Versatile Catalysts for the Suzuki Cross-Coupling of Arylboronic Acids with Aryl and Vinyl Halides and Triflates under Mild Conditions

2000 ◽  
Vol 122 (17) ◽  
pp. 4020-4028 ◽  
Author(s):  
Adam F. Littke ◽  
Chaoyang Dai ◽  
Gregory C. Fu
Keyword(s):  
Cross Coupling ◽  
Arylboronic Acids ◽  
Vinyl Halides ◽  
Mild Conditions

Efficient symmetrical bidentate dioxime ligand-accelerated homogeneous palladium-catalyzed Suzuki–Miyaura coupling reactions of aryl chlorides

2017 ◽  
Vol 41 (1) ◽  
pp. 372-376 ◽  
Author(s):  
Jinyi Song ◽  
Hongyan Zhao ◽  
Yang Liu ◽  
Huatao Han ◽  
Zhuofei Li ◽  
...  
Keyword(s):  
High Activity ◽  
Cross Coupling ◽  
Coupling Reactions ◽  
Bidentate Ligands ◽  
Aryl Chlorides ◽  
Arylboronic Acids ◽  
Mild Conditions ◽  
Cross Coupling Reactions ◽  
Palladium Catalyzed

A series of N,O-bidentate ligands were synthesized and studied as high activity ligands for palladium-catalyzed Suzuki–Miyaura cross-coupling reactions of aryl chlorides with arylboronic acids under mild conditions.

Novel α-arylnitriles synthesis via Ni-catalyzed cross-coupling of α-bromonitriles with arylboronic acids under mild conditions

2011 ◽  
Vol 9 (15) ◽  
pp. 5343 ◽  
Author(s):  
Yingying Yang ◽  
Shan Tang ◽  
Chao Liu ◽  
Huimin Zhang ◽  
Zhexun Sun ◽  
...  
Keyword(s):  
Cross Coupling ◽  
Arylboronic Acids ◽  
Mild Conditions

Gold-catalysed cross-coupling between aryldiazonium salts and arylboronic acids: probing the usefulness of photoredox conditions

2016 ◽  
Vol 52 (65) ◽  
pp. 10040-10043 ◽  
Author(s):  
Thomas Cornilleau ◽  
Philippe Hermange ◽  
Eric Fouquet
Keyword(s):  
Cross Coupling ◽  
Gold Catalysis ◽  
Boronic Acids ◽  
Diazonium Salts ◽  
Arylboronic Acids ◽  
Mild Conditions ◽  
Biaryl Compounds

Combining gold catalysis and photoredox processes allowed the synthesis of biaryl compounds from diazonium salts and boronic acids under mild conditions.

Nickel-catalyzed cross-coupling of carboxylic anhydrides with arylboronic acids

RSC Advances ◽  
2014 ◽  
Vol 4 (96) ◽  
pp. 53885-53890 ◽  
Author(s):  
Qiang Chen ◽  
Xin-Heng Fan ◽  
Li-Peng Zhang ◽  
Lian-Ming Yang
Keyword(s):  
Cross Coupling ◽  
Arylboronic Acids ◽  
Mild Conditions ◽  
The Cross

A nickel-based catalyst was employed in the cross-coupling of carboxylic anhydrides with arylboronic acids, and various products were achieved in good yields under mild conditions.

Ni(ii) source as a pre-catalyst for the cross-coupling of benzylic pivalates with arylboronic acids: facile access to tri- and diarylmethanes

RSC Advances ◽  
2015 ◽  
Vol 5 (20) ◽  
pp. 15338-15340 ◽  
Author(s):  
Qiang Chen ◽  
Xin-Heng Fan ◽  
Li-Peng Zhang ◽  
Lian-Ming Yang
Keyword(s):  
Cross Coupling ◽  
Arylboronic Acids ◽  
Mild Conditions ◽  
The Cross ◽  
Benzylic Pivalates

Various di- and triarylmethanes were synthesized via NiII–(σ-aryl) complex-catalyzed Suzuki–Miyaura cross-coupling of benzylic pivalates with arylboronic acids under mild conditions.

scholarly journals Au(I)/Au(III)-catalyzed Sonogashira-type reactions of functionalized terminal alkynes with arylboronic acids under mild conditions

2011 ◽  
Vol 7 ◽  
pp. 808-812 ◽  
Author(s):  
Deyun Qian ◽  
Junliang Zhang
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
Catalyst System ◽  
Terminal Alkynes ◽  
Arylboronic Acids ◽  
Mild Conditions ◽  
Redox Catalyst ◽  
Cross Coupling Reaction

A straightforward, efficient, and reliable redox catalyst system for the Au(I)/Au(III)-catalyzed Sonogashira cross-coupling reaction of functionalized terminal alkynes with arylboronic acids under mild conditions has been developed.

C–Te Cross-Coupling of Diaryl Ditellurides with Arylboronic Acids by Using Copper(I) Thiophene-2-carboxylate under Mild Conditions

Synlett ◽  
2018 ◽  
Vol 30 (01) ◽  
pp. 99-103 ◽  
Author(s):  
Shinichi Koguchi ◽  
Yuga Shibuya ◽  
Yusuke Igarashi ◽  
Haruka Takemura
Keyword(s):  
Room Temperature ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Polar Solvents ◽  
Arylboronic Acids ◽  
Mild Conditions ◽  
Cross Coupling Reaction ◽  
Neutral Conditions

We describe the successful cross-coupling of diaryl ditellurides with arylboronic acids by using copper(I) thiophene-2-carboxylate (CuTC) under mild conditions. Although other studies have reported that highly polar solvents (such as DMSO) or bases are required, this reaction was completed by using CuTC and common solvents under neutral conditions at room temperature. This cross-coupling reaction was performed with diaryl ditellurides and arylboronic acids bearing various groups, affording the corresponding diaryl tellurides in good to excellent yields.

ChemInform Abstract: Novel α-Arylnitriles Synthesis via Ni-Catalyzed Cross-Coupling of α-Bromonitriles with Arylboronic Acids under Mild Conditions.

ChemInform ◽  
2011 ◽  
Vol 42 (48) ◽  
pp. no-no
Author(s):  
Yingying Yang ◽  
Shan Tang ◽  
Chao Liu ◽  
Huimin Zhang ◽  
Zhexun Sun ◽  
...  
Keyword(s):  
Cross Coupling ◽  
Arylboronic Acids ◽  
Mild Conditions

Highly active NHC–Pd(ii) complexes for cross coupling of aryl chlorides and arylboronic acids: an investigation of the effect of remote bulky groups

2018 ◽  
Vol 42 (9) ◽  
pp. 7422-7427 ◽  
Author(s):  
Fangwai Han ◽  
Ying Xu ◽  
Rongjiao Zhu ◽  
Guiyan Liu ◽  
Chen Chen ◽  
...  
Keyword(s):  
Cross Coupling ◽  
Coupling Reactions ◽  
Aryl Chlorides ◽  
Arylboronic Acids ◽  
Mild Conditions ◽  
Highly Active ◽  
Bulky Ligands

Highly active palladium(ii) complexes bearing remote bulky ligands for Suzuki–Miyaura coupling reactions under mild conditions are reported.

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