Examples of 'acetals' in a sentence
Meaning of "acetals"
Acetal is a type of organic compound often used in industrial processes
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- plural of acetal
How to use "acetals" in a sentence
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acetals
Acetals are products of substitution reactions catalyzed by acid.
Alkoxylated glycerol acetals and their derivatives.
Hemiacetals react with alcohols to form acetals.
Diesel fuel compounds containing glycerol acetals.
They form acetals with the benzaldehyde.
Silyl ethers or alkyl ethers and acetals.
It also rapidly forms an acetals in the presence of alcohols.
Forming germicidal aromatic dialdehydes with acetals.
The acetals may be present in the mixture as an impurity.
Examples of suitable dialkyl acetals include benzoyloxyacetaldehyde dialkyl.
Acetals as protecting groups and thioacetals.
The synthesis of acetals is a reversible reaction.
These do not form as readily as hemiacetals and acetals.
Thioacetals are the sulfur analogues of acetals.
Process for preparing halo acetals from enamines.
See also
Acetals convert to carbonyl compounds.
Examples of unstable functionalities include acetals and ketals.
The acetals may be used alone or in a combination of the plural.
Aldehyde protecting groups include acetals and hemiacetals.
Polyvinyl acetals are particularly preferred.
Also mixtures of the above acetals can be used.
Acetals are decomposed to olefins and alcohols in the presence of an acid.
Methylal will be preferred as acetals.
Acetals are used as protecting groups.
The derivatising groups are derived from acetals and aldehydes.
Acetals tend to be more stable toward oxidation than dialdehydes.
Limonene gives the corresponding acetals in high yields in both systems.
Polyacetals can also be prepared by the polymerization of cyclic acetals.
These acid solids adsorb preferentially water rather than acetals.
Suitable polyacetals may also be prepared by polymerizing cyclic acetals.
Agrochemical compositions comprising alkoxylated glycerol acetals and their derivatives.
These acetals were evaluated as chiral auxiliaries for use in asymmetric synthesis.
Ozone reacts very smoothly with acetals to give the corresponding esters.
Acetals and ketals.
Polyoxymethylene compounds and polymeric acetals prepared from formaldehyde and polyols.
Acetals are well known to be hydrolytically labile under mildly acidic conditions.
Process for preparing cyclic acetals which can be used as fuel components.
The acetals used in the invention have attractive fragrance characteristics.
Aluminium hydride can be used in the reduction of acetals to half protected diols.
The acetals and ketals can be removed with mild acids.
Suitable reactive derivatives of aldehydes and ketones include acetals and ketals.
Suitable polyacetals may also be obtained by the polymerization of cyclic acetals.
One or more catalysts for the hydrolysis of amide acetals may be present.
Cyclic acetals and ketals were converted by this reagent into hydroxy ethers.
The scope of the invention is not limited to just these types of acetals.
The diketene acetals may also be prepared by the isomerization of divinyl acetals.
The diols used to prepare the oligomeric acetals of this invention are of several types.
Acetals are stable compared to hemiacetals but their formation is a reversible equilibrium as with esters.
These results are interpreted in terms of a conformational change before oxidation in the acyclic acetals.
Such ketals and acetals are well known blocking groups in saccharide chemistry.
