Home Chemistry Organometallic Reagents Organoboron (2-Chloro-6-Fluorophenyl)Boronic Acid
These compounds have the same murcko framework: benzene,and at least 3 kinds of functional groups( —Cl,—B(OH)2,—F).
Reduction: Chlorobenzene can be reduced to form cyclohexane under certain conditions, often using strong reducing agents like sodium in the presence of 【alcohol|https://www.ambeed.com/alcohols.html】.
Aromatic Substitution Reactions: Phenylboronic acid can undergo nucleophilic aromatic substitution reactions, especially under certain conditions. These reactions can lead to the formation of various functionalized aromatic compounds.
Cross-Coupling Reactions: Fluorobenzene can be utilized in cross-coupling reactions, such as Suzuki-Miyaura, Negishi, and Stille reactions. These reactions involve coupling a halogenated aromatic compound with an organometallic reagent, resulting in the formation of new carbon-carbon bonds.
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(6-Chloro-2,3-difluorophenyl)boronic acid
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2-Chloro-6-fluoro-3-hydroxyphenylboronic acid
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2-Chloro-6-fluoro-3-methoxyphenylboronic acid
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(2,3-Dichloro-6-fluorophenyl)boronic acid
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(3-Bromo-2-chloro-6-fluorophenyl)boronic acid
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2-Chloro-6-fluoro-3-methylphenylboronic acid
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2-Chloro-6-fluoro-5-methylphenylboronic acid
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2-Chloro-3-ethoxy-6-fluorophenylboronic acid
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