Synthesis and characterization of trinuclear N-heterocyclic carbene–palladium(ii) complexes and their applications in the Suzuki–Miyaura cross-coupling reaction

RSC Advances ◽  
2016 ◽  
Vol 6 (103) ◽  
pp. 100690-100695 ◽  
Author(s):  
Tao Wang ◽  
Lantao Liu ◽  
Kai Xu ◽  
Huanping Xie ◽  
Hui Shen ◽  
...  

Five novel trinuclear N-heterocyclic carbene–palladium(ii) complexes 5a–e were conveniently synthesized in one step. The obtained palladium(ii) complexes were the effective catalyst precursors for the Suzuki–Miyaura coupling.

ACS Omega ◽  
2020 ◽  
Vol 5 (16) ◽  
pp. 9598-9604
Author(s):  
Junya Ishida ◽  
Masato Nakatsuji ◽  
Tatsuki Nagata ◽  
Hideya Kawasaki ◽  
Takeyuki Suzuki ◽  
...  

2015 ◽  
Vol 11 ◽  
pp. 951-956 ◽  
Author(s):  
Sandrina Oliveira ◽  
Dulce Belo ◽  
Isabel Cordeiro Santos ◽  
Sandra Rabaça ◽  
Manuel Almeida

A dissymmetric TTF-type electron donor, cyanobenzene-ethylenedithio-tetrathiafulvalene (CNB-EDT-TTF), was obtained in high yield, by a cross-coupling reaction with triethyl phosphite between 2-thioxobenzo[d][1,3]dithiole-5-carbonitrile and 5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-one. This new donor was characterized namely by single crystal X-ray diffraction, cyclic voltammetry, NMR, UV-visible and IR spectroscopy.


RSC Advances ◽  
2020 ◽  
Vol 10 (39) ◽  
pp. 23108-23120 ◽  
Author(s):  
Samim Sultana ◽  
Swapna Devi Mech ◽  
Farhaz Liaquat Hussain ◽  
Pallab Pahari ◽  
Geetika Borah ◽  
...  

Here we report the synthesis and characterization of graphene oxide anchored Pd–Cu bimetallic nanoparticles by bio reduction method and its application in Sonogashira cross-coupling reaction.


Molecules ◽  
2020 ◽  
Vol 25 (3) ◽  
pp. 684
Author(s):  
Yingpeng Liu ◽  
Thanh C. Ho ◽  
Mohammed Baradwan ◽  
Maria Pascual Lopez-Alberca ◽  
Christos Iliopoulos-Tsoutsouvas ◽  
...  

A new approach to synthesize cannabilactones using Suzuki cross-coupling reaction followed by one-step demethylation-cyclization is presented. The two key cannabilactone prototypes AM1710 and AM1714 were obtained selectively in high overall yields and in a lesser number of synthetic steps when compared to our earlier synthesis. The new approach expedited the synthesis of cannabilactone analogs with structural modifications at the four potential pharmacophoric regions.


Sign in / Sign up

Export Citation Format

Share Document