A facile Pd-catalyzed methodology providing an efficient synthetic route to biologically relevant arylpiperazines under aerobic conditions is reported. Electron donating and sterically hindered aryl chlorides were aminated to afford yields up to 97%, with examples using piperazine as solvent, illustrating an ecofriendly, cost-effective synthesis of these privileged structures
4-Aminophthalazin-1(2H)-ones (APOs) are underexplored heterocyclic compounds with promising and dive...
Easily accessible N-tosylglycine allylamides have been converted into diversely functionalized piper...
A palladium-catalyzed one-pot synthesis of phthalazinones from 2-halomethyl benzoates, paraformaldeh...
Abstract: The palladium-catalyzed coupling of amines and aryl halides or aryl alcohol derivatives ha...
We report here a novel method for the modular synthesis of highly substituted piperazines and relate...
A simple and efficient one-pot three-component synthetic route to highly substituted and functionali...
Piperazine ranks within the top three most utilized N-heterocyclic moieties in FDA-approved small-mo...
A cascade, metal promoted transformations utilizing chloro allenylamide, primary amine and aryl iodi...
An efficient one-pot synthesis is described for the preparation of 1,4-disubstituted piperazine-2,5-...
A bulky, inexpensive and simple bidentate ligand 1,4-bis(2-hydroxy-3,5-di-tert-butylbenzyl)piperazin...
Given the widespread importance of piperazines as building blocks for the production of pharmaceutic...
The activity of pharmacologically active compounds can be increased by presenting a drug in a define...
Piperazine scaffolds are amongst the most extensively used backbones in medicinal chemistry and many...
The stereocontrolled synthesis of functionalized piperazines is of great interest to pharmaceutical ...
Piperazines are widely used as central elements in the construction of bioactive molecules. Herein, ...
4-Aminophthalazin-1(2H)-ones (APOs) are underexplored heterocyclic compounds with promising and dive...
Easily accessible N-tosylglycine allylamides have been converted into diversely functionalized piper...
A palladium-catalyzed one-pot synthesis of phthalazinones from 2-halomethyl benzoates, paraformaldeh...
Abstract: The palladium-catalyzed coupling of amines and aryl halides or aryl alcohol derivatives ha...
We report here a novel method for the modular synthesis of highly substituted piperazines and relate...
A simple and efficient one-pot three-component synthetic route to highly substituted and functionali...
Piperazine ranks within the top three most utilized N-heterocyclic moieties in FDA-approved small-mo...
A cascade, metal promoted transformations utilizing chloro allenylamide, primary amine and aryl iodi...
An efficient one-pot synthesis is described for the preparation of 1,4-disubstituted piperazine-2,5-...
A bulky, inexpensive and simple bidentate ligand 1,4-bis(2-hydroxy-3,5-di-tert-butylbenzyl)piperazin...
Given the widespread importance of piperazines as building blocks for the production of pharmaceutic...
The activity of pharmacologically active compounds can be increased by presenting a drug in a define...
Piperazine scaffolds are amongst the most extensively used backbones in medicinal chemistry and many...
The stereocontrolled synthesis of functionalized piperazines is of great interest to pharmaceutical ...
Piperazines are widely used as central elements in the construction of bioactive molecules. Herein, ...
4-Aminophthalazin-1(2H)-ones (APOs) are underexplored heterocyclic compounds with promising and dive...
Easily accessible N-tosylglycine allylamides have been converted into diversely functionalized piper...
A palladium-catalyzed one-pot synthesis of phthalazinones from 2-halomethyl benzoates, paraformaldeh...