Home Chemistry Organic Building Blocks Aliphatic Cyclic Hydrocarbons Bicyclo[2.2.1]Heptane
Hydrogenation: Norbornane can undergo catalytic hydrogenation to form decalin (decahydronaphthalene) by breaking the bridgehead double bond. This is a common reaction and is often used to illustrate the concept of ring strain.
Bromination: Norbornane can undergo bromination at the bridgehead carbon atoms. The reaction typically requires strong conditions, and it can lead to the formation of various brominated norbornane derivatives.
Ring Opening: Norbornane can undergo ring-opening reactions under specific conditions. For example, it can be ring-opened to form norbornene using strong acids or other appropriate reagents.
Rearrangements: In some cases, rearrangement reactions can be initiated to convert norbornane into other related compounds. For example, in the presence of Lewis acids, it can undergo a [2+2] cycloaddition with olefins to form various products.
Substitution Reactions: Norbornane can undergo substitution reactions under appropriate conditions. For instance, it can react with electrophiles to form substituted derivatives.
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Bicyclo[2.2.1]heptane-1-carboxylic acid
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Bicyclo[2.2.1]heptane-2,3-dicarboxylic acid
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Boc-2-aminobicyclo[2.2.1]heptane-2-carboxylicacid
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Methyl 4-aminobicyclo[2.2.1]heptane-1-carboxylate
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