Home Chemistry Organometallic Reagents Organoboron Benzyl (4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl)Carbamate
Suzuki-Miyaura Coupling: Boronic esters can react with aryl or vinyl halides in the presence of a palladium catalyst and a base to form new carbon-carbon bonds. This is a widely used method for synthesizing biaryl compounds.
Hydrolysis: Boronic esters can be hydrolyzed under acidic or basic conditions to produce the corresponding boronic acid and alcohol. This reaction can be useful for isolating or purifying boronic acids.
Oxidation: Boronic esters can be oxidized to boronic acids using reagents like hydrogen peroxide or peroxy acids.
Halogenation: Boronic esters can be halogenated at the boron center, leading to the formation of new carbon-boron bonds. This can be useful in the synthesis of various organic compounds.
Reductive Transformations: Boronic esters can undergo reductive transformations to convert them into other functional groups, such as boronate esters, which can be useful in various synthetic processes.
Cross-Coupling Reactions: Boronic esters can participate in various cross-coupling reactions other than Suzuki-Miyaura coupling, such as Stille coupling and Kumada coupling, depending on the reactants and conditions.
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Benzyl propyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate
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Benzyl (4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate
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Benzyl (3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate
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Benzyl butyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate
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Benzyl (2-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate
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