Journal
CATALYSIS LETTERS
Volume 147, Issue 5, Pages 1114-1126Publisher
SPRINGER
DOI: 10.1007/s10562-016-1957-5
Keywords
Suzuki; Heck; Stille; Cross coupling reactions; Mesoporous silica; Vanillin Palladium
Categories
Funding
- Ilam University, Ilam, Iran
Ask authors/readers for more resources
The present work describes the use of palladium-vanillin-Schiff-base complex immobilized on MCM-41 nanostructure as efficient catalyst for the Suzuki-Miyaura, Stille and Mizoroki-Heck reactions of several aryl halides under aerobic conditions. All the reactions were carried out in green solvents (H2O and PEG-400). The developed procedure results bring several benefits such as uses of inexpensive and non-toxic ligand (vanillin), easy catalyst/product separation and catalyst recycling. The catalyst can be reused at least for five consecutive cycles without a significant loss of its catalytic activity or metal leaching.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available