Examples of 'tertiary alcohol' in a sentence
Meaning of "tertiary alcohol"
Tertiary alcohol: A type of alcohol compound where the carbon atom bonded to the hydroxyl group (OH) is also bonded to three alkyl groups
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- Any alcohol of general formula R₃C-OH
How to use "tertiary alcohol" in a sentence
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tertiary alcohol
Tertiary alcohol does not undergo oxidation reaction.
This reaction will produce a tertiary alcohol.
Tertiary alcohol groups are unaffected.
Preferred alcohols have secondary or tertiary alcohol groups.
Campholenic tertiary alcohol and its use as a perfuming ingredient.
Particularly preferred ethers are those deriving from a tertiary alcohol.
Other tested heteroaryl tertiary alcohol derivatives were significantly less active.
Preferably the ethers derive from a secondary or tertiary alcohol.
Catalyst for oxidation of olefin or tertiary alcohol and process for production thereof.
An organometallic reagent is then added to this ketone to yield a tertiary alcohol.
Reaction of the isocyanate and the tertiary alcohol provides a urethane.
An additional reaction is to use a Grignard reactant on an ester to obtain a tertiary alcohol.
TLC revealed tertiary alcohol and no olefin.
During early structural investigation the presence of a saturated tricyclic tertiary alcohol was established.
The tertiary alcohol starting material of the formula VI may be obtained as defined hereinbefore.
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The ester reaction with an alkyl Grignard will afford the tertiary alcohol.
Desoxylation of the tertiary alcohol in mazindol improves DAT and SERT binding.
It is preferably an aliphatic or cycloaliphatic, secondary or tertiary alcohol.
The organic solvent is a tertiary alcohol having up to 8 carbon atoms.
In certain embodiments, the solvent is a tertiary alcohol.
Alternatively, an aliphatic tertiary alcohol can be used, preferably tertiary butanol.
In certain aspects, the solvent is a tertiary alcohol.
Deprotection of the tertiary alcohol affords LXX, the isomer of LXI.
The reaction product is a primary, secondary or tertiary alcohol.
In certain aspects, the tertiary alcohol is tert - amyl alcohol.
In certain aspects, the solvent consists of a tertiary alcohol.
In a particular aspect, the tertiary alcohol is tert - amyl alcohol.
In certain embodiments, the solvent consists of a tertiary alcohol.
In certain embodiments, the tertiary alcohol is tert - amyl alcohol.
In preferred embodiments, the alcohol is a secondary or tertiary alcohol.
In a particular embodiment, the tertiary alcohol is tert - amyl alcohol.
In a preferred method, the solvent used is an alcohol, in particular a secondary or tertiary alcohol.
The alcohol can be a primary, secondary or tertiary alcohol or a mixture thereof.
A method as claimed in claim 3 characterised in that the organic complexing agent is a tertiary alcohol.
Composition according to claim 8 wherein the tertiary alcohol has more than 5 carbon atoms.
As obvious from the list, the alcohol can be primary, secondary or tertiary alcohol.
In some cases, the ketone, secondary, and tertiary alcohol were isolated and characterized.
In one embodiment the ethers are acyclic and derive from a primary, secondary or tertiary alcohol.
A higher alcohol may be a primary, secondary or tertiary alcohol having 12 or more carbon atoms.
The methanol-water separation is done in a distillation column with a side draw to remove tertiary alcohol.
The resulting tertiary alcohol can then be purified by column chromatography ( hexanes / ethyl acetate ).
The hydroxyl group may be a primary, secondary or tertiary alcohol group.
The tertiary alcohol furan was purified using flash column chromatography with 6:1 hexane / ethyl acetate.
In certain embodiments, the solvent consists of the tertiary alcohol as defined above.
Also, the tertiary alcohol is denatured for use in anti ‑ freeze, window ‑ cleaning fluid and methylated spirit.
Reaction with pentafluoroethyl lithium produces the complete side chain, the tertiary alcohol XIId.
The crude tertiary alcohol was passed through a plug of SiO2 ( DCM ) to give a yellow solid.
The reaction mixture was examined by LC-MS which showed the complete formation of tertiary alcohol.
Preferred acids for dehydration of the tertiary alcohol include p-TsOH and H2SO4.
Treatment of the ketone with a suitable organometallic reagent provides the tertiary alcohol A54.
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