Home Chemistry Heterocyclic Building Blocks Pyrrolidines (3Ar,6As)-Octahydrocyclopenta[C]Pyrrole
Hydrogenation: Octahydrocyclopenta[c]pyrrole can undergo hydrogenation reactions, where hydrogen gas (H2
) is added across the double bonds in the molecule. This can lead to the saturation of the double bonds and the formation of cyclopentylpiperidine derivatives.
Amine Reactions: The pyrrole ring in this compound contains a nitrogen atom, which can participate in various amine reactions. For example, it can undergo N-alkylation, N-oxidation, or N-substitution reactions.
Ring Opening Reactions: Depending on the reaction conditions, ring opening reactions can occur, leading to the formation of open-chain compounds.
Cycloaddition Reactions: It can participate in various cycloaddition reactions, such as Diels-Alder reactions or other types of cycloadditions with suitable dienophiles or other reactants.
Substitution Reactions: The compound can undergo substitution reactions, where one or more substituents on the molecule are replaced by other groups or atoms.
Acid-Base Reactions: The compound may undergo acid-base reactions, depending on the presence of acidic or basic functional groups in the molecule.
Esterification or Amidation: If suitable functional groups are present, it can undergo esterification or amidation reactions to form esters or amides.
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rel-(3AR,5r,6aS)-2-(tert-butoxycarbonyl)octahydrocyclopenta[c]pyrrole-5-carboxylic acid
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(1S,3aR,6aS)-Ethyl octahydrocyclopenta[c]pyrrole-1-carboxylate hydrochloride
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(1S,3aR,6aS)-tert-Butyl octahydrocyclopenta[c]pyrrole-1-carboxylate oxalate
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(1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid hydrochloride
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cis-2-(tert-Butoxycarbonyl)octahydrocyclopenta[c]pyrrole-5-carboxylic acid
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