CH Activation Reactions of Ruthenium N-Heterocyclic Carbene Complexes:  Application in a Catalytic Tandem Reaction Involving CC Bond Formation from Alcohols

2007 ◽  
Vol 129 (7) ◽  
pp. 1987-1995 ◽  
Author(s):  
Suzanne Burling ◽  
Belinda M. Paine ◽  
Devendrababu Nama ◽  
Victoria S. Brown ◽  
Mary F. Mahon ◽  
...  
RSC Advances ◽  
2018 ◽  
Vol 8 (39) ◽  
pp. 22122-22126 ◽  
Author(s):  
Raveendra Jillella ◽  
Chang Ho Oh

Copper-catalyzed domino cyclization of 2-alkynylanilines followed by C–C bond formation with quinones is an efficient method of accessing 3-indolyl quinones.


ChemInform ◽  
2016 ◽  
Vol 47 (26) ◽  
Author(s):  
Yue Yu ◽  
Songjian Yi ◽  
Chuanle Zhu ◽  
Weigao Hu ◽  
Bingjie Gao ◽  
...  

2019 ◽  
Vol 55 (3) ◽  
pp. 217-228 ◽  
Author(s):  
Vladimir A. Glushkov ◽  
Michail S. Denisov ◽  
Aleksey A. Gorbunov ◽  
Yurii A. Myalitzin ◽  
Maksim V. Dmitriev ◽  
...  

2003 ◽  
Vol 75 (4) ◽  
pp. 435-443 ◽  
Author(s):  
Robert H. Crabtree

Routes to pincer and chelate carbene complexes of Pd, Rh, and Ir include double geminal CH activation, metallation, and CH activation. Abnormal binding via imidazole C5 can occur, and ion pairing can strongly influence C2 vs. C5 binding. Prior ligand binding via pyridine N before metallation is not essential. Computational methods are used extensively, for example, to compare N vs. C binding in imidazole. The possibility of C binding by histidine in metalloenzymes is discussed.


2016 ◽  
Vol 12 ◽  
pp. 81-88 ◽  
Author(s):  
Senem Akkoç ◽  
Yetkin Gök ◽  
İlhan Özer İlhan ◽  
Veysel Kayser

A series of novel benzimidazolium salts (1–4) and their pyridine enhanced precatalyst preparation stabilization and initiation (PEPPSI) themed palladium N-heterocyclic carbene complexes [PdCl2(NHC)(Py)] (5–8), where NHC = 1-(N-methylphthalimide)-3-alkylbenzimidazolin-2-ylidene and Py = 3-chloropyridine, were synthesized and characterized by means of 1H and 13C{1H} NMR, UV–vis (for 5–8), ESI-FTICR-MS (for 2, 4, 6–8) and FTIR spectroscopic methods and elemental analysis. The synthesized compounds were tested in Suzuki–Miyaura cross-coupling (for 1–8) and arylation (for 5–8) reactions. As catalysts, they demonstrated a highly efficient route for the formation of asymmetric biaryl compounds even though they were used in very low loading. For example, all compounds displayed good catalytic activity for the C–C bond formation of 4-tert-butylphenylboronic acid with 4-chlorotoluene.


2014 ◽  
Vol 20 (38) ◽  
pp. 12046-12050 ◽  
Author(s):  
Xian-Rong Song ◽  
Ya-Ping Han ◽  
Yi-Feng Qiu ◽  
Zi-Hang Qiu ◽  
Xue-Yuan Liu ◽  
...  

RSC Advances ◽  
2020 ◽  
Vol 10 (44) ◽  
pp. 26414-26417
Author(s):  
Rongrong Cai ◽  
Qicai Wei ◽  
Runsheng Xu

A nickel-catalyzed tandem reaction involving cyclic esterification/C–S bond formation has been developed.


2016 ◽  
Vol 18 (3) ◽  
pp. 400-403 ◽  
Author(s):  
Yue Yu ◽  
Songjian Yi ◽  
Chuanle Zhu ◽  
Weigao Hu ◽  
Bingjie Gao ◽  
...  

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