Examples of 'alkyne' in a sentence
Meaning of "alkyne"
An alkyne is a hydrocarbon compound containing carbon-carbon triple bonds
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- A hydrocarbon containing at least one carbon–carbon triple bond.
How to use "alkyne" in a sentence
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alkyne
Phenylacetylene is an alkyne hydrocarbon containing a phenyl group.
Generally the substrate will be an alkene or alkyne.
A preferred such alkyne protecting group is trimethylsilyl.
In alkene radicals proton abstraction to an alkyne is preferred.
Examples of the alkyne include acetylene and phenylacetylene.
Those containing triple bonds are called alkyne.
The alkyne compound is described below.
Purification by chromatography gives the desired alkyne.
An alkyne is one of the four main types of hydrocarbons.
Alkynyl moieties contain at least one alkyne.
The alkyne was stored as a light yellow solution in toluene.
It is a hydrocarbon and the simplest alkyne.
Catalyst and alkyne hydrogenation process.
Formal cycloadditions also take place in alkyne trimerisation.
Reaction of an alkyne with an azide to form a triazole is illustrated.
See also
Butynediol is an organic compound that is an alkyne and a diol.
When the substrate is an alkyne the reaction product is a vinylorganometallic.
Oxidative demetallation gives the desired alkylated alkyne.
The presently preferred alkyne is acetylene.
Mixture of at least one olefin and one alkyne.
Azide alkyne huisgen cycloaddition.
The reaction between norbornadiene and an activated alkyne is a cycloaddition.
The alkyne is optionally silylated.
The term is a contraction of the terms alkene and alkyne.
An example of an alkyne group is acetylenyl.
Some acids like tariric acid contains an alkyne group.
Monofunctional alkyne monomers are typically liquids having a relatively low viscosity.
It is the simplest stable alcohol containing an alkyne functional group.
Alkyne metathesis is an organic reaction involving the redistribution of alkyne chemical bonds.
The universal primer can comprise an azide or alkyne moiety.
Some drops of alkyne added to this mixture cause this colour to appear.
One preferred multiple bond compound comprises an alkyne compound.
With a substituted alkyne instead of a terminal alkyne the allene product is favoured.
Usually two equivalents of sodium amide yields the desired alkyne.
T is a group generating a carbanion at a terminal alkyne such as lithium or magnesium bromide.
The molecule consists of phenyl groups attached to both ends of an alkyne.
Alkyne groups may have more than one such multiple bond.
Preferred derivatised surfaces are modified with one or more alkyne groups.
The terminal alkyne can be installed by a variety of methods know in the art.
Repeat the previous step as needed until the alkyne is consumed.
Alkene and alkyne metathesis vía these metal complexes has been studied extensively.
The functional group known to have click reactivity may be an alkyne.
This anomaly is due to the presence of alkyne precursor in the formulated product.
Ynolates are chemical compounds with a negatively charged oxygen attached to an alkyne functionality.
This alkyne function allowed the incellulo click reaction between a fluorescentprobe or a biotin.
This is an alkyne.
Reaction with a disubstituted alkyne with trifluoroacetic anhydride can give a mixture of regioisomers.
It can also be a mixture of at least one olefin and at least one alkyne.
Triazole derivatives can be prepared by reaction of an alkyne compound and trimethylsilyl azide.
Among alkyne groups can be cited for instance acetylene and cyclooctyne groups.
