Examples of 'thiols' in a sentence
Meaning of "thiols"
Thiol: a compound that contains the functional group -SH, resembling alcohol but containing sulfur instead of oxygen. Thiols are found in onions and garlic and are often used in organic synthesis
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- plural of thiol
How to use "thiols" in a sentence
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thiols
Not all thiols have unpleasant odors.
A multifunctional thiol can be a mixture of different thiols.
Thiols are readily alkylated to give thioethers.
Reactivity towards thiols for different enes.
Thiols sometimes are also called sulfhydryls or mercaptans.
Other nucleophiles include thiols such as mercaptoethanol.
Conjugating the drug to the interchain thiols.
A wide range of organic thiols are commercially available.
Thiols can be protected by a trityl group.
Examples of strong nucleophiles are thiols and amines.
Hours for thiols under argon.
Example of reactivity of different thiols and enes.
The preferred aliphatic thiols are dodecanethiol and terdodecanethiol.
They are not as odoriferous as the thiols.
Secondary and tertiary thiols are less easily prepared.
See also
These thiols can be used a nucleophiles to as discussed above.
Disulfides can be reduced to thiols by a variety of enzymatic processes.
These include cyanohydrins and thiols.
The excess of thiols are washed away.
Sulfides are typically prepared by alkylation of thiols.
The relevant thiols are given in the table below.
Other frequently used stabilisers are thiols.
The amount of free thiols is determined.
Presently preferred reagents are phosphine compounds and thiols.
Disulfides reduce to thiols via thiolates.
Of particular interest in this invention as strong nucleophiles are thiols.
Many thiols have strong odors resembling that of garlic.
Suitable donors described are ethoxylated pentaerythritol and thiols.
Thiols are sometimes referred to as mercaptans.
These compounds have been used to carboxymethylate free thiols.
These thiols give pronounced exotic fruit or citrus notes.
Examples of sulfur compounds are thiols or polythiols.
The reactivity of thiols is in many respects similar to that of alcohols.
Preferred reducing agents are free thiols.
Thiols are very generally used as reducing agents in reducing compositions.
Thioketals can be obtained by reacting ketones or aldehydes with thiols.
Thiols offer another approach.
It belongs to the group of thiols.
Thiols are also referred to as mercaptans.
They are prepared by condensation of thiols or dithiols with aldehydes.
Thiols are effective nucleophiles for substitution at saturated carbon atoms.
Antioxidants may include reducing agents such as thiols or polyphenols.
Thiols have a lower dipole moment relative to the corresponding alcohol.
There are no existing anticancer agents which deplete cellular thiols.
The blond is from oxidized thiols evident in the hair shaft.
Illustrative examples of suitable nucleophiles include hydrazides and thiols.
The blonde is from oxidized thiols evident in the hair shaft.
The disulfide is cleaved by thiols.
The thiols are then reduced with dithiothreitol and labelled by monobromobimane.
Strong odor is common in creams that have thiols as a base.
