Home Chemistry Organic Building Blocks Esters (9H-Fluoren-9-Yl)Methyl (3-Phenylpropyl)Carbamate
Hydrolysis: Under acidic or basic conditions, carbamates like this one can undergo hydrolysis, leading to the formation of the corresponding amine and alcohol. In this case, it would yield "(9H-fluoren-9-yl)methylamine" and "3-phenylpropanol."
Grignard Reaction: If you have a suitable electrophilic center in the molecule, you can perform Grignard reactions to introduce various substituents.
Reduction: The carbamate can be reduced to the corresponding amine using reducing agents like lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4).
Oxidation: Depending on the reaction conditions and the presence of other functional groups, oxidation reactions may be possible.
Nucleophilic Substitution: If there are suitable leaving groups or electrophilic sites in the molecule, it may undergo nucleophilic substitution reactions.
Wittig Reaction: If a carbonyl group is present, you could perform a Wittig reaction to introduce an alkene.
Heck Reaction: If there's a suitable halide or other leaving group, a Heck reaction could be employed to form a carbon-carbon bond.
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Fmoc-(S)-3-amino-2-benzylpropanoic acid
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