Home Chemistry Heterocyclic Building Blocks Pyrrolidines Tert-Butyl 3-((Methylsulfonyl)Oxy)Pyrrolidine-1-Carboxylate
Substitution Reactions: The tert-butyl group 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 carbonyl group of the carboxylate can be reduced to the corresponding alcohol under appropriate conditions.
Oxidation: The methylsulfonyl group can undergo oxidation reactions under suitable conditions.
Ester Hydrolysis: Under acidic or basic conditions, the ester group can undergo hydrolysis to form the corresponding carboxylic acids and alcohols.
Decarboxylation: Under certain conditions, such as heating or treatment with specific reagents, decarboxylation may occur, leading to the loss of the carboxyl group and formation of the corresponding alkylamine.
Esterification: The carboxylate group can react with alcohols to form esters through esterification reactions.
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tert-Butyl 3-((methylsulfonyl)oxy)pyrrolidine-1-carboxylate
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(3R,4R)-tert-Butyl 3,4-bis((methylsulfonyl)oxy)pyrrolidine-1-carboxylate
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(R)-tert-Butyl 3-((methylsulfonyl)oxy)pyrrolidine-1-carboxylate
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(S)-tert-Butyl 3-((methylsulfonyl)oxy)pyrrolidine-1-carboxylate
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(2S,4R)-1-tert-Butyl 2-methyl 4-((methylsulfonyl)oxy)pyrrolidine-1,2-dicarboxylate
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