A Rh-catalyzed enol-directed formal sp<sup>3</sup> C–H activation/annulation of α-arylidene pyrazolones with alkynes has been developed. This reaction provides a convenient route to synthesize spiropentadiene pyrazolones in good to excellent yields at room temperature, exhibiting good functional group tolerance, gram scalability, and high regioselectivity. Of note, the α-arylidene pyrazolone was introduced as a novel C3 synthon in C–H activation/annulation
Diastereoisomeric pyrazolone-fused spirocyclohexenimines, bearing contiguous all-carbon quaternary a...
Some marine shellfish toxins in the spiroimine family like gymnodimine and spirolides are produced b...
A novel consecutive three-component synthesis of 3-(hetero)aryl-1H-pyrazoles via room temperature So...
An effective diastereoselective Michael/alkylation cascade reaction of arylidenepyrazolones with 3-c...
Appropriately substituted 2-alkenylphenols undergo a mild formal [3C+2C] cycloaddition with alkyne...
Appropriately substituted 2-alkenylphenols undergo a mild formal [3C+2C] cycloaddition with alkyne...
An effective diastereoselective Michael/alkylation cascade reaction of arylidenepyrazolones with 3-c...
A palladium-catalyzed oxidative carbonylation of arylhydrazines and alkynes with balloon pressure CO...
Presented herein is a controllable selective construction of spiro or fused heterocyclic scaffolds t...
partially_open3noThis research was supported by MIUR, University of Salerno, POR Regione Campania FE...
Rh(III) catalyzed oxidative synthesis of pyrazoles from azomethines and acrylamide
Some marine shellfish toxins in the spiroimine family like gymnodimine and spirolides are produced b...
Bridged cycles are an important class of structural motif in various biologically active molecules. ...
Some marine shellfish toxins in the spiroimine family like gymnodimine and spirolides are produced b...
Diastereoisomeric pyrazolone-fused spirocyclohexenimines, bearing contiguous all-carbon quaternary a...
Diastereoisomeric pyrazolone-fused spirocyclohexenimines, bearing contiguous all-carbon quaternary a...
Some marine shellfish toxins in the spiroimine family like gymnodimine and spirolides are produced b...
A novel consecutive three-component synthesis of 3-(hetero)aryl-1H-pyrazoles via room temperature So...
An effective diastereoselective Michael/alkylation cascade reaction of arylidenepyrazolones with 3-c...
Appropriately substituted 2-alkenylphenols undergo a mild formal [3C+2C] cycloaddition with alkyne...
Appropriately substituted 2-alkenylphenols undergo a mild formal [3C+2C] cycloaddition with alkyne...
An effective diastereoselective Michael/alkylation cascade reaction of arylidenepyrazolones with 3-c...
A palladium-catalyzed oxidative carbonylation of arylhydrazines and alkynes with balloon pressure CO...
Presented herein is a controllable selective construction of spiro or fused heterocyclic scaffolds t...
partially_open3noThis research was supported by MIUR, University of Salerno, POR Regione Campania FE...
Rh(III) catalyzed oxidative synthesis of pyrazoles from azomethines and acrylamide
Some marine shellfish toxins in the spiroimine family like gymnodimine and spirolides are produced b...
Bridged cycles are an important class of structural motif in various biologically active molecules. ...
Some marine shellfish toxins in the spiroimine family like gymnodimine and spirolides are produced b...
Diastereoisomeric pyrazolone-fused spirocyclohexenimines, bearing contiguous all-carbon quaternary a...
Diastereoisomeric pyrazolone-fused spirocyclohexenimines, bearing contiguous all-carbon quaternary a...
Some marine shellfish toxins in the spiroimine family like gymnodimine and spirolides are produced b...
A novel consecutive three-component synthesis of 3-(hetero)aryl-1H-pyrazoles via room temperature So...