Regioselective rhodium-catalyzed intermolecular [2+2+2] cycloaddition of alkynes and isocyanates to form pyridones
-
Add time:08/12/2019 Source:sciencedirect.com
A highly regioselective rhodium-catalyzed intermolecular [2+2+2] cycloaddition of terminal alkynes with a variety of isocyanates to provide 2- and 4-pyridones has been developed. This reaction proceeds in good to excellent yields and overcomes the problem of dimerization and trimerization through the use of phosphoramidite ligands. A CO migration in the metallacycle is proposed to account for the formation of 4-pyridone.
We also recommend Trading Suppliers and Manufacturers of 2-METHOXY-5-TRIFLUOROMETHYLPHENYL ISOCYANATE (cas 16588-75-3). Pls Click Website Link as below: cas 16588-75-3 suppliers
Prev:Palladium-catalyzed annulation of alkynyl aryl ethers with isocyanates through o-C–H cleavage. Synthesis of solid-state emissive 2-methylidene-2H-1,4-benzoxazin-3(4H)-ones
Next:Copper(II) triflate-catalyzed and tosyl isocyanate-mediated three-step tandem synthesis of 9-arylfluorenes) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information


