Add to ORKGUse of allylamine and substituted 2-furaldehydes as components in Ugi-Smiles couplings of 2-nitrophenol provide ready access to N-aryl epoxyisoindolines. These adducts form via a dual event involving the Ugi-Smiles multicomponent reaction and an intramolecular Diels-Alder cycloaddition with the furan ring
Ces travaux mettent en valeur les réactions multicomposants a base d'isonitriles dans différentes ap...
An efficient direct coupling procedure for the synthesis of N-acyl-2-oxazolidinones derived from alp...
The first chapter of this thesis consists of two related projects that explore novel reactivity of d...
A multicomponent coupling reaction (MCR) is a very efficient synthetic method, capable of forming se...
With the endeavor to find new efficient synthetic methods to rapidly access diverse molecular struct...
A multicomponent coupling reaction (MCR) is a highly efficient process that is capable of producing ...
Synthesis of complex, biologically active molecules is critical for the discovery and development of...
Organic methodology development is focused on finding new ways to prepare organic compounds. Multico...
Abstract Efficient one-pot Ugi-Smiles couplings are reported for the use of furyl-substituted aldehy...
Ugi type reactions are well known for decades. These multicomponent reactions involve an aldehyde,an...
A multicomponent coupling reaction (MCR) is a powerful transformation, combining three or more start...
International audienceA short sequential synthesis of pyrrolidino- pyridines and pyrimidines illustr...
Multicomponent coupling reactions (MCRs) are high-conversion, one-pot processes that combine three o...
We report here selective Tsuji-Trost type allylation of Ugi adducts using a strategy based on the en...
Les réactions de type Ugi sont connues depuis une cinquantaine d’années. Ces réactions multicomposan...
Ces travaux mettent en valeur les réactions multicomposants a base d'isonitriles dans différentes ap...
An efficient direct coupling procedure for the synthesis of N-acyl-2-oxazolidinones derived from alp...
The first chapter of this thesis consists of two related projects that explore novel reactivity of d...
A multicomponent coupling reaction (MCR) is a very efficient synthetic method, capable of forming se...
With the endeavor to find new efficient synthetic methods to rapidly access diverse molecular struct...
A multicomponent coupling reaction (MCR) is a highly efficient process that is capable of producing ...
Synthesis of complex, biologically active molecules is critical for the discovery and development of...
Organic methodology development is focused on finding new ways to prepare organic compounds. Multico...
Abstract Efficient one-pot Ugi-Smiles couplings are reported for the use of furyl-substituted aldehy...
Ugi type reactions are well known for decades. These multicomponent reactions involve an aldehyde,an...
A multicomponent coupling reaction (MCR) is a powerful transformation, combining three or more start...
International audienceA short sequential synthesis of pyrrolidino- pyridines and pyrimidines illustr...
Multicomponent coupling reactions (MCRs) are high-conversion, one-pot processes that combine three o...
We report here selective Tsuji-Trost type allylation of Ugi adducts using a strategy based on the en...
Les réactions de type Ugi sont connues depuis une cinquantaine d’années. Ces réactions multicomposan...
Ces travaux mettent en valeur les réactions multicomposants a base d'isonitriles dans différentes ap...
An efficient direct coupling procedure for the synthesis of N-acyl-2-oxazolidinones derived from alp...
The first chapter of this thesis consists of two related projects that explore novel reactivity of d...