Research progress is often promoted by unexpected results that open the way to new scenarios. In this communication, an unprecedented condensation of arylacetic acids and isocyanides and the unusual base-mediated rearrangement of the resulting products to give two novel classes of polysubstituted pyrrolones and pyrrolidinediones are reported
A new method for the synthesis of N-substituted isoindolinones and 3-arylaminophthalides was develop...
Several pyrrolidine-2,3-diones have been synthesised by condensation of oxalacetic ester and phenyl ...
The reaction of aryl acetylide anions with phenyl isocyanate and subsequent addition of a protonatin...
Research progress is often promoted by unexpected results that open the way to new scenarios. In thi...
Pyrroles are among the most privileged and influential small N-heterocycles at the core of many comm...
Old multicomponent reactions are still a source of inspiration for discovering novel combinations of...
A review. This account reviews the synthesis of functionalized isocyanides, including isocyanoacetat...
Isocyanide based multicomponent reactions, including the Ugi four-component and Passerini three-comp...
Enols are used for the first time in a condensation with aldehydes and isocyanides to selectively gi...
In continuation of our recent research on the development of novel multicomponent reactions with iso...
An efficient and practical method has been developed for the diversity-oriented synthesis of chromon...
Old multicomponent reactions are still a source of inspiration for discovering novel combinations of...
A route towards pyrrolo[2,1-a]isoquinolines through a 3CR of 1-aroyl dihydroisoquinolines, activated...
In this review, we update our previous presentation, underscoring the recent applications of isocyan...
A number of 2,3-pyrrolidinediones have been synthesised by the condensation of phenylpyruvic, 3,4-di...
A new method for the synthesis of N-substituted isoindolinones and 3-arylaminophthalides was develop...
Several pyrrolidine-2,3-diones have been synthesised by condensation of oxalacetic ester and phenyl ...
The reaction of aryl acetylide anions with phenyl isocyanate and subsequent addition of a protonatin...
Research progress is often promoted by unexpected results that open the way to new scenarios. In thi...
Pyrroles are among the most privileged and influential small N-heterocycles at the core of many comm...
Old multicomponent reactions are still a source of inspiration for discovering novel combinations of...
A review. This account reviews the synthesis of functionalized isocyanides, including isocyanoacetat...
Isocyanide based multicomponent reactions, including the Ugi four-component and Passerini three-comp...
Enols are used for the first time in a condensation with aldehydes and isocyanides to selectively gi...
In continuation of our recent research on the development of novel multicomponent reactions with iso...
An efficient and practical method has been developed for the diversity-oriented synthesis of chromon...
Old multicomponent reactions are still a source of inspiration for discovering novel combinations of...
A route towards pyrrolo[2,1-a]isoquinolines through a 3CR of 1-aroyl dihydroisoquinolines, activated...
In this review, we update our previous presentation, underscoring the recent applications of isocyan...
A number of 2,3-pyrrolidinediones have been synthesised by the condensation of phenylpyruvic, 3,4-di...
A new method for the synthesis of N-substituted isoindolinones and 3-arylaminophthalides was develop...
Several pyrrolidine-2,3-diones have been synthesised by condensation of oxalacetic ester and phenyl ...
The reaction of aryl acetylide anions with phenyl isocyanate and subsequent addition of a protonatin...