Indium tribromide catalyzes efficiently the aminolysis of activated aziridines with aromatic amines under mild reaction conditions to afford the corresponding vicinal-diamines in high yields with high selectivity
Indium(III) bromide has been used for the first time for the synthesis of propargyl amines in a one-...
Intramolecular aziridination remains a novel method for the creation of three-membered heterocyclic ...
We have developed a new synthetic method for the synthesis of aziridines using Chloramine-T as an ef...
An efficient catalytic method for the synthesis of alpha,beta-diamino acid derivatives has been deve...
Chiral allylic amines are synthesized in high yields by treatment of 2-iodomethyl N-tosyl aziridines...
A variety of N-tosyl aziridines undergo ring opening with indium trihalides in acetonitrile at ambie...
Pyrrole reacts smoothly with terminal epoxides in the presence of a catalytic amount of InBr<SUB>3</...
A variety of N-tosylaziridines undergo ring opening with pyrrole, furan, thiophene and indole in the...
The reaction of N-tert-butanesulfinyl imines 1 with 1,3-dibromopropene (2), in the presence of indiu...
An environmentally benign H<sub>3</sub>PMo<sub>12</sub>O<sub>40</sub>-SiO<sub>2</sub>-catalyzed regi...
Aziridines react smoothly with arenes in the presence of a catalytic amount of indium triflate at am...
Aziridinium ions are valuable reactive intermediates in organic synthesis. Regioselective and stereo...
750-753A strategy for achieving synthesis of aziridine employing iodine catalysed aziridination of ...
While methyl- and benzylamines opened N-tosyl aziridines 1 very efficiently in acetonitrile with com...
A simple and general method has been developed for the synthesis of α -aminonitriles by a one-pot th...
Indium(III) bromide has been used for the first time for the synthesis of propargyl amines in a one-...
Intramolecular aziridination remains a novel method for the creation of three-membered heterocyclic ...
We have developed a new synthetic method for the synthesis of aziridines using Chloramine-T as an ef...
An efficient catalytic method for the synthesis of alpha,beta-diamino acid derivatives has been deve...
Chiral allylic amines are synthesized in high yields by treatment of 2-iodomethyl N-tosyl aziridines...
A variety of N-tosyl aziridines undergo ring opening with indium trihalides in acetonitrile at ambie...
Pyrrole reacts smoothly with terminal epoxides in the presence of a catalytic amount of InBr<SUB>3</...
A variety of N-tosylaziridines undergo ring opening with pyrrole, furan, thiophene and indole in the...
The reaction of N-tert-butanesulfinyl imines 1 with 1,3-dibromopropene (2), in the presence of indiu...
An environmentally benign H<sub>3</sub>PMo<sub>12</sub>O<sub>40</sub>-SiO<sub>2</sub>-catalyzed regi...
Aziridines react smoothly with arenes in the presence of a catalytic amount of indium triflate at am...
Aziridinium ions are valuable reactive intermediates in organic synthesis. Regioselective and stereo...
750-753A strategy for achieving synthesis of aziridine employing iodine catalysed aziridination of ...
While methyl- and benzylamines opened N-tosyl aziridines 1 very efficiently in acetonitrile with com...
A simple and general method has been developed for the synthesis of α -aminonitriles by a one-pot th...
Indium(III) bromide has been used for the first time for the synthesis of propargyl amines in a one-...
Intramolecular aziridination remains a novel method for the creation of three-membered heterocyclic ...
We have developed a new synthetic method for the synthesis of aziridines using Chloramine-T as an ef...
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