Pyridine is also used as a base in condensation reactions.

This process is the one that usually initiates condensation reactions.

In the related condensation reaction water is released from two different reactants.

In many systems, both protonation and condensation reactions can occur.

As mentioned above, a condensation reaction is also an acid-base reaction.

It is also active in the condensation reaction in heme synthesis.

PbO is used in certain condensation reactions in organic synthesis.

An acyl substitution condensation reaction occurs, with loss of water, forming 3-nitrophthalhydrazide.

Variations to this process are possible using poly(dichlorophosphazene) made by condensation reactions.

Other synthetic methods include the condensation reactions of organic-substituted phosphoranimines.

Its original preparation demonstrated the scope of condensation reactions to construct new, complex organic compounds.

A large number of ketones undergo analogous condensation reactions.

With respect to its condensation reactions, acetaldehyde is prochiral.

Chemically, the polymerization reaction can be seen as a condensation reaction.

The Mannich reaction is also considered a condensation reaction.

PO can be seen as the end product of condensation reactions, where each tetrahedron shares three corners with the others.

This condensation reaction yields the newly formed peptide bond and a molecule of water.

Continuous water removal from condensation reactions such as esterifications to enhance conversion and rate of the reaction.

This condensation reaction is catalyzed by amines such as ammonia and pyridine.

This reaction can be described as a condensation reaction, with two molecules joining together with loss of water.

This is a condensation reaction, meaning water is produced in the reaction as a byproduct.

This can be achieved by a condensation reaction of the diamine with salicylaldehyde as follows:

They are conveniently prepared by condensation reaction of boric acid and the alcohol:

Many biological transformations are condensation reactions.

Next, aspartate undergoes a condensation reaction with carbamoyl-phosphate to form orotic acid.