Home Chemistry Heterocyclic Building Blocks Pyrrolidines 2,2-Dimethylpyrrolidine
Substitution Reactions: The nitrogen atom can undergo substitution reactions, such as nucleophilic substitution or electrophilic substitution.
Ring-opening Reactions: The pyrrolidine ring may undergo ring-opening reactions under certain conditions, leading to the formation of linear or branched compounds.
Reduction: The imine group can be reduced to form the corresponding amine.
Condensation Reactions: It can participate in condensation reactions to form cyclic compounds or larger molecules.
Oxidation: The amine groups can be oxidized to form the corresponding imine or iminium ion.
Hydrolysis: Under acidic or basic conditions, amide bonds can undergo hydrolysis to regenerate the amines and carboxylic acids.
Fragmentation: Under certain conditions, the pyrrolidine ring may undergo fragmentation reactions leading to the formation of smaller molecules.
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1-(tert-Butoxycarbonyl)-5,5-dimethylpyrrolidine-3-carboxylic acid
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