Step‐by‐step synthesis of copper(I) complex supported on platinum nanoparticle‐decorated mesoporous silica hollow spheres and its remarkable catalytic performance in Sonogashira coupling reaction

2020 ◽  
Vol 34 (7) ◽  
Author(s):  
Abdolghafar Abolhosseini Shahrnoy ◽  
Ali Reza Mahjoub ◽  
Sudabeh Shokrollahi ◽  
Nasim Ezzati ◽  
Kristiane Elsner ◽  
...  
Keyword(s):  
Mesoporous Silica ◽  
Hollow Spheres ◽  
Coupling Reaction ◽  
Catalytic Performance ◽  
Sonogashira Coupling ◽  
Platinum Nanoparticle ◽  
Sonogashira Coupling Reaction

Facile and surfactant-free synthesis of Pd nanoparticles by the extract of the fruits of Piper longum and their catalytic performance for the Sonogashira coupling reaction in water under ligand- and copper-free conditions

RSC Advances ◽  
2015 ◽  
Vol 5 (4) ◽  
pp. 2562-2567 ◽  
Author(s):  
Mahmoud Nasrollahzadeh ◽  
S. Mohammad Sajadi ◽  
Mehdi Maham ◽  
Ali Ehsani
Keyword(s):  
Palladium Nanoparticles ◽  
Coupling Reaction ◽  
Pd Nanoparticles ◽  
Catalytic Performance ◽  
Sonogashira Coupling ◽  
Facile Synthesis ◽  
Piper Longum ◽  
Sonogashira Coupling Reaction ◽  
Reaction In Water

This work reports a facile synthesis of palladium nanoparticles (Pd NPs) by the extract of the fruits of Piper longum without any stabilizer or surfactant.

ChemInform Abstract: 2,5-Bis(2-(diphenylphosphino)phenyl)-1,3,4-oxadiazole Ligands and Their Cu(I) Complexes for Sonogashira Coupling Reaction.

ChemInform ◽  
2014 ◽  
Vol 45 (35) ◽  
pp. no-no
Author(s):  
Cai-Xia Lin ◽  
Jia-Fang Zhu ◽  
Qing-Shan Li ◽  
Li-Hua Ao ◽  
Yan-Juan Jin ◽  
...  
Keyword(s):  
Coupling Reaction ◽  
Sonogashira Coupling ◽  
Sonogashira Coupling Reaction

scholarly journals The Utility of Sonogashira Coupling Reaction for the Derivatization of Aryl Halides with Fluorescent Alkyne

2018 ◽  
Vol 34 (10) ◽  
pp. 1183-1188 ◽  
Author(s):  
Naoyuki YASAKA ◽  
Naoya KISHIKAWA ◽  
Takumi HIGASHIJIMA ◽  
Kaname OHYAMA ◽  
Naotaka KURODA
Keyword(s):  
Coupling Reaction ◽  
Aryl Halides ◽  
Sonogashira Coupling ◽  
Sonogashira Coupling Reaction

scholarly journals Synthesis of 9-arylalkynyl- and 9-aryl-substituted benzo[b]quinolizinium derivatives by Palladium-mediated cross-coupling reactions

2018 ◽  
Vol 14 ◽  
pp. 1871-1884 ◽  
Author(s):  
Siva Sankar Murthy Bandaru ◽  
Darinka Dzubiel ◽  
Heiko Ihmels ◽  
Mohebodin Karbasiyoun ◽  
Mohamed M A Mahmoud ◽  
...  
Keyword(s):  
Emission Intensity ◽  
Binding Constants ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Coupling Reactions ◽  
Sonogashira Coupling ◽  
Reaction Conditions ◽  
Quadruplex Dna ◽  
Cross Coupling Reactions ◽  
Sonogashira Coupling Reaction

9-Arylbenzo[b]quinolizinium derivatives were prepared with base-free Suzuki–Miyaura coupling reactions between benzo[b]quinolizinium-9-trifluoroborate and selected benzenediazonium salts. In addition, the Sonogashira coupling reaction between 9-iodobenzo[b]quinolizinium and the arylalkyne derivatives yielded four novel 9-(arylethynyl)benzo[b]quinolizinium derivatives under relatively mild reaction conditions. The 9-(N,N-dimethylaminophenylethynyl)benzo[b]quinolizinium is only very weakly emitting, but the emission intensity increases by a factor >200 upon protonation, so that this derivative may operate as pH-sensitive light-up probe. Photometric and fluorimetric titrations of duplex and quadruplex DNA to 9-(arylethynyl)benzo[b]quinolizinium derivatives revealed a significant binding affinity of these compounds towards both DNA forms with binding constants ofKb= 0.2–2.2 × 105M−1.

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