Home Chemistry Organic Building Blocks Amides Tert-Butyl-Cyclopent-2-En-1-Ylcarbamate
Ester Hydrolysis: The carbamate functional group (CONH-) can potentially undergo hydrolysis reactions under acidic or basic conditions, leading to the formation of a carboxylic acid and anamine.
Nucleophilic Addition: The carbamate nitrogen can act as a nucleophile and react with electrophiles, such as alkyl halides or other electrophilic species.
Esterification: The carbamate functional group may participate in esterification reactions with alcohols under appropriate conditions.
Cycloaddition Reactions: The cyclopentene ring may be involved in cycloaddition reactions, such as Diels-Alder reactions, with suitable dienophiles.
Oxidation Reactions: The tertiary butyl group may be susceptible to oxidation under certain conditions, potentially leading to the formation of a ketone or other oxidized products.
Elimination Reactions: The presence of a cyclopentene ring suggests the possibility of elimination reactions, especially under acidic or basic conditions.
Reductive Amination: Depending on the reaction conditions, the carbamate nitrogen might participate in reductive amination reactions with appropriate carbonyl compounds
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(1R,4R)-4-((tert-Butoxycarbonyl)amino)cyclopent-2-enecarboxylic acid
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(1S,4R)-Methyl 4-((tert-butoxycarbonyl)amino)cyclopent-2-enecarboxylate
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(1R,4S)-4-((tert-Butoxycarbonyl)amino)cyclopent-2-enecarboxylic acid
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(1S,4R)-4-((tert-Butoxycarbonyl)amino)cyclopent-2-enecarboxylic acid
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cis-4-((tert-Butoxycarbonyl)amino)cyclopent-2-enecarboxylic acid
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tert-Butyl ((1R,4S)-4-(hydroxymethyl)cyclopent-2-en-1-yl)carbamate
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