Paal-Knorr synthesis

Definition: The cyclisation of a 1,4-dicarbonyl compound with another molecule to give a five-membered aromatic ring compound.

ID: RXNO:0000161

More about the RSC Name Reaction Ontology (RXNO)

Articles referencing this term

Rhodium-catalysed hydroacylation or reductive aldol reactions: a ligand dependent switch of reactivity
James D. Osborne and Michael C. Willis, Chem. Commun., 2008 , 5025
DOI: 10.1039/b810935d

Magnetic nanoparticle-supported glutathione: a conceptually sustainable organocatalyst
Vivek Polshettiwar, Babita Baruwati and Rajender S. Varma, Chem. Commun., 2009 , 1837
DOI: 10.1039/b900784a

Domino allylic amination/Sonogashira/heterocyclisation reactions: palladium-catalysed three-component synthesis of pyrroles
Sandrine Lamandé-Langle, Mohamed Abarbri, Jérôme Thibonnet, Alain Duchêne and Jean-Luc Parrain, Chem. Commun., 2010 , 46 , 5157
DOI: 10.1039/c0cc00500b

Magnetically separable nanoferrite-anchored glutathione: aqueous homocoupling of arylboronic acids under microwave irradiation
Rafael Luque, Babita Baruwati and Rajender S. Varma, Green Chem., 2010 , 12 , 1540
DOI: 10.1039/c0gc00083c