Journal
MONATSHEFTE FUR CHEMIE
Volume 143, Issue 5, Pages 791-795Publisher
SPRINGER WIEN
DOI: 10.1007/s00706-011-0632-1
Keywords
Catalyst; Arylation; Transition metals compounds; Silicates
Categories
Funding
- Islamic Azad University, Kazerun Branch, Iran
- Islamic Azad University, Fasa
- Khorasgan Branches, Iran
Ask authors/readers for more resources
Aryldiazonium silica sulfates were employed as new and efficient reagents for Heck-type arylation reactions with styrene and methyl acrylate. The reactions were carried out in an organic solvent, in the presence of Pd(OAc)(2) as precatalyst without use of base and free ligand. The trans isomers of desired products, methyl cinnamates and stilbenes, were obtained with full conversion. Use of a catalytic amount of Pd(OAc)(2) produced the corresponding products in short reaction times and excellent yields.
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