Home Chemistry Heterocyclic Building Blocks Pyrrolidines 2-Azabicyclo[2.2.1]Heptane
Hydrogenation: Norbornane can be hydrogenated to yield bicyclo[2.2.1]heptane. This reaction typically requires a catalyst like platinum or palladium.
Addition Reactions: Norbornane can undergo addition reactions with electrophiles. For example, it can react with bromine to form the dibrominated derivative.
Bromination and Chlorination: Norbornane can react with bromine or chlorine to form the corresponding brominated or chlorinated derivatives.
Oxidation: Under certain conditions, norbornane can be oxidized to form compounds such as norbornene.
Ring-Opening Reactions: Norbornane can undergo ring-opening reactions under specific conditions. For instance, it can be subjected to nucleophilic attack to open the ring.
Dehydrogenation: At high temperatures and under certain conditions, norbornane can undergo dehydrogenation to form bicyclo[2.2.0]hexane.
Isomerization: Norbornane can isomerize to form other isomers of bicyclic compounds.
Formation of Complexes: Norbornane can form complexes with transition metals, particularly those that have vacant coordination sites.
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Ethyl 2-(2-azabicyclo[2.2.1]heptan-2-yl)acetate
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tert-Butyl 5-hydroxy-2-aza-bicyclo[2.2.1]heptane-2-carboxylate
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tert-Butyl 6-hydroxy-2-azabicyclo[2.2.1]heptane-2-carboxylate
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2-Azabicyclo[2.2.1]heptane hydrochloride
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tert-Butyl 6-amino-2-azabicyclo[2.2.1]heptane-2-carboxylate
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