Home Chemistry Organic Building Blocks Aryls (9H-Fluoren-9-Yl)Methyl (2-(Tritylthio)Ethyl)Carbamate
Hydrolysis:Treatment with aqueous acid or base can lead to the hydrolysis of the carbamate group, yielding the corresponding amine and carbon dioxide.
Nucleophilic Substitution:The tritylthio group can undergo nucleophilic substitution reactions with various nucleophiles (e.g., amines, thiols) to displace the tritylthio group and form new compounds.
Esterification:If exposed to suitable conditions, it can undergo esterification reactions with acids, alcohols, or other nucleophiles, replacing the carbamate group.
Reduction:The carbamate group can be reduced to the corresponding amine using reducing agents such as lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4).
Oxidation:Oxidation of the thioether group to the corresponding sulfoxide or sulfone can occur under specific conditions.
Wittig Reaction:It can undergo a Wittig reaction with suitable reagents to form olefins with the elimination of the carbamate group.
Protection:The carbamate group can be used to protect an amine functionality during chemical transformations and selectively removed when needed.
Cross-Coupling Reactions:The compound can participate in various cross-coupling reactions, such as Suzuki coupling, Heck reaction, or Stille coupling, if the appropriate conditions and reagents are used.
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