ChemInform Abstract: A Palladium-Catalyzed Domino Reaction of 3-Acetyl-5-hexyn-2-one with Aryl Iodides under Carbon Monoxide.

ChemInform ◽  
2010 ◽  
Vol 27 (51) ◽  
pp. no-no
Author(s):  
A. ARCADI ◽  
E. ROSSI
ChemInform ◽  
2003 ◽  
Vol 34 (24) ◽  
Author(s):  
Sandro Cacchi ◽  
Giancarlo Fabrizi ◽  
Federica Gavazza ◽  
Antonella Goggiamani

2016 ◽  
Vol 2016 (34) ◽  
pp. 5616-5619 ◽  
Author(s):  
Hai-Yu He ◽  
Wei Wang ◽  
Xiao-Jun Yu ◽  
Jin Huang ◽  
Lei Jian ◽  
...  

Synthesis ◽  
2019 ◽  
Vol 52 (04) ◽  
pp. 581-590 ◽  
Author(s):  
Zhaotao Xu ◽  
Bin Huang ◽  
Zebiao Zhou ◽  
Mingzhong Cai

A highly efficient and practical heterogeneous palladium-catalyzed carbonylative coupling of 2-iodoanilines with aryl iodides has been developed. The reaction occurs smoothly in toluene at 110 °C with N,N-diisopropylethylamine as base under carbon monoxide (5 bar) and offers a general and powerful tool for the construction of various valuable 2-arylbenzoxazinones with excellent atom-economy, high functional group tolerance, good to high yields, and easy recyclability of the palladium catalyst. The reaction is the first example of heterogeneous palladium-catalyzed carbonylative coupling for the preparation of diverse 2-arylbenzoxazinones from commercially easily available 2-iodoanilines and aryl iodides.


2017 ◽  
Vol 8 (2) ◽  
pp. 1002-1007 ◽  
Author(s):  
Jevgenijs Tjutrins ◽  
Bruce A. Arndtsen

We describe here a tandem catalytic route to prepare imidazoles in a single operation from aryl iodides, imines and CO.


2003 ◽  
Vol 5 (3) ◽  
pp. 289-291 ◽  
Author(s):  
Sandro Cacchi ◽  
Giancarlo Fabrizi ◽  
Federica Gavazza ◽  
Antonella Goggiamani

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