Home Chemistry Heterocyclic Building Blocks Pyrrolidines Pyrrolidin-3-Ol
Esterification: Reaction with a carboxylic acid or acid derivative can lead to the formation of an ester.
Acylation: The nitrogen atom in the pyrrolidine ring can undergo acylation reactions to form an amide.
Reduction: The carbonyl group in the pyrrolidin-3-ol can be reduced to a hydroxyl group.
Oxidation: The alcohol group can be oxidized to form an aldehyde or a carboxylic acid .
Alkylation: The nitrogen atom can be alkylated by reaction with alkyl halides or sulfonates.
Substitution Reactions: The nitrogen atom can undergo substitution reactions, such as nucleophilic substitution.
Condensation Reactions: It can participate in condensation reactions to form cyclic compounds or larger molecules.
Ring-opening Reactions: The pyrrolidine ring can undergo ring-opening reactions under certain conditions.
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tert-Butyl ((3R,4R)-4-hydroxypyrrolidin-3-yl)carbamate hydrochloride
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(3R,4S)-1-Boc-3-fluoro-4-hydroxypyrrolidine
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(2S,4R)-4-Hydroxypyrrolidine-2-carboxylic acid hydrochloride
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1-(tert-Butoxycarbonyl)-4-hydroxy-3-methylpyrrolidine-3-carboxylic acid
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tert-Butyl 2-ethyl-4-hydroxypyrrolidine-1-carboxylate
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trans-tert-Butyl 3-fluoro-4-hydroxypyrrolidine-1-carboxylate
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tert-Butyl (3S,4R)-3-fluoro-4-hydroxypyrrolidine-1-carboxylate
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