Home Chemistry Heterocyclic Building Blocks Carbazole Series 2,3,4,9-Tetrahydro-1H-Carbazol-1-One
Acylation: You can react it with acyl chlorides or anhydrides to form N-acyl derivatives.
Reduction: The carbonyl group (C=O) in the compound can be reduced to the corresponding alcohol using reducing agents like sodium borohydride (NaBH4) or lithium aluminum hydride (LiAlH4).
Amination: You can introduce amine groups by reacting it with primary or secondary amines under suitable conditions.
Alkylation: You can alkylate the nitrogen atom in the compound using alkyl halides or alkyl sulfonates.
Cyclization: Depending on the reaction conditions, it may undergo cyclization reactions to form various cyclic compounds.
Oxidation: The compound can be oxidized under appropriate conditions to convert the alcohol group (if present) into a carbonyl group or other oxidation products.
Substitution Reactions: Depending on the reagents and conditions, various substitution reactions can occur, including nucleophilic aromatic substitution or other substitution reactions at reactive positions.
Cycloaddition Reactions: Depending on the structure and reagents, it may participate in cycloaddition reactions, such as Diels-Alder reactions.
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8-Methyl-2,3,4,9-tetrahydro-1H-carbazol-1-one
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6-Methoxy-2,3,4,9-tetrahydro-1H-carbazol-1-one
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6-Chloro-2,3,4,9-tetrahydro-1H-carbazol-1-one
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6-Methyl-2,3,4,9-tetrahydro-1H-carbazol-1-one
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6-Bromo-2,3,4,9-tetrahydro-1H-carbazol-1-one
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8-Bromo-2,3,4,9-tetrahydro-1H-carbazol-1-one
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