽  
Author(s):  
He-Xin Xiao ◽  
Wan-Yun Hsu ◽  
Siou-Wei Liang ◽  
Yingjie Guo ◽  
Wan-Ching Lee ◽  
...  
Keyword(s):  
Phosphinous Acid ◽  
Aryl Chlorides ◽  
Suzuki Reactions

Pd-Catalyzed Suzuki coupling reactions of aryl halides containing basic nitrogen centers with arylboronic acids in water in the absence of added base

2017 ◽  
Vol 41 (24) ◽  
pp. 15420-15432 ◽  
Author(s):  
Zhao Li ◽  
Carol Gelbaum ◽  
Zachary S. Campbell ◽  
Paul C. Gould ◽  
Jason S. Fisk ◽  
...  
Keyword(s):  
Suzuki Coupling ◽  
Aryl Halides ◽  
Coupling Reactions ◽  
Aryl Chlorides ◽  
Arylboronic Acids ◽  
Suzuki Reactions ◽  
Basic Nitrogen ◽  
Acidic Conditions

Successful Suzuki reactions of basic nitrogen containing aryl chlorides/bromides with arylboronic acids in water without added base, partially or entirely under acidic conditions.

Chiral Mn(III) Salen Complex Immobilized on CuFe2O4@SiO2-NH2 NPs: A Cheap and Efficient Catalyst for N-arylation of Aryl Halides and Phenylboronic Acid Under Mild Conditions

2020 ◽  
Vol 17 (11) ◽  
pp. 857-863
Author(s):  
Mohammad Ali Nasseri ◽  
Seyyedeh Ameneh Alavi ◽  
Milad Kazemnejadi ◽  
Ali Allahresani
Keyword(s):  
Phenylboronic Acid ◽  
Significant Loss ◽  
Aryl Halides ◽  
Coupling Reactions ◽  
Efficient Catalyst ◽  
Aryl Chlorides ◽  
Mild Conditions ◽  
Cross Coupling Reactions ◽  
Salen Complex ◽  
Ft Ir

A convenient and efficient chiral CuFe2O4@SiO2-Mn(III) Ch.salen nanocatalyst has been developed for the C-N cross-coupling reactions of aryl halides/ phenylboronic acid with N-heterocyclic compounds in water and/or DMSO under mild conditions. The catalyst could be applied for the N-arylation of a variety of nitrogen-containing heterocycles with aryl chlorides, bromides, iodides and phenylboronic acid under mild conditions. Moderate to good yields were achieved for all substrates. The structure of catalyst was characterized using various techniques including FT-IR, FE-SEM, EDX, XRD, TEM and TGA. The catalyst can be simply recovered and reused for several times without significant loss of activity.

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