Hydantoins are an important class of heterocycles with applications in pharmacy, agriculture, and as intermediates in organic synthesis. Traditional synthetic procedures to access hydantoins are target oriented with multiple synthetic steps, often use reagents that are not commercially available, and are not sustainable. Herein, an efficient process is described accessing hydantoins starting from commercially available amines using consecutive gas/liquid transformations (oxygen, carbon dioxide). This semi-continuous process produced ten benzylic/aliphatic hydantoins in good overall yields (52-84%)
2-Methyleneaziridines can be transformed into 5,5'-disubstituted hydantoins in moderate to good yiel...
Diversely substituted hydantoins have been synthesized by new strategy from cyanamide based precurso...
A series of hydantoins and thiohydantoins have been synthesized in water at room temperature from ur...
Hydantoins are an important class of heterocycles with applications in pharmacy, agriculture, and as...
The Bucherer-Bergs reaction is a classical multi-component reaction that yields hydantoins, which ca...
The development of new practical and green methods for the synthesis of small heterocycles is an at...
An efficient and straightforward two-step procedure for the synthesis of N-1 alkyl/aryl-substituted ...
Hydantoins and their hybrids with other molecules represent a very important group of heterocycles b...
A method for the synthesis of enantiopure 1,5-substituted hydantoins was developed using a hypervale...
A method for the synthesis of enantiopure 1,5-substituted hydantoins was developed using a hypervale...
A novel, three-component process for the preparation of a small library of unprecedented nonracemic ...
Continuous flow processing was applied for the rapid replacement of an aromatic amino group with a h...
Generally, synthesis of hydantoin derivatives involve use of carbonyl compounds which in turn requir...
The eco-friendly preparation of 5- and 5,5-disubstituted hydantoins from various amino ester hydroch...
The metalation of hydantoin and thiohydantoin has been conducted in liquid ammonia and then the reac...
2-Methyleneaziridines can be transformed into 5,5'-disubstituted hydantoins in moderate to good yiel...
Diversely substituted hydantoins have been synthesized by new strategy from cyanamide based precurso...
A series of hydantoins and thiohydantoins have been synthesized in water at room temperature from ur...
Hydantoins are an important class of heterocycles with applications in pharmacy, agriculture, and as...
The Bucherer-Bergs reaction is a classical multi-component reaction that yields hydantoins, which ca...
The development of new practical and green methods for the synthesis of small heterocycles is an at...
An efficient and straightforward two-step procedure for the synthesis of N-1 alkyl/aryl-substituted ...
Hydantoins and their hybrids with other molecules represent a very important group of heterocycles b...
A method for the synthesis of enantiopure 1,5-substituted hydantoins was developed using a hypervale...
A method for the synthesis of enantiopure 1,5-substituted hydantoins was developed using a hypervale...
A novel, three-component process for the preparation of a small library of unprecedented nonracemic ...
Continuous flow processing was applied for the rapid replacement of an aromatic amino group with a h...
Generally, synthesis of hydantoin derivatives involve use of carbonyl compounds which in turn requir...
The eco-friendly preparation of 5- and 5,5-disubstituted hydantoins from various amino ester hydroch...
The metalation of hydantoin and thiohydantoin has been conducted in liquid ammonia and then the reac...
2-Methyleneaziridines can be transformed into 5,5'-disubstituted hydantoins in moderate to good yiel...
Diversely substituted hydantoins have been synthesized by new strategy from cyanamide based precurso...
A series of hydantoins and thiohydantoins have been synthesized in water at room temperature from ur...