Examples of 'suzuki reaction' in a sentence
Meaning of "suzuki reaction"
The Suzuki reaction is a chemical process named after its developer, Professor Akira Suzuki, involving the coupling of organoboranes and organic halides
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- The organic reaction of an aryl- or vinyl-boronic acid with an aryl- or vinyl-halide or pseudohalide, such as triflates, catalyzed by a palladium(0) complex, widely used to synthesize polyolefins, styrenes, and substituted biphenyls.
How to use "suzuki reaction" in a sentence
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suzuki reaction
Both materials were synthesized by suzuki reaction and have their structural and photoluminescence properties studied.
The product is a precursor to the Suzuki reaction.
The Suzuki reaction may also be carried out in the reverse manner.
The second step completing tamoxifen is a Suzuki reaction.
Suitable conditions for the Suzuki reaction employ a palladium catalyst.
This reaction has become known as the Suzuki reaction.
The Suzuki reaction is often carried out in mixtures of water and organic solvents.
Extensions of the work involving an in situ Suzuki reaction are presented.
Standard Suzuki reaction conditions are then employed to finally generate the target compounds.
Reaction mixture was used without further work up in following Suzuki reaction.
Such reactions are generally known as a Suzuki reaction and are well known in the art.
This crude mixture was used without further purification or characterization in the subsequent Suzuki reaction.
The Suzuki reaction conditions may vary.
Preferably the reaction is carried out under Suzuki reaction conditions.
Or to a Suzuki reaction according to the conditions described in Synth.
See also
Note that partial hydrolysis of the nitrile group occurs under the Suzuki reaction conditions.
Examples include the Suzuki reaction and Stille reaction.
The BOC group was cleaved under the conditions of the Suzuki reaction.
For the Suzuki reaction.
Dioxaborolane Series is widely used in Suzuki reaction.
The Suzuki reaction is.
DME was introduced as solvent in the Suzuki reaction by Gronowitz.
Suzuki reaction with suitable aryl or heteroaryl halide gives the alcohol ( XVIIa ).
Cyclopropyl or aryl groups can be introduced with the Suzuki reaction N.
Hence, it has been widely used in Suzuki reaction as an organoborane partner.
It is also used in the synthesis of biaryl compounds, such as the Suzuki reaction.
The general conditions for the Suzuki reaction were as follows,.
Suzuki reaction with a suitable aryl or heteroaryl halide yields the ester ( XXVI ).
The latter was then coupled in a Suzuki reaction to give styrenes of formula ( VIII ).
The oxadiazole heterocycle is formed after the carbon-carbon bond formation of the Suzuki reaction.
For illustrative purposes, the Suzuki reaction is employed to couple a boronic ester to an arylbromide.
A particularly useful substitution method employs a palladium catalyzed cross-coupling Suzuki reaction Huff, B. et . al.
The intermediate 3 may react via a Suzuki reaction with the corresponding antenna 21.
The Suzuki reaction was performed on the crude product using a catalyst loading of 0.5 mol %.
Compound 69 can be converted to compound 70 by a Suzuki reaction.
Suzuki reaction Reduction only 1 mol eq.
In some embodiments, the Suzuki reaction includes the use of a base, such as K2CO3.
Suzuki reaction of ( IV ) with a suitable aryl or heteroaryl halide ( A-X ) produces the desired product ( V ).
Subsequent Suzuki reaction of ( VIII ) with a suitable aryl or heteroaryl halide produces ( IX ).
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Examples of using Suzuki
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Suzuki went on a regional tour to promote the films
Sound effects and recording suzuki akira
Suzuki would never do such a stupid thing
Examples of using Reaction
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It would give its reaction at a later date
Quick reaction times in case of delay s or malfunctioning
I am having a physical reaction to how bad this is
