1174-1176An efficient and convenient procedure involving microwave and ultrasound conditions for the synthesis of 5,5-disubstituted hydantoins is reported. The combined use of microwave and ultrasound reduces the reaction time significantly. In the presence of potassium cyanide and ammonium carbonate, the acetyl ester bond is hydrolysed under both ultrasonic and reflux conditions
International audienceIn this laboratory classroom, students will be introduced to the three-step sy...
An efficient chemoselective hydrogenation protocol for substituted cinnamic esters is developed for ...
In the present investigation two amides were synthesized: N, N-diisopropiletanoamida and N, N-dibuty...
The rapid and highly ecient synthesis of hydantoin derivatives 3(a-f) was achieved under microwave i...
Monothiohydantoin 3a is made in seven steps front 1,4-diiodobenzene and is shown to be an inhibitor ...
2-(Alkyl-1-yl)-1H-imidazol-5(4H)-ones 5a–n were synthesized via nucleophilic substitution of the met...
The Bucherer-Bergs reaction is a classical multi-component reaction that yields hydantoins, which ca...
The present paper describes studies on the synthesis of the antiepileptic drug phenytoin, and of str...
A simple and efficient method for the synthesis of 7,8-diaminopelargonic acid, a key intermediate in...
A simple and efficient method for the synthesis of 7,8-diaminopelargonic acid, a key intermediate in...
1084-1087Ten new fluorine containing 1, 5-disubstituted hydantoins/thiohydantoi- ns 3 have been s...
Microwave-activated synthesis is a special and remarkable technique in modern synthetic organic chem...
A microwave-assisted mild protocol is developed for the synthesis of 5-isobutyl-3-methyl-4,5-dihydro...
An efficient synthesis of a methyl derivative of the indoloquinoline alkaloid cryptosanguinolentine ...
155-158The first total synthesis of two novel iso-branched heptadecenoic acids, the major components...
International audienceIn this laboratory classroom, students will be introduced to the three-step sy...
An efficient chemoselective hydrogenation protocol for substituted cinnamic esters is developed for ...
In the present investigation two amides were synthesized: N, N-diisopropiletanoamida and N, N-dibuty...
The rapid and highly ecient synthesis of hydantoin derivatives 3(a-f) was achieved under microwave i...
Monothiohydantoin 3a is made in seven steps front 1,4-diiodobenzene and is shown to be an inhibitor ...
2-(Alkyl-1-yl)-1H-imidazol-5(4H)-ones 5a–n were synthesized via nucleophilic substitution of the met...
The Bucherer-Bergs reaction is a classical multi-component reaction that yields hydantoins, which ca...
The present paper describes studies on the synthesis of the antiepileptic drug phenytoin, and of str...
A simple and efficient method for the synthesis of 7,8-diaminopelargonic acid, a key intermediate in...
A simple and efficient method for the synthesis of 7,8-diaminopelargonic acid, a key intermediate in...
1084-1087Ten new fluorine containing 1, 5-disubstituted hydantoins/thiohydantoi- ns 3 have been s...
Microwave-activated synthesis is a special and remarkable technique in modern synthetic organic chem...
A microwave-assisted mild protocol is developed for the synthesis of 5-isobutyl-3-methyl-4,5-dihydro...
An efficient synthesis of a methyl derivative of the indoloquinoline alkaloid cryptosanguinolentine ...
155-158The first total synthesis of two novel iso-branched heptadecenoic acids, the major components...
International audienceIn this laboratory classroom, students will be introduced to the three-step sy...
An efficient chemoselective hydrogenation protocol for substituted cinnamic esters is developed for ...
In the present investigation two amides were synthesized: N, N-diisopropiletanoamida and N, N-dibuty...
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