Home Chemistry Organic Building Blocks Amines Aziridine
Reduction:Reduction of aziridines with reducing agents such as lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4) can lead to the formation of primary amines.
Electrophilic Addition:Aziridines can undergo electrophilic addition reactions with electrophiles, such as halogens or electrophilic reagents, to form substituted aziridines.
Nitrogen Insertion:Aziridines can react with nitrogen-containing compounds, such as azides, to undergo nitrogen insertion reactions, leading to the formation of more complex nitrogen-containing compounds.
Cyclization:Aziridines can participate in intramolecular reactions, leading to the formation of cyclic compounds.
Functional Group Transformations:Aziridines can serve as intermediates in the synthesis of various other nitrogen-containing functional groups through further reactions, such as ring opening and subsequent modifications.
Metal-Catalyzed Reactions:Transition metal-catalyzed reactions, such as aziridination reactions using diazo compounds, can be employed to functionalize the aziridine ring.
Rearrangement Reactions:Aziridines can undergo rearrangement reactions, leading to the formation of different cyclic or acyclic compounds, depending on the reaction conditions.
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Lithium (R)-1-(tert-butoxycarbonyl)aziridine-2-carboxylate
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1-tert-Butyl 2-methyl aziridine-1,2-dicarboxylate
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tert-Butyl 2-methylaziridine-1-carboxylate
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(R)-1-tert-Butyl 2-methyl aziridine-1,2-dicarboxylate
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(S)-tert-Butyl 2-methylaziridine-1-carboxylate
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Lithium (S)-1-(tert-butoxycarbonyl)aziridine-2-carboxylate
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1-(tert-Butyl) 2-methyl (S)-aziridine-1,2-dicarboxylate
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(R)-tert-Butyl 2-methylaziridine-1-carboxylate
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