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Synonym Chemical Name(s) for 4-(2-carboxyethyl)phenylboronic acid

For background to the synthesis, structures and applications of phenylboronic acid derivatives, see: Barba & Betanzos (2007); Barba (2004, 2006); Bernstein (1995); Christinat (2008); Dreos (2002); Fujita (2008); Höpfl (2002); Hall (2005); Lulinski (2007); Miyaura & Suzuki (1995); Severin (2009); Shinkai (2001); Smith (2008); Zhang (2007).

Your search results for 4-Isobutylbenzeneboronic acid, 98%

3-Aminophenylboronic acid monohydrate is a commercially available product that has been crystallized from a solvent mixture of benzene, methanol and water to generate colourless blocks of (I); M.p. 368 K.

V., Synthesis of (azidomethyl)phenylboronic acids.

Phenylboronic acid is white powder and is commonly used in organic synthesis

Substituted phenylboronic acid derivatives have been prepared mainly for applications in organic synthesis (Miyaura & Suzuki, 1995; Hall, 2005) and for molecular recognition of biochemically active molecules (Shinkai , 2001). More recently, such boronic acid derivatives have attracted attention also as building blocks for the self-assembly of macrocyclic and polymeric assemblies. For this purpose, the boronic acid is generally converted to an ester (boronate) via condensation with an aliphatic or aromatic diol, which is then assembled to a macromolecular structure via reaction of the additional attached to the -phenyl ring (Höpfl, 2002; Fujita , 2008; Severin, 2009). In this context, 3-aminophenylboronic acid has been employed for the generation of macrocycles and cages (Dreos , 2002; Barba , 2004 and 2006; Barba & Betanzos, 2007; Christinat , 2008).

Substituted phenylboronic acid derivatives have been prepared mainly for applications in organic synthesis (Miyaura & Suzuki, 1995; Hall, 2005) and for molecular recognition of biochemically active molecules (Shinkai , 2001). More recently, such boronic acid derivatives have attracted attention also as building blocks for the self-assembly of macrocyclic and polymeric assemblies. For this purpose, the boronic acid is generally converted to an ester (boronate) via condensation with an aliphatic or aromatic diol, which is then assembled to a macromolecular structure via reaction of the additional attached to the -phenyl ring (Höpfl, 2002; Fujita , 2008; Severin, 2009). In this context, 3-aminophenylboronic acid has been employed for the generation of macrocycles and cages (Dreos , 2002; Barba , 2004 and 2006; Barba & Betanzos, 2007; Christinat , 2008).

Arylboronic acid or boronate synthesis - Organic …

Synthesis of arylboronic acids and ..

For background to the synthesis, structures and applications of phenylboronic acid derivatives, see: Barba & Betanzos (2007); Barba (2004, 2006); Bernstein (1995); Christinat (2008); Dreos (2002); Fujita (2008); Höpfl (2002); Hall (2005); Lulinski (2007); Miyaura & Suzuki (1995); Severin (2009); Shinkai (2001); Smith (2008); Zhang (2007).

A Convenient Synthesis of 1,4,5-Trisubstituted 1,2,3-Triazoles via 1,3-Dipolar Cycloaddition/Coupling of Alkynes, Phenylboronic Acids, and Sodium Azide Catalyzed by Cu(I)/Cu(II).

LiCl enables the synthesis of various aryl boronic acids in a ..
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Search results for benzene boronic acid at Sigma-Aldrich

For background to the synthesis, structures and applications of phenyl­boronic acid derivatives, see: Barba & Betanzos (2007); Barba (2004, 2006); Bernstein (1995); Christinat (2008); Dreos (2002); Fujita (2008); Höpfl (2002); Hall (2005); Lulinski (2007); Miyaura & Suzuki (1995); Severin (2009); Shinkai (2001); Smith (2008); Zhang (2007).

Synthesis of Aromatic Boronic Acids

4-(2-carboxyethyl)benzeneboronic acid
4-(2-carboxyethyl)benzene boronic acid
3-(4-dihydroxyborylphenyl)propanoic acid
3-(4-dihydroxyborylphenyl)propionic acid
3-[4-(dihydroxyboryl)phenyl]propanoic acid
3-[4-(dihydroxyboranyl)phenyl]propanoic acid

Benzene Substitutions|Heterocyclics|Boronic Acid ..

Boronic acids are alkyl or aryl substituted boric acids containing a carbon-boron bond and represented by R-B(OH)2. Generally, boronic acids act as Lewis acids. Boronic acid can easily form reversible covalent complexes with sugars, amino acids, and hydroxamic acids. Owing to its low toxicity and relatively quick degradation in the environment, boronic acid is considered as a “green” compound. During dehydration, boronic acids give the corresponding boronic anhydrides or boroxines. A six membered heterocyclic ring comprising alternate oxygen and boron atoms is referred to as a boroxine. Boroxines are the cyclotrimeric anhydrides of boronic acids, and isoelectronic to benzene. Examples of boronic anhydrides include trimethylboroxine and triphenylboroxine. Boronic acids and their corresponding boronic anhydrides exist in equilibrium at room temperature.

Boronic acid is a mild organic Lewis acid; their reactivity, stability, and ease of handling have caused them to be significant synthetic intermediates. Boronic acids are often employed in synthetic organic chemistry in the Suzuki reaction, for Chan-Lam coupling, for Liebeskind–Srogl coupling, for forming carbon-carbon bonds, carbon-nitrogen bonds, and carbon-oxygen bonds. In supramolecular chemistry, boronic acid is used for the recognition of molecules binding to saccharides and for the fluorescent detection, or selective transport, of saccharides across membranes. Boronic anhydrides are widely used in the production of optics. One of the most common boronic anhydrides used in the methylation of aryl halides by palladium-catalyzed Suzuki-Miyaura coupling reactions is trimethylboroxine. Owing to the presence of covalent chemistry in the boroxine ring, boronic anhydrides find their use in novel molecular architectures and functional materials (Review: Boroxine chemistry and applications: A perspective. Korich, A. L. Dalton Trans., 2010, 39, 1423-1431.

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