Journal
RSC ADVANCES
Volume 7, Issue 17, Pages 10469-10478Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7ra01087g
Keywords
-
Categories
Funding
- NAWI Graz and Research Center Pharmaceutical Engineering (RCPE) for the ReactIR system
Ask authors/readers for more resources
The palladium-catalyzed deoxygenation of o-vinylnitrobenzenes employing carbon monoxide as a terminal reductant produces indoles in a continuous flow environment. The reaction proceeds with catalyst loadings of 1 to 2 mol% Pd(OAc)(2) in the presence of suitable ligands/additives and generates carbon dioxide as the only stoichiometric side-product. The reductive cyclization proceeds in a clean fashion with high initial reaction rates in the pressurized flow reactor, ultimately leading to deposition of catalytically inactive palladium(0) inside the channels of the flow device, allowing for an efficient catalyst recovery. A variety of o-vinylnitrobenzenes (o-nitrostilbenes and -styrenes) were converted to the corresponding indoles within 15 to 30 min at a reaction temperature of 140 degrees C to furnish products in good to excellent yields (10-20 bar CO pressure). Mechanistic aspects and the scope of the transformation are discussed.
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