Examples of 't-butyl' in a sentence
Meaning of "t-butyl"
t-butyl is a noun referring to a chemical compound where the t- represents a tertiary butyl group. It is commonly used in organic chemistry to describe a molecular structure
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- Synonym of tertiary butyl
How to use "t-butyl" in a sentence
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t-butyl
The use of t-butyl alcohol as a solvent is mentioned.
Examples of such groups are methyl and t-butyl.
Two equivalents of potassium t-butyl hydroxide were added.
Preferred alkyl radicals are methyl and t-butyl.
Alkyllithium reactants such as t-butyl lithium are preferred.
The most preferred protecting group is t-butyl.
If the substituent is t-butyl nitroxide no metal complexes are formed.
Examples of the hydroperoxides include t-butyl hydroperoxide.
The t-butyl oligomers are loosely organized on the surface.
The residue was dissolved in t-butyl methyl ether.
The t-butyl esters are hydrolyzed with trifluoroacetic acid.
A preferred free radical initiator is t-butyl hydroperoxide.
X represents t-butyl group from initiator.
The protective group is preferably a t-butyl group.
The t-butyl esters were deprotected with trifluoroacetic acid.
See also
Aqueous was extracted with methyl t-butyl ether.
Removal of the t-butyl ester linkage with p TsOH.
A particularly preferred curing agent is t-butyl perbenzoate.
The t-butyl oligomers arc loosely organized on the surface.
The most preferred hydroperoxide is t-butyl hydroperoxide.
Use of t-butyl ether as a protecting group fulfills these requirements.
An example of such an alkylating agent is t-butyl chloroacetate.
T-butyl hydroperoxide is especially useful.
It is preferred that t-butyl acetate be used.
Isobutene can be usefully converted to methyl t-butyl ether.
Suitable monomers include t-butyl amino ethyl acrylate or methacrylate.
Examples include methyl hypochlorite and t-butyl hypochlorite.
Both ethyl and t-butyl esters gave similar results.
This process can be moderated by using t-butyl solvent.
Use of t-butyl peresters will result in ether or alkane endgroups.
The formed enol is trapped as a t-butyl dimethylsylane derivative.
Lower alkyl is preferably methyl or t-butyl.
Polymerisation was effected using t-butyl hydroperoxide and isoascorbic acid.
A specific example of an unsuitable monomer type is t-butyl styrene.
Examples of such compounds are t-butyl chromate and chromium acetylacetonate or acetate.
Advantageously this is a methyl or t-butyl group.
Hydroperoxides such as t-butyl and cumyl hydroperoxides may also be used.
The initiator is peroxide or hydroperoxide such as t-butyl hydroperoxide.
T-butyl and other carboxylic acid protecting groups are especially preferred.
The mixture was extracted with methyl t-butyl ether.
Examples of these materials include t-butyl hydroperoxide and cumene hydroperoxide.
It was then extracted twice with methyl t-butyl ether.
Cumene hydroperoxide, t-butyl hydroperoxide and diisopropyl benzene hydroperoxide are preferred.
Preferred solvents are toluene and t-butyl methyl ether.
Both t-butyl hydroperoxide and ethylbenzene hydroperoxide can be used as oxygen sources.
Specific examples of the peroxycarbonates include t-butyl peroxyisopropylcarbonate.
Removal of the t-butyl group from the aspartyl residue yields eptifibatide.
To these portions various amounts of t-butyl catechol was added.
Examples of branched alkyl groups include isopropyl and t-butyl.
To the solution was added t-butyl hydroperoxide.
