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acetals's Usage Examples:

molecules exist as cyclic hemiacetals that are epimeric ( diastereomeric) to each other.

An example of arylsulfonyl acetals as carbohydrate-protective.

In general these isolable hemithioacetals are cyclic, which disfavors dissociation, and can often be further stabilized by the presence of acid.

The thioacetals are useful in umpolung of carbonyl groups.

condensation polymers include polyamides, polyacetals, and proteins.

are H, and are therefore a subclass of the hemiacetals.

) Aldaric acids cannot form cyclic hemiacetals like unoxidized sugars, but they can sometimes form lactones.

Among its many transformations, it oxidizes methoxyl phenols to quinone acetals, alkenes to acetals, and cyclic alkenes.

In general these isolable hemithioacetals are cyclic, which disfavors dissociation, and can often.

Thioacetals and thioketals feature C−S−C−S−C bond sequence.

list of corticosteroid cyclic ketals, including cyclic ketals (cyclic acetals) of steroidal glucocorticoids and mineralocorticoids.

and formation of acetals possessing atypical properties is achieved by using arylsulfonyl acetals.

a single alcohol has been added to the carbonyl group, in contrast to acetals or ketals, which are formed when a second alkoxy group has been added to.