Examples of 'phenylboronic acid' in a sentence
Meaning of "phenylboronic acid"
phenylboronic acid: Phenylboronic acid is a chemical compound commonly used in organic synthesis and pharmaceutical research as a building block or reagent
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- The simplest aryl boronic acid, C₆H₅B(OH)₂.
How to use "phenylboronic acid" in a sentence
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phenylboronic acid
Numerous methods exist to synthesize phenylboronic acid.
Phenylboronic acid is used in numerous cross coupling reactions.
There are numerous methods to synthesize phenylboronic acid.
Phenylboronic acid is three times as strong an acid as boric acid.
The preferred arylboronic acid is phenylboronic acid.
Phenylboronic acid is white powder and is commonly used in organic synthesis.
The trimeric anhydrides of phenylboronic acid are called boroxines.
The yield of isolated product depends on the quantity of phenylboronic acid used.
Phenylboronic acid can be selfcondensed to the cyclic trimer called triphenyl anhydride or triphenylboroxin.
This polyanion reagent consists of phenylboronic acid coupled to polyacrylic acid.
Both compounds are condensation products of bis ( hydroxyalkyl ) nitrones and phenylboronic acid.
Suzuki coupling of bromoaryl ether with phenylboronic acid gave the biphenyl ether.
The dehydration of boronic acids gives boroxines, the trimeric anhydrides of phenylboronic acid.
Accordingly, the binding of carbohydrates to phenylboronic acid is weak under physiological conditions.
The composition of claim 1, wherein the tissue adsorbing polymer comprises phenylboronic acid.
See also
Block copolymer having phenylboronic acid group introduced therein, and use thereof.
This method was generalized to a route producing biaryls by coupling phenylboronic acid with aryl halides.
Phenylboronic acid increased the half-life of the CocE the most, followed by benzoic acid.
In some embodiments, the boronic acid is phenylboronic acid.
The resulting phenylboronic acid derivative is referred to in Scheme 3 as compound VIA.
Exemplary of suitable boron compounds are boric acid, phenylboronic acid and isopropylboronic acid.
Phenylboronic acid was also extracted with 3-pentanone with comparable results.
In some embodiments, the boronic acid is isobutyl boronic acid, phenylboronic acid or boric acid.
Phenylboronic acid semiconjugates as previously defined, of formula XV ;.
C-C bond forming processes commonly use phenylboronic acid as a reagent.
The preferred reagents include trimethylboroxine, tri-n-butylboroxine, triphenylboroxine, methylboronic acid, butylboronic acid and phenylboronic acid.
The cartridge contains coupled phenylboronic acid adsorbed to a support 18.
The process according to claim 13, wherein the recovered boronic acid is phenylboronic acid.
Disubstituted phenylboronic acid compound of the following structural formula ( I ),.
Is added, then the solution of boronic acid phenylboronic acid for Ex.
Phenylboronic acid reagents as previously defined, e.g. of formula XIV ; and.
Condensation of equimolar amounts of salicylaldehyde, N-hydroxypiperidine, and phenylboronic acid yields the title compound.
Phenylboronic acid cross-linking reagents as previously defined, e.g. of formulae XII, XVI and XVII.
The final compound [ C ] resulting from this practice show that phenylboronic acid content is acceptable.
Example 45C Example 45B and phenylboronic acid were processed as in Example 21 to provide the designated compound.
Analysis of WT CocE in the presence of 5x molarity phenylboronic acid FIG.
Complete modification of 8arm PEG amines with phenylboronic acid was confirmed by 1H NMR spectroscopy ( Figure 1 ).
Remarkably low catalyst loadings could be used for the cross-coupling of 4 ' - bromoacetophenone with phenylboronic acid.
Most preferably, trimethyl boroxine, tri-n-butylboroxine and phenylboronic acid are used as the reagents.
Examples of the above-mentioned " boron compound corresponding to R8 " include trimethylboroxin, phenylboronic acid.
The boronic diester was formed using another model system, phenylboronic acid ( an analogue of Bortezomib ).
Subsequent treatment with B ( OCH3 ) 3 and HCI results in an ortho-substituted phenylboronic acid.
Example of a compound represented by the formula, R1-B ( OH ) 2 includes phenylboronic acid or the like.
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