A wide variety of epoxides and aziridines were converted to the corresponding β-halohydrins and β-haloamines using cerium(III) chloride and the cerium(III) chloride/NaI system in acetonitrile. The reactions were highly regioselective and efficient with excellent yields under mild and neutral reaction conditions
The ring-opening reactions of 2-alkyl-substituted 1,1-bis(arylmethyl)- and 1-methyl-1-(1-phenylethyl...
Pyrrole reacts smoothly with terminal epoxides in the presence of a catalytic amount of InBr<SUB>3</...
Most nucleophilic aziridine ring opening reactions suffer from poor regio- and stereoselectivity. A ...
A wide variety of epoxides and aziridines were converted to the corresponding β-halohydrins and β-ha...
A wide variety of aziridines were converted to the corresponding β-haloamines using activated DMF co...
A variety of N-tosyl aziridines undergo ring opening with indium trihalides in acetonitrile at ambie...
We found that elemental iodine and bromine are converted to trihalide nucleophiles (triiodine and tr...
The first catalytic regioselective and stereospecific halogenation of 2,3-epoxy alcohols and 2,3-epo...
While methyl- and benzylamines opened N-tosyl aziridines 1 very efficiently in acetonitrile with com...
We report here the use of PPh3/halogenating agents as highly efficient reagents for the ring opening...
Aziridines react smoothly with sodium azide and sodium cyanide in the presence of catalytic amount o...
The regioselective opening of epoxides with organotin oxides 1 and 2, in presence of halogenated alc...
A new metal-free method is reported for the stereocontrolled opening of vinyl epoxides using boron t...
A wide variety of epoxides and aziridines were converted to the corresponding β-azido alcohols ...
We have developed a new synthetic method for the synthesis of aziridines using Chloramine-T as an ef...
The ring-opening reactions of 2-alkyl-substituted 1,1-bis(arylmethyl)- and 1-methyl-1-(1-phenylethyl...
Pyrrole reacts smoothly with terminal epoxides in the presence of a catalytic amount of InBr<SUB>3</...
Most nucleophilic aziridine ring opening reactions suffer from poor regio- and stereoselectivity. A ...
A wide variety of epoxides and aziridines were converted to the corresponding β-halohydrins and β-ha...
A wide variety of aziridines were converted to the corresponding β-haloamines using activated DMF co...
A variety of N-tosyl aziridines undergo ring opening with indium trihalides in acetonitrile at ambie...
We found that elemental iodine and bromine are converted to trihalide nucleophiles (triiodine and tr...
The first catalytic regioselective and stereospecific halogenation of 2,3-epoxy alcohols and 2,3-epo...
While methyl- and benzylamines opened N-tosyl aziridines 1 very efficiently in acetonitrile with com...
We report here the use of PPh3/halogenating agents as highly efficient reagents for the ring opening...
Aziridines react smoothly with sodium azide and sodium cyanide in the presence of catalytic amount o...
The regioselective opening of epoxides with organotin oxides 1 and 2, in presence of halogenated alc...
A new metal-free method is reported for the stereocontrolled opening of vinyl epoxides using boron t...
A wide variety of epoxides and aziridines were converted to the corresponding β-azido alcohols ...
We have developed a new synthetic method for the synthesis of aziridines using Chloramine-T as an ef...
The ring-opening reactions of 2-alkyl-substituted 1,1-bis(arylmethyl)- and 1-methyl-1-(1-phenylethyl...
Pyrrole reacts smoothly with terminal epoxides in the presence of a catalytic amount of InBr<SUB>3</...
Most nucleophilic aziridine ring opening reactions suffer from poor regio- and stereoselectivity. A ...
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