secondary amine

It can also be made to react with secondary amines.

It is also a good test for the successful deprotection of a secondary amine.

Compared to acyclic secondary amines, it is about 10 times more basic.

By the end of this step a secondary amine, the base of the drug, is formed.

Sometimes it is also used for the analogous derivatives of primary and secondary amines.

Chloranil is used to test for free secondary amines.

The test turns blue for some secondary amines.

Where possible, don't use metalworking fluids that contain secondary amines.

This is the converted to the secondary amine (4) by treatment with aqueous base.

A more recent development is the use of chiral secondary amine catalysts.

Proline is the only amino acid with a secondary amine.

It is also a secondary amine like methamphetamine, and forms salts in the same way.

Hydrogen bonding significantly influences the properties of primary and secondary amines.

A secondary amine in the same reaction will directly form an insoluble sulfonamide.

Conjugated carbonyls react with secondary amines to form 3-aminocarbonyls (3-ketoamines).

For some applications, the primary and secondary amines are often subjected to the Leuckart reaction.

Metabolism of other 1-methylated-ergoloids to their secondary amine derivatives has been frequently noted in mammals.

This group can be regarded as a secondary amine with a cyano substituent.

The organic function is a primary or secondary amine:

A strategy for the protection and deprotection of sensitive secondary amines is based on this principle.

Secondary amines can also be prepared by in situ formation of N-chloramines.

The molecule is a secondary amine with two picolyl substituents.

It is a cyclic secondary amine, also classified as a saturated heterocycle.

Diethanolamine is polyfunctional, being a secondary amine and a diol.

Classified as a secondary amine, it is derived from isoquinoline by hydrogenation.