scholarly journals Scope of the Two-Step, One-Pot Palladium-Catalyzed Borylation/Suzuki Cross-Coupling Reaction Utilizing Bis-Boronic Acid

2012 ◽  
Vol 77 (19) ◽  
pp. 8678-8688 ◽  
Author(s):  
Gary A. Molander ◽  
Sarah L. J. Trice ◽  
Steven M. Kennedy
Keyword(s):  
Boronic Acid ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
One Pot ◽  
Cross Coupling Reaction ◽  
Palladium Catalyzed

scholarly journals Recent Advances in the Applications of the Intramolecular Suzuki Cross-coupling Reaction in Cyclization and Heterocyclization: An Update

2020 ◽  
Vol 23 (22) ◽  
pp. 2469-2488 ◽  
Author(s):  
Majid M. Heravi ◽  
Masoumeh Malmir ◽  
Razieh Moradi
Keyword(s):  
Organic Chemistry ◽  
Boronic Acid ◽  
Heterocyclic Compounds ◽  
Aryl Halide ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Synthetic Organic Chemistry ◽  
Previous Review ◽  
Cross Coupling Reaction ◽  
Palladium Catalyzed

: The palladium-catalyzed reaction of aryl halide and boronic acid for the formation of C–C bonds so-called Suzuki–Miyaura cross-coupling reaction has many applications in Modern Synthetic Organic Chemistry. In 2013, we emphasized the applications of the intramolecular Suzuki cross-coupling reaction in cyclization and heterocyclization. Due to a plethora relevant papers appeared in the chemical literature, herein, we wish to cover by updating our previous review, the applications of the intramolecular Suzuki cross-coupling reaction in cyclization and heterocyclization leading to various homocyclic and heterocyclic compounds reported during a period of 2013 to 2018.

ChemInform Abstract: Palladium-Catalyzed Cross-Coupling Reaction of N-Alkoxyimidoyl Bromides and Its Application to One-Pot Synthesis of N-Arylamines.

ChemInform ◽  
2012 ◽  
Vol 43 (9) ◽  
pp. no-no
Author(s):  
Masafumi Ueda ◽  
Shoichi Sugita ◽  
Naoki Aoi ◽  
Aoi Sato ◽  
Yuki Ikeda ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
One Pot ◽  
One Pot Synthesis ◽  
Cross Coupling Reaction ◽  
Palladium Catalyzed

Palladium-catalyzed Suzuki cross-couplings of N′-mesyl arylhydrazines via C–N bond cleavage

RSC Advances ◽  
2014 ◽  
Vol 4 (49) ◽  
pp. 25576-25579 ◽  
Author(s):  
He-Ping Zhou ◽  
Jin-Biao Liu ◽  
Jian-Jun Yuan ◽  
Yi-Yuan Peng
Keyword(s):  
Boronic Acid ◽  
Bond Cleavage ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Mild Conditions ◽  
Cross Coupling Reaction ◽  
Palladium Catalyzed ◽  
High Yields ◽  
Aryl Boronic Acid ◽  
Biaryl Compounds

An efficient palladium-catalyzed Suzuki cross-coupling reaction of N′-mesyl arylhydrazine with aryl boronic acid is described, which affords the corresponding biaryl compounds in high yields. This transformation proceeds through C–N bond cleavage under mild conditions.

One-Pot Palladium-Catalyzed Cross-Coupling Reaction of Aryl Iodides with Stannylarsanes and Stannylstibanes

2003 ◽  
Vol 5 (15) ◽  
pp. 2731-2734 ◽  
Author(s):  
Mariana Bonaterra ◽  
Sandra E. Martín ◽  
Roberto A. Rossi
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
One Pot ◽  
Aryl Iodides ◽  
Cross Coupling Reaction ◽  
Palladium Catalyzed

One-pot synthesis of benzoxaborole derivatives from the palladium-catalyzed cross-coupling reaction of alkoxydiboron with unprotected o-bromobenzylalcohols

2015 ◽  
Vol 13 (46) ◽  
pp. 11362-11368 ◽  
Author(s):  
Jianan Zhu ◽  
Ying Wei ◽  
Dongqing Lin ◽  
Changjin Ou ◽  
Linghai Xie ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
One Pot ◽  
Mild Conditions ◽  
One Pot Synthesis ◽  
Cross Coupling Reaction ◽  
Palladium Catalyzed

Under very mild conditions, functionalized benzoxaborole derivatives were prepared in good to excellent yields via a palladium-catalyzed Miyaura borylation reaction of readily available unprotected o-bromobenzylalcohols, and bis(pinacolato)diboron (B2pin2) without the assistance of an acid.

scholarly journals 2′-Chloro-4-(1-methyl-1H-imidazol-2-yl)-2,4′-bipyridine

Molbank ◽  
10.3390/m1040 ◽  
2018 ◽  
Vol 2019 (1) ◽  
pp. M1040 ◽  
Author(s):  
Dhafer Zinad ◽  
Dunya AL-Duhaidahaw ◽  
Ahmed Al-Amiery
Keyword(s):  
Mass Spectrometry ◽  
Boronic Acid ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Gas Chromatography Mass Spectrometry ◽  
Target Compound ◽  
Chromatography Mass Spectrometry ◽  
Cross Coupling Reaction ◽  
Palladium Catalyzed ◽  
Layer Chromatography

The compound 2′-chloro-4-(1-methyl-1H-imidazol-2-yl)-2,4′-bipyridine was obtained with a good yield by the reaction of 2-chloro-4-(1-methyl-1H-imidazol-2-yl)pyridine with (2-chloropyridin-4-yl)boronic acid and structurally characterized by nuclear magnetic resonance (1H-NMR and 13C-NMR), thin-layer chromatography–mass spectrometry (TLC–MS), HPLC, gas chromatography–mass spectrometry (GC–MS), and elemental analysis. The functionalization of the pyridine was achieved by the palladium-catalyzed Suzuki–Miyaura carbon–carbon cross-coupling reaction that afforded the target compound.

2,3,2′,3′-Tetramethylbiphenyl

2006 ◽  
Vol 62 (5) ◽  
pp. o2012-o2013
Author(s):  
Wei Zheng ◽  
Hong-Jun Zhu ◽  
Yi Qian ◽  
Yi-Zu Wu
Keyword(s):  
Crystal Structure ◽  
Intermolecular Interactions ◽  
Title Compound ◽  
Boronic Acid ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Twofold Axis ◽  
Compound C ◽  
Cross Coupling Reaction ◽  
Palladium Catalyzed

The title compound, C16H18, was synthesized by a palladium-catalyzed boronic acid cross-coupling reaction. A crystallographic twofold axis passes through the mid-point of the C—C bond connecting the two rings. In the crystal structure, two fairly close C—H...π(arene) contacts appear to be the only significant intermolecular interactions.

ChemInform Abstract: Efficient Phosphine Ligands for the One-Pot Palladium-Catalyzed Borylation/Suzuki-Miyaura Cross-Coupling Reaction.

ChemInform ◽  
2015 ◽  
Vol 46 (28) ◽  
pp. no-no
Author(s):  
You Chen ◽  
Hui Peng ◽  
Yun-Xiao Pi ◽  
Tong Meng ◽  
Ze-Yu Lian ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
Phosphine Ligands ◽  
One Pot ◽  
Cross Coupling Reaction ◽  
Palladium Catalyzed ◽  
The One
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