Home Chemistry Heterocyclic building blocks Pyrrolidines Proline
Nucleophilic Addition: Proline's pyrrolidine ring can undergo nucleophilic addition reactions at the carbonyl group, forming a tetrahedral intermediate.
Decarboxylation: Proline can undergo decarboxylation under certain conditions, leading to the formation of pyrrolidine.
Amidation: The carboxylic acid group of proline can react with amines to form amides.
Oxidation: Proline can be oxidized to form pyrrole-2-carboxylic acid under oxidative conditions.
Reduction: Proline can be reduced to form pyrrolidine under appropriate conditions.
Alkylation: The nitrogen atom in the pyrrolidine ring can be alkylated by reaction with alkyl halides or sulfonates.
Ring-closing Reactions: Proline can undergo ring-closing reactions to form cyclic compounds.
Substitution Reactions: Proline can undergo substitution reactions, such as nucleophilic substitution or electrophilic substitution.
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(2S,4S)-4-((tert-Butoxycarbonyl)amino)pyrrolidine-2-carboxylic acid
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(2S,4R)-1-(tert-Butoxycarbonyl)-4-((tert-butyldimethylsilyl)oxy)pyrrolidine-2-carboxylic acid
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rel-(2S,4R)-1-(tert-Butoxycarbonyl)-4-fluoropyrrolidine-2-carboxylic acid
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(2R,4S)-4-((tert-Butoxycarbonyl)amino)pyrrolidine-2-carboxylic acid
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(2S,4S)-1-(tert-Butoxycarbonyl)-4-(difluoromethyl)pyrrolidine-2-carboxylic acid
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