A K<sub>2</sub>S<sub>2</sub>O<sub>8</sub>/TEMPO-induced oxidative cyclization of <i>N</i>-unprotected enaminoesters and enaminones that gave 1<i>H</i>-pyrrol-2(3<i>H</i>)-ones in good yields with broad functional group compatibility is reported. This method provides easy access to 1,2-carbon migration of ester or acyl group under transition-metal-free conditions
Amide bond formation is one of the most important transformations in organic synthesis, drug develop...
A novel Cu(TFA)<sub>2</sub>-catalyzed oxidative tandem cyclization/1,2-alkyl migration of readily av...
3-Pyrroline reacts with cyclic ketones to form enamines as kinetically controlled products. Under mo...
A novel and efficient copper-catalyzed tandem oxidative cyclization/1,2-amino migration of readily a...
Tetrasubstituted pyrroles have been synthesized via the cross-dehydrogenative coupling between enami...
The palladium-catalyzed reaction of acetyl oximes with isocyanides was developed for the synthesis o...
A novel iodine promoted cyclization of enaminone with aryl methyl ketones has been developed as a st...
The palladium-catalyzed reaction of acetyl oximes with isocyanides was developed for the synthesis o...
The palladium-catalyzed reaction of acetyl oximes with isocyanides was developed for the synthesis o...
Pd-catalyzed cyclizations of oxime esters with 1,2-dialkylated alkenes provide an entry to chiral di...
A novel, transition metal-free and one-pot methodology to synthesize various substituted NH-pyrroles...
Pd-catalyzed cyclizations of oxime esters with 1,2-dialkylated alkenes provide an entry to chiral di...
© A one-pot two-step protocol for the synthesis of 2-acetyl-1H-pyrroles from N-propargylic β-enamino...
3-Pyrroline reacts with cyclic ketones to form enamines as kinetically controlled products. Under mo...
A novel Cu(TFA)<sub>2</sub>-catalyzed oxidative tandem cyclization/1,2-alkyl migration of readily av...
Amide bond formation is one of the most important transformations in organic synthesis, drug develop...
A novel Cu(TFA)<sub>2</sub>-catalyzed oxidative tandem cyclization/1,2-alkyl migration of readily av...
3-Pyrroline reacts with cyclic ketones to form enamines as kinetically controlled products. Under mo...
A novel and efficient copper-catalyzed tandem oxidative cyclization/1,2-amino migration of readily a...
Tetrasubstituted pyrroles have been synthesized via the cross-dehydrogenative coupling between enami...
The palladium-catalyzed reaction of acetyl oximes with isocyanides was developed for the synthesis o...
A novel iodine promoted cyclization of enaminone with aryl methyl ketones has been developed as a st...
The palladium-catalyzed reaction of acetyl oximes with isocyanides was developed for the synthesis o...
The palladium-catalyzed reaction of acetyl oximes with isocyanides was developed for the synthesis o...
Pd-catalyzed cyclizations of oxime esters with 1,2-dialkylated alkenes provide an entry to chiral di...
A novel, transition metal-free and one-pot methodology to synthesize various substituted NH-pyrroles...
Pd-catalyzed cyclizations of oxime esters with 1,2-dialkylated alkenes provide an entry to chiral di...
© A one-pot two-step protocol for the synthesis of 2-acetyl-1H-pyrroles from N-propargylic β-enamino...
3-Pyrroline reacts with cyclic ketones to form enamines as kinetically controlled products. Under mo...
A novel Cu(TFA)<sub>2</sub>-catalyzed oxidative tandem cyclization/1,2-alkyl migration of readily av...
Amide bond formation is one of the most important transformations in organic synthesis, drug develop...
A novel Cu(TFA)<sub>2</sub>-catalyzed oxidative tandem cyclization/1,2-alkyl migration of readily av...
3-Pyrroline reacts with cyclic ketones to form enamines as kinetically controlled products. Under mo...